241 results on '"Zhao, W."'
Search Results
2. Observation of supersymmetry and its spontaneous breaking in a trapped ion quantum simulator
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Cai, M.-L., Wu, Y.-K., Mei, Q.-X., Zhao, W.-D., Jiang, Y., Yao, L., He, L., Zhou, Z.-C., and Duan, L.-M.
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- 2022
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3. Observation of a quantum phase transition in the quantum Rabi model with a single trapped ion
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Cai, M.-L., Liu, Z.-D., Zhao, W.-D., Wu, Y.-K., Mei, Q.-X., Jiang, Y., He, L., Zhang, X., Zhou, Z.-C., and Duan, L.-M.
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- 2021
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4. Anomalous twin boundaries in two dimensional materials
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Rooney, A. P., Li, Z., Zhao, W., Gholinia, A., Kozikov, A., Auton, G., Ding, F., Gorbachev, R. V., Young, R. J., and Haigh, S. J.
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- 2018
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5. Synthetic lethality between androgen receptor signalling and the PARP pathway in prostate cancer
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Asim, M, Tarish, F, Zecchini, HI, Sanjiv, K, Gelali, E, Massie, CE, Baridi, A, Warren, AY, Zhao, W, Ogris, C, McDuffus, L-A, Mascalchi, P, Shaw, G, Dev, H, Wadhwa, K, Wijnhoven, P, Forment, JV, Lyons, SR, Lynch, AG, O'Neill, C, Zecchini, VR, Rennie, PS, Baniahmad, A, Tavaré, S, Mills, IG, Galanty, Y, Crosetto, N, Schultz, N, Neal, D, Helleday, T, University of St Andrews. School of Medicine, University of St Andrews. Statistics, University of St Andrews. Population and Behavioural Science Division, and University of St Andrews. Cellular Medicine Division
- Subjects
Male ,RC0254 Neoplasms. Tumors. Oncology (including Cancer) ,Science ,~DC~ ,NDAS ,Collagen Type XI ,Article ,RC0254 ,Prostatic Neoplasms, Castration-Resistant ,SDG 3 - Good Health and Well-being ,Receptors, Androgen ,Journal Article ,Humans ,lcsh:Q ,BDC ,Homologous Recombination ,Synthetic Lethal Mutations ,lcsh:Science ,R2C ,Signal Transduction - Abstract
Emerging data demonstrate homologous recombination (HR) defects in castration-resistant prostate cancers, rendering these tumours sensitive to PARP inhibition. Here we demonstrate a direct requirement for the androgen receptor (AR) to maintain HR gene expression and HR activity in prostate cancer. We show that PARP-mediated repair pathways are upregulated in prostate cancer following androgen-deprivation therapy (ADT). Furthermore, upregulation of PARP activity is essential for the survival of prostate cancer cells and we demonstrate a synthetic lethality between ADT and PARP inhibition in vivo. Our data suggest that ADT can functionally impair HR prior to the development of castration resistance and that, this potentially could be exploited therapeutically using PARP inhibitors in combination with androgen-deprivation therapy upfront in advanced or high-risk prostate cancer., Tumours with homologous recombination (HR) defects become sensitive to PARPi. Here, the authors show that androgen receptor (AR) regulates HR and AR inhibition activates the PARP pathway in vivo, thus inhibition of both AR and PARP is required for effective treatment of high risk prostate cancer.
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- 2017
6. Biological recognition of graphene nanoflakes
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Castagnola, V., primary, Zhao, W., additional, Boselli, L., additional, Lo Giudice, M. C., additional, Meder, F., additional, Polo, E., additional, Paton, K. R., additional, Backes, C., additional, Coleman, J. N., additional, and Dawson, K. A., additional
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- 2018
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7. Strain-controlled magnetic domain wall propagation in hybrid piezoelectric/ferromagnetic structures
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Lei, N., Devolder, T., Agnus, G., Aubert, P., Daniel, L., Kim, J. -V, Zhao, W., Trypiniotis, Theodossis, Cowburn, R. P., Chappert, C., Ravelosona, D., Lecoeur, P., ICHAMS - Equipe Interaction Champs - Matériaux et Structures, Laboratoire de génie électrique de Paris (LGEP), Université Paris-Sud - Paris 11 (UP11)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Ecole Supérieure d'Electricité - SUPELEC (FRANCE)-Centre National de la Recherche Scientifique (CNRS)-Université Paris-Sud - Paris 11 (UP11)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Ecole Supérieure d'Electricité - SUPELEC (FRANCE)-Centre National de la Recherche Scientifique (CNRS), and Université Paris-Sud - Paris 11 (UP11)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Ecole Supérieure d'Electricité - SUPELEC (FRANCE)-Centre National de la Recherche Scientifique (CNRS)
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geometry ,Materials science ,Kerr effect ,Magnetoresistance ,Magnetic domain ,General Physics and Astronomy ,magnetic field ,anisotropy ,02 engineering and technology ,electronic equipment ,Bioinformatics ,01 natural sciences ,7. Clean energy ,Article ,General Biochemistry, Genetics and Molecular Biology ,Condensed Matter::Materials Science ,0103 physical sciences ,energy efficiency ,010302 applied physics ,magnetic anisotropy ,Multidisciplinary ,hybrid ,piezoelectricity ,Spintronics ,Magnetic logic ,business.industry ,electronics ,article ,integrated circuit ,Magnetostriction ,General Chemistry ,021001 nanoscience & nanotechnology ,electric field ,Magnetic anisotropy ,Domain wall (magnetism) ,nanowire ,Optoelectronics ,0210 nano-technology ,business - Abstract
The control of magnetic order in nanoscale devices underpins many proposals for integrating spintronics concepts into conventional electronics. A key challenge lies in finding an energy-efficient means of control, as power dissipation remains an important factor limiting future miniaturization of integrated circuits. One promising approach involves magnetoelectric coupling in magnetostrictive/piezoelectric systems, where induced strains can bear directly on the magnetic anisotropy. While such processes have been demonstrated in several multiferroic heterostructures, the incorporation of such complex materials into practical geometries has been lacking. Here we demonstrate the possibility of generating sizeable anisotropy changes, through induced strains driven by applied electric fields, in hybrid piezoelectric/spin-valve nanowires. By combining magneto-optical Kerr effect and magnetoresistance measurements, we show that domain wall propagation fields can be doubled under locally applied strains. These results highlight the prospect of constructing low-power domain wall gates for magnetic logic devices., The use of electric fields to control the magnetization of ferromagnetic materials could enable more efficient electronics. Lei et al. show that by applying lateral strain to a magnetostrictive nanowire with a piezoelectric, voltage-controlled gating of magnetic domain wall motion in the wire can be achieved.
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- 2013
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8. IL-1β-induced epithelial cell and fibroblast transdifferentiation promotes neutrophil recruitment in chronic rhinosinusitis with nasal polyps.
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Xie X, Wang P, Jin M, Wang Y, Qi L, Wu C, Guo S, Li C, Zhang X, Yuan Y, Ma X, Liu F, Liu W, Liu H, Duan C, Ye P, Li X, Borish L, Zhao W, and Feng X
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- Humans, Animals, Chronic Disease, Mice, Male, Neutrophils metabolism, Neutrophils immunology, Neutrophils drug effects, Female, Disease Models, Animal, Middle Aged, Adult, Rhinosinusitis, Nasal Polyps metabolism, Nasal Polyps pathology, Nasal Polyps immunology, Interleukin-1beta metabolism, Sinusitis metabolism, Sinusitis immunology, Sinusitis pathology, Fibroblasts metabolism, Fibroblasts drug effects, Rhinitis metabolism, Rhinitis pathology, Rhinitis immunology, Neutrophil Infiltration drug effects, Nasal Mucosa pathology, Nasal Mucosa metabolism, Epithelial Cells metabolism, Epithelial Cells drug effects, Cell Transdifferentiation drug effects
- Abstract
Neutrophilic inflammation contributes to multiple chronic inflammatory airway diseases, including asthma and chronic rhinosinusitis with nasal polyps (CRSwNP), and is associated with an unfavorable prognosis. Here, using single-cell RNA sequencing (scRNA-seq) to profile human nasal mucosa obtained from the inferior turbinates, middle turbinates, and nasal polyps of CRSwNP patients, we identify two IL-1 signaling-induced cell subsets-LY6D
+ club cells and IDO1+ fibroblasts-that promote neutrophil recruitment by respectively releasing S100A8/A9 and CXCL1/2/3/5/6/8 into inflammatory regions. IL-1β, a pro-inflammatory cytokine involved in IL-1 signaling, induces the transdifferentiation of LY6D+ club cells and IDO1+ fibroblasts from primary epithelial cells and fibroblasts, respectively. In an LPS-induced neutrophilic CRSwNP mouse model, blocking IL-1β activity with a receptor antagonist significantly reduces the numbers of LY6D+ club cells and IDO1+ fibroblasts and mitigates nasal inflammation. This study implicates the function of two cell subsets in neutrophil recruitment and demonstrates an IL-1-based intervention for mitigating neutrophilic inflammation in CRSwNP., (© 2024. The Author(s).)- Published
- 2024
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9. Asymmetric dihydroboration of allenes enabled by ligand relay catalysis.
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Lei Y, Kong Y, Rong ZQ, and Zhao W
- Abstract
Catalytic asymmetric hydroboration of unsaturated bonds has been recognized as the most straightforward method for the construction of chiral organoboron compounds. Although catalytic asymmetric hydroboration of alkenes has been well-developed, enantioselective hydroboration of allenes still remains rare probably due to the challenges in controlling the enantio-, stereo-, and regioselectivity. Additionally, the hydroboration products might go through over-borohydride, making the catalytic asymmetric dihydroboration of allenes challenging. Here, we report a cobalt-catalyzed asymmetric dihydroboration of allenes using a ligand relay strategy with two simple ligands. This protocol shows excellent enantio-, stereo-, and regioselectivity with positive functional group compatibilities in the construction of chiral 1,4-diboronate products. The applications of this reaction are demonstrated by various product derivatizations, gram-scale reactions, and the preparation of artigenin analogues. Mechanistic studies indicate that the achiral ligand controls the first hydroboration of allenes, and the chiral oxazoline iminopyridine ligand is responsible for the subsequent isomerization and asymmetric hydroboration., (© 2024. The Author(s).)
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- 2024
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10. An expanded database and analytical toolkit for identifying bacterial virulence factors and their associations with chronic diseases.
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Dong W, Fan X, Guo Y, Wang S, Jia S, Lv N, Yuan T, Pan Y, Xue Y, Chen X, Xiong Q, Yang R, Zhao W, and Zhu B
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- Humans, Chronic Disease, Klebsiella pneumoniae genetics, Klebsiella pneumoniae pathogenicity, Klebsiella pneumoniae isolation & purification, Diabetes Mellitus, Type 2 microbiology, Diabetes Mellitus, Type 2 genetics, Escherichia coli genetics, Escherichia coli pathogenicity, Escherichia coli isolation & purification, Bacteria genetics, Bacteria classification, Bacteria isolation & purification, Bacteria pathogenicity, Databases, Genetic, Bacterial Infections microbiology, Virulence Factors genetics, Gastrointestinal Microbiome genetics
- Abstract
Virulence factor genes (VFGs) play pivotal roles in bacterial infections and have been identified within the human gut microbiota. However, their involvement in chronic diseases remains poorly understood. Here, we establish an expanded VFG database (VFDB 2.0) consisting of 62,332 nonredundant orthologues and alleles of VFGs using species-specific average nucleotide identity ( https://github.com/Wanting-Dong/MetaVF_toolkit/tree/main/databases ). We further develop the MetaVF toolkit, facilitating the precise identification of pathobiont-carried VFGs at the species level. A thorough characterization of VFGs for 5452 commensal isolates from healthy individuals reveals that only 11 of 301 species harbour these factors. Further analyses of VFGs within the gut microbiomes of nine chronic diseases reveal both common and disease-specific VFG features. Notably, in type 2 diabetes patients, long HiFi sequencing confirms that shared VF features are carried by pathobiont strains of Escherichia coli and Klebsiella pneumoniae. These findings underscore the critical importance of identifying and understanding VFGs in microbiome-associated diseases., (© 2024. The Author(s).)
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- 2024
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11. Context-aware single-cell multiomics approach identifies cell-type-specific lung cancer susceptibility genes.
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Long E, Yin J, Shin JH, Li Y, Li B, Kane A, Patel H, Sun X, Wang C, Luong T, Xia J, Han Y, Byun J, Zhang T, Zhao W, Landi MT, Rothman N, Lan Q, Chang YS, Yu F, Amos CI, Shi J, Lee JG, Kim EY, and Choi J
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- Humans, Transcriptome, Gene Expression Regulation, Neoplastic, Polymorphism, Single Nucleotide, Chromatin genetics, Chromatin metabolism, Male, Female, Quantitative Trait Loci, Regulatory Sequences, Nucleic Acid genetics, Multiomics, Lung Neoplasms genetics, Lung Neoplasms pathology, Genetic Predisposition to Disease, Genome-Wide Association Study, Single-Cell Analysis methods
- Abstract
Genome-wide association studies (GWAS) identified over fifty loci associated with lung cancer risk. However, underlying mechanisms and target genes are largely unknown, as most risk-associated variants might regulate gene expression in a context-specific manner. Here, we generate a barcode-shared transcriptome and chromatin accessibility map of 117,911 human lung cells from age/sex-matched ever- and never-smokers to profile context-specific gene regulation. Identified candidate cis-regulatory elements (cCREs) are largely cell type-specific, with 37% detected in one cell type. Colocalization of lung cancer candidate causal variants (CCVs) with these cCREs combined with transcription factor footprinting prioritize the variants for 68% of the GWAS loci. CCV-colocalization and trait relevance score indicate that epithelial and immune cell categories, including rare cell types, contribute to lung cancer susceptibility the most. A multi-level cCRE-gene linking system identifies candidate susceptibility genes from 57% of the loci, where most loci display cell-category-specific target genes, suggesting context-specific susceptibility gene function., (© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)
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- 2024
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12. SLC13A3 is a major effector downstream of activated β-catenin in liver cancer pathogenesis.
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Zhao W, Wang X, Han L, Zhang C, Wang C, Kong D, Zhang M, Xu T, Li G, Hu G, Luo J, Yee SW, Yang J, Stahl A, Chen X, and Zhang Y
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- Animals, Humans, Male, Mice, Amino Acid Transport System y+ metabolism, Amino Acid Transport System y+ genetics, Carcinoma, Hepatocellular metabolism, Carcinoma, Hepatocellular genetics, Carcinoma, Hepatocellular pathology, Cell Line, Tumor, Gene Expression Regulation, Neoplastic, Glutathione metabolism, Large Neutral Amino Acid-Transporter 1, Leucine metabolism, Proto-Oncogene Proteins c-myc metabolism, Proto-Oncogene Proteins c-myc genetics, TOR Serine-Threonine Kinases metabolism, Wnt Signaling Pathway, beta Catenin metabolism, beta Catenin genetics, Liver Neoplasms metabolism, Liver Neoplasms genetics, Liver Neoplasms pathology
- Abstract
Activated Wnt/β-catenin pathway is a key genetic event in liver cancer development. Solute carrier (SLC) transporters are promising drug targets. Here, we identify SLC13A3 as a drug-targetable effector downstream of β-catenin in liver cancer. SLC13A3 expression is elevated in human liver cancer samples with gain of function (GOF) mutant CTNNB1, the gene encoding β-catenin. Activation of β-catenin up-regulates SLC13A3, leading to intracellular accumulation of endogenous SLC13A3 substrates. SLC13A3 is identified as a low-affinity transporter for glutathione (GSH). Silencing of SLC13A3 downregulates the leucine transporter SLC7A5 via c-MYC signaling, leading to leucine depletion and mTOR inactivation. Furthermore, silencing of SLC13A3 depletes GSH and induces autophagic ferroptosis in β-catenin-activated liver cancer cells. Importantly, both genetic inhibition of SLC13A3 and a small molecule SLC13A3 inhibitor suppress β-catenin-driven hepatocarcinogenesis in mice. Altogether, our study suggests that SLC13A3 could be a promising therapeutic target for treating human liver cancers with GOF CTNNB1 mutations., (© 2024. The Author(s).)
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- 2024
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13. The proto-oncogene tyrosine kinase c-SRC facilitates glioblastoma progression by remodeling fatty acid synthesis.
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Zhao W, Ouyang C, Zhang L, Wang J, Zhang J, Zhang Y, Huang C, Xiao Q, Jiang B, Lin F, Zhang C, Zhu M, Xie C, Huang X, Zhang B, Zhao W, He J, Chen S, Liu X, Lin D, Li Q, and Wang Z
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- Humans, Cell Line, Tumor, Phosphorylation, Animals, CSK Tyrosine-Protein Kinase metabolism, CSK Tyrosine-Protein Kinase genetics, src-Family Kinases metabolism, src-Family Kinases genetics, Disease Progression, Mice, Brain Neoplasms metabolism, Brain Neoplasms genetics, Brain Neoplasms pathology, NADP metabolism, Mice, Nude, Isocitrate Dehydrogenase genetics, Isocitrate Dehydrogenase metabolism, Glioblastoma metabolism, Glioblastoma genetics, Glioblastoma pathology, Proto-Oncogene Mas, Fatty Acids metabolism, Fatty Acids biosynthesis, Acetyl Coenzyme A metabolism
- Abstract
Increased fatty acid synthesis benefits glioblastoma malignancy. However, the coordinated regulation of cytosolic acetyl-CoA production, the exclusive substrate for fatty acid synthesis, remains unclear. Here, we show that proto-oncogene tyrosine kinase c-SRC is activated in glioblastoma and remodels cytosolic acetyl-CoA production for fatty acid synthesis. Firstly, acetate is an important substrate for fatty acid synthesis in glioblastoma. c-SRC phosphorylates acetyl-CoA synthetase ACSS2 at Tyr530 and Tyr562 to stimulate the conversion of acetate to acetyl-CoA in cytosol. Secondly, c-SRC inhibits citrate-derived acetyl-CoA synthesis by phosphorylating ATP-citrate lyase ACLY at Tyr682. ACLY phosphorylation shunts citrate to IDH1-catalyzed NADPH production to provide reducing equivalent for fatty acid synthesis. The c-SRC-unresponsive double-mutation of ACSS2 and ACLY significantly reduces fatty acid synthesis and hampers glioblastoma progression. In conclusion, this remodeling fulfills the dual needs of glioblastoma cells for both acetyl-CoA and NADPH in fatty acid synthesis and provides evidence for glioma treatment by c-SRC inhibition., (© 2024. The Author(s).)
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- 2024
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14. Publisher Correction: Kagomerization of transition metal monolayers induced by two-dimensional hexagonal boron nitride.
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Zhou H, Dos Santos Dias M, Zhang Y, Zhao W, and Lounis S
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- 2024
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15. Generation of out-of-plane polarized spin current by non-uniform oxygen octahedral tilt/rotation.
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Han F, Zhang J, Yang F, Li B, He Y, Li G, Chen Y, Jiang Q, Huang Y, Zhang H, Zhang J, Yang H, Liu H, Zhang Q, Wu H, Chen J, Zhao W, Sheng XL, Sun J, and Zhang Y
- Abstract
The free-field switching of the perpendicular magnetization by the out-of-plane polarized spin current induced spin-orbit torque makes it a promising technology for developing high-density memory and logic devices. The materials intrinsically with low symmetry are generally utilized to generate the spin current with out-of-plane spin polarization. However, the generation of the out-of-plane polarized spin current by engineering the symmetry of materials has not yet been reported. Here, we demonstrate that paramagnetic CaRuO
3 films are able to generate out-of-plane polarized spin current by engineering the crystal symmetry. The non-uniform oxygen octahedral tilt/rotation along film's normal direction induced by oxygen octahedral coupling near interface breaks the screw-axis and glide-plane symmetries, which gives rise to a significant out-of-plane polarized spin current. This spin current can drive field-free spin-orbit torque switching of perpendicular magnetization with high efficiency. Our results offer a promising strategy based on crystal symmetry design to manipulate spin current and could have potential applications in advanced spintronic devices., (© 2024. The Author(s).)- Published
- 2024
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16. DSS1 restrains BRCA2's engagement with dsDNA for homologous recombination, replication fork protection, and R-loop homeostasis.
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Huang Y, Li W, Foo T, Ji JH, Wu B, Tomimatsu N, Fang Q, Gao B, Long M, Xu J, Maqbool R, Mukherjee B, Ni T, Alejo S, He Y, Burma S, Lan L, Xia B, and Zhao W
- Subjects
- Humans, Homeostasis, Protein Binding, DNA-Binding Proteins metabolism, DNA-Binding Proteins genetics, Protein Domains, Cell Line, Tumor, DNA Damage, Proteasome Endopeptidase Complex, BRCA2 Protein metabolism, BRCA2 Protein genetics, BRCA2 Protein chemistry, DNA Replication, Homologous Recombination, DNA metabolism, Rad51 Recombinase metabolism, Rad51 Recombinase genetics, Mutation, DNA, Single-Stranded metabolism, DNA, Single-Stranded genetics
- Abstract
DSS1, essential for BRCA2-RAD51 dependent homologous recombination (HR), associates with the helical domain (HD) and OB fold 1 (OB1) of the BRCA2 DSS1/DNA-binding domain (DBD) which is frequently targeted by cancer-associated pathogenic variants. Herein, we reveal robust ss/dsDNA binding abilities in HD-OB1 subdomains and find that DSS1 shuts down HD-OB1's DNA binding to enable ssDNA targeting of the BRCA2-RAD51 complex. We show that C-terminal helix mutations of DSS1, including the cancer-associated R57Q mutation, disrupt this DSS1 regulation and permit dsDNA binding of HD-OB1/BRCA2-DBD. Importantly, these DSS1 mutations impair BRCA2/RAD51 ssDNA loading and focus formation and cause decreased HR efficiency, destabilization of stalled forks and R-loop accumulation, and hypersensitize cells to DNA-damaging agents. We propose that DSS1 restrains the intrinsic dsDNA binding of BRCA2-DBD to ensure BRCA2/RAD51 targeting to ssDNA, thereby promoting optimal execution of HR, and potentially replication fork protection and R-loop suppression., (© 2024. The Author(s).)
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- 2024
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17. Nanoscale covalent organic frameworks for enhanced photocatalytic hydrogen production.
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Zhao W, Luo L, Cong M, Liu X, Zhang Z, Bahri M, Li B, Yang J, Yu M, Liu L, Xia Y, Browning ND, Zhu WH, Zhang W, and Cooper AI
- Abstract
Nanosizing confers unique functions in materials such as graphene and quantum dots. Here, we present two nanoscale-covalent organic frameworks (nano-COFs) that exhibit exceptionally high activity for photocatalytic hydrogen production that results from their size and morphology. Compared to bulk analogues, the downsizing of COFs crystals using surfactants provides greatly improved water dispersibility and light-harvesting properties. One of these nano-COFs shows a hydrogen evolution rate of 392.0 mmol g
-1 h-1 (33.3 μmol h-1 ), which is one of the highest mass-normalized rates reported for a COF or any other organic photocatalysts. A reverse concentration-dependent photocatalytic phenomenon is observed, whereby a higher photocatalytic activity is found at a lower catalyst concentration. These materials also show a molecule-like excitonic nature, as studied by photoluminescence and transient absorption spectroscopy, which is again a function of their nanoscale dimensions. This charts a new path to highly efficient organic photocatalysts for solar fuel production., (© 2024. The Author(s).)- Published
- 2024
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18. Delocalized electronic engineering of TiNb 2 O 7 enables low temperature capability for high-areal-capacity lithium-ion batteries.
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Zhang Y, Wang Y, Zhao W, Zuo P, Tong Y, Yin G, Zhu T, and Lou S
- Abstract
High areal capacity and low-temperature ability are critical for lithium-ion batteries (LIBs). However, the practical operation is seriously impeded by the sluggish rates of mass and charge transfer. Herein, the active electronic states of TiNb
2 O7 material is modulated by dopant and O-vacancies for enhanced low-temperature dynamics. Femtosecond laser-based transient absorption spectroscopy is employed to depict carrier dynamics of TiNb2 O7 , which verifies the localized structure polarization accounting for reduced transport overpotential, facilitated electron/ion transport, and improved Li+ adsorption. At high-mass loading of 10 mg cm-2 and -30 °C, TNO-x @N microflowers exhibit stable cycling performance with 92.9% capacity retention over 250 cycles at 1 C (1.0-3.0 V, 1 C = 250 mA g-1 ). Even at -40 °C, a competitive areal capacity of 1.32 mAh cm-2 can be achieved. Such a fundamental understanding of the intrinsic structure-function put forward a rational viewpoint for designing high-areal-capacity batteries in cold regions., (© 2024. The Author(s).)- Published
- 2024
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19. Efficacy of the tetravalent protein COVID-19 vaccine, SCTV01E: a phase 3 double-blind, randomized, placebo-controlled trial.
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Zhang R, Zhao J, Zhu X, Guan Q, Liu S, Li M, Gao J, Tan J, Cao F, Gan B, Wu B, Bai J, Liu Y, Xie G, Liu C, Zhao W, Yan L, Xu S, Qian G, Liu D, Li J, Li W, Tian X, Wang J, Wang S, Li D, Li J, Jiao Y, Li X, Chen Y, Wang Y, Gai W, Zhou Q, and Xie L
- Subjects
- Humans, Double-Blind Method, Female, Male, Adult, Middle Aged, Spike Glycoprotein, Coronavirus immunology, Antibodies, Neutralizing immunology, Aged, Young Adult, Immunogenicity, Vaccine, Adolescent, Vaccination methods, COVID-19 Vaccines immunology, COVID-19 Vaccines administration & dosage, COVID-19 Vaccines adverse effects, COVID-19 prevention & control, COVID-19 immunology, COVID-19 virology, SARS-CoV-2 immunology, Antibodies, Viral immunology, Vaccine Efficacy
- Abstract
Evolution of SARS-CoV-2 variants emphasizes the need for multivalent vaccines capable of simultaneously targeting multiple strains. SCTV01E is a tetravalent COVID-19 vaccine derived from the spike protein of SARS-CoV-2 variants Alpha, Beta, Delta, and Omicron BA.1. In this double-blinded placebo-controlled pivotal efficacy trial (NCT05308576), the primary endpoint was vaccine efficacy (VE) against COVID-19 seven days post-vaccination in individuals without recent infection. Other endpoints included evaluating safety, immunogenicity, and the VE against all SARS-CoV-2 infections in individuals meeting the study criteria. Between December 26, 2022, and January 15, 2023, 9,223 individuals were randomized at a 1:1 ratio to receive SCTV01E or a placebo. SCTV01E showed a VE of 69.4% (95% CI: 50.6, 81.0) 7 days post-vaccination, with 75 cases in the placebo group and 23 in the SCTV01E group for the primary endpoint. VEs were 79.7% (95% CI: 51.0, 91.6) and 82.4% (95% CI: 57.9, 92.6), respectively, for preventing symptomatic infection and all SARS-CoV-2 infections 14 days post-vaccination. SCTV01E elicited a 25.0-fold higher neutralizing antibody response against Omicron BA.5 28 days post-vaccination compared to placebo. Reactogenicity was generally mild and transient, with no reported vaccine-related SAE, adverse events of special interest (AESI), or deaths. The trial aligned with the shift from dominant variants BA.5 and BF.7 to XBB, suggesting SCTV01E as a potential vaccine alternative effective against present and future variants., (© 2024. The Author(s).)
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- 2024
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20. Thermo-adaptive interfacial solar evaporation enhanced by dynamic water gating.
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Wang Y, Zhao W, Lee Y, Li Y, Wang Z, and Tam KC
- Abstract
Solar-driven evaporation offers a sustainable solution for water purification, but efficiency losses due to heat dissipation and fouling limit its scalability. Herein, we present a bilayer-structured solar evaporator (SDWE) with dynamic fluidic flow mechanism, designed to ensure a thin water supply and self-cleaning capability. The porous polydopamine (PDA) layer on a nickel skeleton provides photothermal functionality and water microchannels, while the thermo-responsive sporopollenin layer on the bottom acts as a switchable water gate. Using confocal laser microscopy and micro-CT, we demonstrate that this unique structure ensures a steady supply of thin water layers, enhancing evaporation by minimizing latent heat at high temperatures. Additionally, the system initiates a self-cleaning process through bulk water convection when temperature drops due to salt accumulation, thus maintaining increased evaporation efficiency. Therefore, the optimized p-SDWE sample achieved a high evaporation rate of 3.58 kg m
-2 h-1 using 93.9% solar energy from 1 sun irradiation, and produces 18-22 liters of purified water per square meter of SDWE per day from brine water. This dynamic water transport mechanism surpasses traditional day-night cycles, offering inherent thermal adaptability for continuous, high-efficiency evaporation., (© 2024. The Author(s).)- Published
- 2024
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21. Flexible tungsten disulfide superstructure engineering for efficient alkaline hydrogen evolution in anion exchange membrane water electrolysers.
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Xie L, Wang L, Liu X, Chen J, Wen X, Zhao W, Liu S, and Zhao Q
- Abstract
Anion exchange membrane (AEM) water electrolysis employing non-precious metal electrocatalysts is a promising strategy for achieving sustainable hydrogen production. However, it still suffers from many challenges, including sluggish alkaline hydrogen evolution reaction (HER) kinetics, insufficient activity and limited lifetime of non-precious metal electrocatalysts for ampere-level-current-density alkaline HER. Here, we report an efficient alkaline HER strategy at industrial-level current density wherein a flexible WS
2 superstructure is designed to serve as the cathode catalyst for AEM water electrolysis. The superstructure features bond-free van der Waals interaction among the low Young's modulus nanosheets to ensure excellent mechanical flexibility, as well as a stepped edge defect structure of nanosheets to realize high catalytic activity and a favorable reaction interface micro-environment. The unique flexible WS2 superstructure can effectively withstand the impact of high-density gas-liquid exchanges and facilitate mass transfer, endowing excellent long-term durability under industrial-scale current density. An AEM electrolyser containing this catalyst at the cathode exhibits a cell voltage of 1.70 V to deliver a constant catalytic current density of 1 A cm-2 over 1000 h with a negligible decay rate of 9.67 μV h-1 ., (© 2024. The Author(s).)- Published
- 2024
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22. CRISPR screens reveal convergent targeting strategies against evolutionarily distinct chemoresistance in cancer.
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Zhong C, Jiang WJ, Yao Y, Li Z, Li Y, Wang S, Wang X, Zhu W, Wu S, Wang J, Fan S, Ma S, Liu Y, Zhang H, Zhao W, Zhao L, Feng Y, Li Z, Guo R, Yu L, Pei F, Hu J, Feng X, Yang Z, Yang Z, Yang X, Hou Y, Zhang D, Xu D, Sheng R, Li Y, Liu L, Wu HJ, Huang J, and Fei T
- Subjects
- Humans, Cell Line, Tumor, Colorectal Neoplasms genetics, Colorectal Neoplasms drug therapy, Animals, Neoplasms genetics, Neoplasms drug therapy, Clustered Regularly Interspaced Short Palindromic Repeats genetics, Mice, Gene Expression Regulation, Neoplastic drug effects, Drug Resistance, Neoplasm genetics, Antineoplastic Agents pharmacology, Antineoplastic Agents therapeutic use, Oxaliplatin pharmacology, Irinotecan pharmacology, CRISPR-Cas Systems genetics, Protein Serine-Threonine Kinases genetics, Protein Serine-Threonine Kinases metabolism, Protein Serine-Threonine Kinases antagonists & inhibitors
- Abstract
Resistance to chemotherapy has been a major hurdle that limits therapeutic benefits for many types of cancer. Here we systematically identify genetic drivers underlying chemoresistance by performing 30 genome-scale CRISPR knockout screens for seven chemotherapeutic agents in multiple cancer cells. Chemoresistance genes vary between conditions primarily due to distinct genetic background and mechanism of action of drugs, manifesting heterogeneous and multiplexed routes towards chemoresistance. By focusing on oxaliplatin and irinotecan resistance in colorectal cancer, we unravel that evolutionarily distinct chemoresistance can share consensus vulnerabilities identified by 26 second-round CRISPR screens with druggable gene library. We further pinpoint PLK4 as a therapeutic target to overcome oxaliplatin resistance in various models via genetic ablation or pharmacological inhibition, highlighting a single-agent strategy to antagonize evolutionarily distinct chemoresistance. Our study not only provides resources and insights into the molecular basis of chemoresistance, but also proposes potential biomarkers and therapeutic strategies against such resistance., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
23. Kagomerization of transition metal monolayers induced by two-dimensional hexagonal boron nitride.
- Author
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Zhou H, Dos Santos Dias M, Zhang Y, Zhao W, and Lounis S
- Abstract
The kagome lattice is an exciting solid state physics platform for the emergence of nontrivial quantum states driven by electronic correlations: topological effects, unconventional superconductivity, charge and spin density waves, and unusual magnetic states such as quantum spin liquids. While kagome lattices have been realized in complex multi-atomic bulk compounds, here we demonstrate from first-principles a process that we dub kagomerization, in which we fabricate a two-dimensional kagome lattice in monolayers of transition metals utilizing an hexagonal boron nitride (h-BN) overlayer. Surprisingly, h-BN induces a large rearrangement of the transition metal atoms supported on a fcc(111) heavy-metal surface. This reconstruction is found to be rather generic for this type of heterostructures and has a profound impact on the underlying magnetic properties, ultimately stabilizing various topological magnetic solitons such as skyrmions and bimerons. Our findings call for a reconsideration of h-BN as merely a passive capping layer, showing its potential for not only reconstructing the atomic structure of the underlying material, e.g. through the kagomerization of magnetic films, but also enabling electronic and magnetic phases that are highly sought for the next generation of device technologies., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
24. Evolved histone tail regulates 53BP1 recruitment at damaged chromatin.
- Author
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Kelliher JL, Folkerts ML, Shen KV, Song W, Tengler K, Stiefel CM, Lee SO, Dray E, Zhao W, Koss B, Pannunzio NR, and Leung JW
- Subjects
- Humans, Adaptor Proteins, Signal Transducing, BRCA1 Protein metabolism, BRCA1 Protein genetics, Camptothecin pharmacology, Cell Cycle Proteins, DNA Repair, HEK293 Cells, Phosphorylation, Ubiquitin-Protein Ligases metabolism, Ubiquitin-Protein Ligases genetics, Chromatin metabolism, DNA Damage, Histones metabolism, Histones genetics, Tumor Suppressor p53-Binding Protein 1 metabolism, Tumor Suppressor p53-Binding Protein 1 genetics, Ubiquitination
- Abstract
The master DNA damage repair histone protein, H2AX, is essential for orchestrating the recruitment of downstream mediator and effector proteins at damaged chromatin. The phosphorylation of H2AX at S139, γH2AX, is well-studied for its DNA repair function. However, the extended C-terminal tail is not characterized. Here, we define the minimal motif on H2AX for the canonical function in activating the MDC1-RNF8-RNF168 phosphorylation-ubiquitination pathway that is important for recruiting repair proteins, such as 53BP1 and BRCA1. Interestingly, H2AX recruits 53BP1 independently from the MDC1-RNF8-RNF168 pathway through its evolved C-terminal linker region with S139 phosphorylation. Mechanistically, 53BP1 recruitment to damaged chromatin is mediated by the interaction between the H2AX C-terminal tail and the 53BP1 Oligomerization-Tudor domains. Moreover, γH2AX-linker mediated 53BP1 recruitment leads to camptothecin resistance in H2AX knockout cells. Overall, our study uncovers an evolved mechanism within the H2AX C-terminal tail for regulating DNA repair proteins at damaged chromatin., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
25. A fully autonomous robotic ultrasound system for thyroid scanning.
- Author
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Su K, Liu J, Ren X, Huo Y, Du G, Zhao W, Wang X, Liang B, Li D, and Liu PX
- Subjects
- Humans, Bayes Theorem, Female, Adult, Male, Thyroid Neoplasms diagnostic imaging, Thyroid Gland diagnostic imaging, Ultrasonography methods, Ultrasonography instrumentation, Robotics methods, Robotics instrumentation, Thyroid Nodule diagnostic imaging, Thyroid Nodule pathology
- Abstract
The current thyroid ultrasound relies heavily on the experience and skills of the sonographer and the expertise of the radiologist, and the process is physically and cognitively exhausting. In this paper, we report a fully autonomous robotic ultrasound system, which is able to scan thyroid regions without human assistance and identify malignant nod- ules. In this system, human skeleton point recognition, reinforcement learning, and force feedback are used to deal with the difficulties in locating thyroid targets. The orientation of the ultrasound probe is adjusted dynamically via Bayesian optimization. Experimental results on human participants demonstrated that this system can perform high-quality ultrasound scans, close to manual scans obtained by clinicians. Additionally, it has the potential to detect thyroid nodules and provide data on nodule characteristics for American College of Radiology Thyroid Imaging Reporting and Data System (ACR TI-RADS) calculation., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
26. Ocean internal tides suppress tropical cyclones in the South China Sea.
- Author
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Guan S, Jin FF, Tian J, Lin II, Pun IF, Zhao W, Huthnance J, Xu Z, Cai W, Jing Z, Zhou L, Liu P, Zhang Y, Zhang Z, Zhou C, Yang Q, Huang X, Hou Y, and Song J
- Abstract
Tropical Cyclones (TCs) are devastating natural disasters. Analyzing four decades of global TC data, here we find that among all global TC-active basins, the South China Sea (SCS) stands out as particularly difficult ocean for TCs to intensify, despite favorable atmosphere and ocean conditions. Over the SCS, TC intensification rate and its probability for a rapid intensification (intensification by ≥ 15.4 m s
-1 day-1 ) are only 1/2 and 1/3, respectively, of those for the rest of the world ocean. Originating from complex interplays between astronomic tides and the SCS topography, gigantic ocean internal tides interact with TC-generated oceanic near-inertial waves and induce a strong ocean cooling effect, suppressing the TC intensification. Inclusion of this interaction between internal tides and TC in operational weather prediction systems is expected to improve forecast of TC intensity in the SCS and in other regions where strong internal tides are present., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
27. General strategy for developing thick-film micro-thermoelectric coolers from material fabrication to device integration.
- Author
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Sun X, Yan Y, Kang M, Zhao W, Yan K, Wang H, Li R, Zhao S, Hua X, Wang B, Zhang W, and Deng Y
- Abstract
Micro-thermoelectric coolers are emerging as a promising solution for high-density cooling applications in confined spaces. Unlike thin-film micro-thermoelectric coolers with high cooling flux at the expense of cooling temperature difference due to very short thermoelectric legs, thick-film micro-thermoelectric coolers can achieve better comprehensive cooling performance. However, they still face significant challenges in both material preparation and device integration. Herein, we propose a design strategy which combines Bi
2 Te3 -based thick film prepared by powder direct molding with micro-thermoelectric cooler integrated via phase-change batch transfer. Accurate thickness control and relatively high thermoelectric performance can be achieved for the thick film, and the high-density-integrated thick-film micro-thermoelectric cooler exhibits excellent performance with maximum cooling temperature difference of 40.6 K and maximum cooling flux of 56.5 W·cm-2 at room temperature. The micro-thermoelectric cooler also shows high temperature control accuracy (0.01 K) and reliability (over 30000 cooling cycles). Moreover, the device demonstrates remarkable capacity in power generation with normalized power density up to 214.0 μW · cm-2 · K-2 . This study provides a general and scalable route for developing high-performance thick-film micro-thermoelectric cooler, benefiting widespread applications in thermal management of microsystems., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
28. Universal scaling law for chiral antiferromagnetism.
- Author
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Xu S, Dai B, Jiang Y, Xiong D, Cheng H, Tai L, Tang M, Sun Y, He Y, Yang B, Peng Y, Wang KL, and Zhao W
- Abstract
The chiral antiferromagnetic (AFM) materials, which have been widely investigated due to their rich physics, such as non-zero Berry phase and topology, provide a platform for the development of antiferromagnetic spintronics. Here, we find two distinctive anomalous Hall effect (AHE) contributions in the chiral AFM Mn
3 Pt, originating from a time-reversal symmetry breaking induced intrinsic mechanism and a skew scattering induced topological AHE due to an out-of-plane spin canting with respect to the Kagome plane. We propose a universal AHE scaling law to explain the AHE resistivity ( ρ A H ) in this chiral magnet, with both a scalar spin chirality (SSC)-induced skew scattering topological AHE term, a s k and non-collinear spin-texture induced intrinsic anomalous Hall term, b i n . We found that a s k and b i n can be effectively modulated by the interfacial electron scattering, exhibiting a linear relation with the inverse film thickness. Moreover, the scaling law can explain the anomalous Hall effect in various chiral magnets and has far-reaching implications for chiral-based spintronics devices., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
29. Enabling robust blue circularly polarized organic afterglow through self-confining isolated chiral chromophore.
- Author
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Zeng M, Wang W, Zhang S, Gao Z, Yan Y, Liu Y, Qi Y, Yan X, Zhao W, Zhang X, Guo N, Li H, Li H, Xie G, Tao Y, Chen R, and Huang W
- Abstract
Creating circularly polarized organic afterglow system with elevated triplet energy levels, suppressed non-radiative transitions, and effective chirality, which are three critical prerequisites for achieving blue circularly polarized afterglow, has posed a formidable challenge. Herein, a straightforward approach is unveiled to attain blue circularly polarized afterglow materials by covalently self-confining isolated chiral chromophore within polymer matrix. The formation of robust hydrogen bonds within the polymer matrix confers a distinctly isolated and stabilized molecular state of chiral chromophores, endowing a blue emission band at 414 nm, lifetime of 3.0 s, and luminescent dissymmetry factor of ~ 10
-2 . Utilizing the synergistic afterglow and chirality energy transfer, full-color circularly polarized afterglow systems are endowed by doping colorful fluorescent molecules into designed blue polymers, empowering versatile applications. This work paves the way for the streamlined design of blue circularly polarized afterglow materials, expanding the horizons of circularly polarized afterglow materials into various domains., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
30. Universal inter-molecular radical transfer reactions on metal surfaces.
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Wang J, Niu K, Zhu H, Xu C, Deng C, Zhao W, Huang P, Lin H, Li D, Rosen J, Liu P, Allegretti F, Barth JV, Yang B, Björk J, Li Q, and Chi L
- Abstract
On-surface synthesis provides tools to prepare low-dimensional supramolecular structures. Traditionally, reactive radicals are a class of single-electron species, serving as exceptional electron-withdrawing groups. On metal surfaces, however, such species are affected by conduction band screening effects that may even quench their unpaired electron characteristics. As a result, radicals are expected to be less active, and reactions catalyzed by surface-stabilized radicals are rarely reported. Herein, we describe a class of inter-molecular radical transfer reactions on metal surfaces. With the assistance of aryl halide precursors, the coupling of terminal alkynes is steered from non-dehydrogenated to dehydrogenated products, resulting in alkynyl-Ag-alkynyl bonds. Dehalogenated molecules are fully passivated by detached hydrogen atoms. The reaction mechanism is unraveled by various surface-sensitive technologies and density functional theory calculations. Moreover, we reveal the universality of this mechanism on metal surfaces. Our studies enrich the on-surface synthesis toolbox and develop a pathway for producing low-dimensional organic materials., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
31. High-security learning-based optical encryption assisted by disordered metasurface.
- Author
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Yu Z, Li H, Zhao W, Huang PS, Lin YT, Yao J, Li W, Zhao Q, Wu PC, Li B, Genevet P, Song Q, and Lai P
- Abstract
Artificial intelligence has gained significant attention for exploiting optical scattering for optical encryption. Conventional scattering media are inevitably influenced by instability or perturbations, and hence unsuitable for long-term scenarios. Additionally, the plaintext can be easily compromised due to the single channel within the medium and one-to-one mapping between input and output. To mitigate these issues, a stable spin-multiplexing disordered metasurface (DM) with numerous polarized transmission channels serves as the scattering medium, and a double-secure procedure with superposition of plaintext and security key achieves two-to-one mapping between input and output. In attack analysis, when the ciphertext, security key, and incident polarization are all correct, the plaintext can be decrypted. This system demonstrates excellent decryption efficiency over extended periods in noisy environments. The DM, functioning as an ultra-stable and active speckle generator, coupled with the double-secure approach, creates a highly secure speckle-based cryptosystem with immense potentials for practical applications., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
32. Asymmetric synthesis of P-stereogenic phosphindane oxides via kinetic resolution and their biological activity.
- Author
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Yin L, Li J, Wu C, Zhang H, Zhao W, Fan Z, Liu M, Zhang S, Guo M, Dou X, and Guo D
- Subjects
- Humans, Catalysis, Drug Discovery, Kinetics, Oxides pharmacology, Polycystic Kidney, Autosomal Dominant
- Abstract
The importance of P-stereogenic heterocycles has been widely recognized with their extensive use as privileged chiral ligands and bioactive compounds. The catalytic asymmetric synthesis of P-stereogenic phosphindane derivatives, however, remains a challenging task. Herein, we report a catalytic kinetic resolution of phosphindole oxides via rhodium-catalyzed diastereo- and enantioselective conjugate addition to access enantiopure P-stereogenic phosphindane and phosphindole derivatives. This kinetic resolution method features high efficiency (s factor up to >1057), excellent stereoselectivities (all >20:1 dr, up to >99% ee), and a broad substrate scope. The obtained chiral phosphindane oxides exhibit promising therapeutic efficacy in autosomal dominant polycystic kidney disease (ADPKD), and compound 3az is found to significantly inhibit renal cyst growth both in vitro and in vivo, thus ushering in a promising scaffold for ADPKD drug discovery. This study will not only advance efforts towards the asymmetric synthesis of challenging P-stereogenic heterocycles, but also surely inspire further development of P-stereogenic entities for bioactive small-molecule discovery., (© 2024. The Author(s).)
- Published
- 2024
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- View/download PDF
33. Elevation-dependent pattern of net CO 2 uptake across China.
- Author
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Wei D, Tao J, Wang Z, Zhao H, Zhao W, and Wang X
- Subjects
- Temperature, Hot Temperature, China, Ecosystem, Carbon Dioxide
- Abstract
The elevation gradient has long been known to be vital in shaping the structure and function of terrestrial ecosystems, but little is known about the elevation-dependent pattern of net CO
2 uptake, denoted by net ecosystem productivity (NEP). Here, by analyzing data from 203 eddy covariance sites across China, we report a negative linear elevation-dependent pattern of NEP, collectively shaped by varying hydrothermal factors, nutrient supply, and ecosystem types. Furthermore, the NEP shows a higher temperature sensitivity in high-elevation environments (3000-5000 m) compared with the lower-elevation environments (<3000 m). Model ensemble and satellite-based observations consistently reveal more rapid relative changes in NEP in high-elevation environments during the last four decades. Machine learning also predicts a stronger relative increase in high-elevation environments, whereas less change is expected at lower elevations. We therefore conclude a varying elevation-dependent pattern of the NEP of terrestrial ecosystems in China, although there is significant uncertainty involved., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
34. Epigenetic profiling reveals key genes and cis-regulatory networks specific to human parathyroids.
- Author
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Jung YL, Zhao W, Li I, Jain D, Epstein CB, Bernstein BE, Parangi S, Sherwood R, Robinson-Cohen C, Hsu YH, Park PJ, and Mannstadt M
- Subjects
- Animals, Humans, Parathyroid Hormone genetics, Parathyroid Hormone metabolism, Chromatin genetics, Epigenesis, Genetic, Calcium metabolism, Parathyroid Glands metabolism
- Abstract
In all terrestrial vertebrates, the parathyroid glands are critical regulators of calcium homeostasis and the sole source of parathyroid hormone (PTH). Hyperparathyroidism and hypoparathyroidism are clinically important disorders affecting multiple organs. However, our knowledge regarding regulatory mechanisms governing the parathyroids has remained limited. Here, we present the comprehensive maps of the chromatin landscape of the human parathyroid glands, identifying active regulatory elements and chromatin interactions. These data allow us to define regulatory circuits and previously unidentified genes that play crucial roles in parathyroid biology. We experimentally validate candidate parathyroid-specific enhancers and demonstrate their integration with GWAS SNPs for parathyroid-related diseases and traits. For instance, we observe reduced activity of a parathyroid-specific enhancer of the Calcium Sensing Receptor gene, which contains a risk allele associated with higher PTH levels compared to the wildtype allele. Our datasets provide a valuable resource for unraveling the mechanisms governing parathyroid gland regulation in health and disease., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
35. Orbitronics: light-induced orbital currents in Ni studied by terahertz emission experiments.
- Author
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Xu Y, Zhang F, Fert A, Jaffres HY, Liu Y, Xu R, Jiang Y, Cheng H, and Zhao W
- Abstract
Orbitronics is based on the use of orbital currents as information carriers. Orbital currents can be generated from the conversion of charge or spin currents, and inversely, they could be converted back to charge or spin currents. Here we demonstrate that orbital currents can also be generated by femtosecond light pulses on Ni. In multilayers associating Ni with oxides and nonmagnetic metals such as Cu, we detect the orbital currents by their conversion into charge currents and the resulting terahertz emission. We show that the orbital currents extraordinarily predominate the light-induced spin currents in Ni-based systems, whereas only spin currents can be detected with CoFeB-based systems. In addition, the analysis of the time delays of the terahertz pulses leads to relevant information on the velocity and propagation length of orbital carriers. Our finding of light-induced orbital currents and our observation of their conversion into charge currents opens new avenues in orbitronics, including the development of orbitronic terahertz devices., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
36. BTLA contributes to acute-on-chronic liver failure infection and mortality through CD4 + T-cell exhaustion.
- Author
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Yu X, Yang F, Shen Z, Zhang Y, Sun J, Qiu C, Zheng Y, Zhao W, Yuan S, Zeng D, Zhang S, Long J, Zhu M, Zhang X, Wu J, Ma Z, Zhu H, Su M, Xu J, Li B, Mao R, Su Z, and Zhang J
- Subjects
- Animals, Humans, Mice, CD4-Positive T-Lymphocytes, Cytokines metabolism, Phosphatidylinositol 3-Kinases, Receptors, Immunologic metabolism, T-Cell Exhaustion, Acute-On-Chronic Liver Failure complications, Hepatitis B, Chronic complications
- Abstract
B- and T-lymphocyte attenuator (BTLA) levels are increased in patients with hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF). This condition is characterized by susceptibility to infection and T-cell immune exhaustion. However, whether BTLA can induce T-cell immune exhaustion and increase the risk of infection remains unclear. Here, we report that BTLA levels are significantly increased in the circulating and intrahepatic CD4
+ T cells from patients with HBV-ACLF, and are positively correlated with disease severity, prognosis, and infection complications. BTLA levels were upregulated by the IL-6 and TNF signaling pathways. Antibody crosslinking of BTLA activated the PI3K-Akt pathway to inhibit the activation, proliferation, and cytokine production of CD4+ T cells while promoting their apoptosis. In contrast, BTLA knockdown promoted their activation and proliferation. BTLA-/- ACLF mice exhibited increased cytokine secretion, and reduced mortality and bacterial burden. The administration of a neutralizing anti-BTLA antibody reduced Klebsiella pneumoniae load and mortality in mice with ACLF. These data may help elucidate HBV-ACLF pathogenesis and aid in identifying novel drug targets., (© 2024. The Author(s).)- Published
- 2024
- Full Text
- View/download PDF
37. S-nitrosothiol homeostasis maintained by ADH5 facilitates STING-dependent host defense against pathogens.
- Author
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Jia M, Chai L, Wang J, Wang M, Qin D, Song H, Fu Y, Zhao C, Gao C, Jia J, and Zhao W
- Subjects
- Membrane Proteins metabolism, Immunity, Innate, Homeostasis, S-Nitrosothiols, Herpesvirus 1, Human, Aldehyde Oxidoreductases
- Abstract
Oxidative (or respiratory) burst confers host defense against pathogens by generating reactive species, including reactive nitrogen species (RNS). The microbial infection-induced excessive RNS damages many biological molecules via S-nitrosothiol (SNO) accumulation. However, the mechanism by which the host enables innate immunity activation during oxidative burst remains largely unknown. Here, we demonstrate that S-nitrosoglutathione (GSNO), the main endogenous SNO, attenuates innate immune responses against herpes simplex virus-1 (HSV-1) and Listeria monocytogenes infections. Mechanistically, GSNO induces the S-nitrosylation of stimulator of interferon genes (STING) at Cys257, inhibiting its binding to the second messenger cyclic guanosine monophosphate-adenosine monophosphate (cGAMP). Alcohol dehydrogenase 5 (ADH5), the key enzyme that metabolizes GSNO to decrease cellular SNOs, facilitates STING activation by inhibiting S-nitrosylation. Concordantly, Adh5 deficiency show defective STING-dependent immune responses upon microbial challenge and facilitates viral replication. Thus, cellular oxidative burst-induced RNS attenuates the STING-mediated innate immune responses to microbial infection, while ADH5 licenses STING activation by maintaining cellular SNO homeostasis., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
38. Tunable positions of Weyl nodes via magnetism and pressure in the ferromagnetic Weyl semimetal CeAlSi.
- Author
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Cheng E, Yan L, Shi X, Lou R, Fedorov A, Behnami M, Yuan J, Yang P, Wang B, Cheng JG, Xu Y, Xu Y, Xia W, Pavlovskii N, Peets DC, Zhao W, Wan Y, Burkhardt U, Guo Y, Li S, Felser C, Yang W, and Büchner B
- Abstract
The noncentrosymmetric ferromagnetic Weyl semimetal CeAlSi with simultaneous space-inversion and time-reversal symmetry breaking provides a unique platform for exploring novel topological states. Here, by employing multiple experimental techniques, we demonstrate that ferromagnetism and pressure can serve as efficient parameters to tune the positions of Weyl nodes in CeAlSi. At ambient pressure, a magnetism-facilitated anomalous Hall/Nernst effect (AHE/ANE) is uncovered. Angle-resolved photoemission spectroscopy (ARPES) measurements demonstrated that the Weyl nodes with opposite chirality are moving away from each other upon entering the ferromagnetic phase. Under pressure, by tracing the pressure evolution of AHE and band structure, we demonstrate that pressure could also serve as a pivotal knob to tune the positions of Weyl nodes. Moreover, multiple pressure-induced phase transitions are also revealed. These findings indicate that CeAlSi provides a unique and tunable platform for exploring exotic topological physics and electron correlations, as well as catering to potential applications, such as spintronics., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
39. Phase-engineered synthesis of atomically thin te single crystals with high on-state currents.
- Author
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Zhou J, Zhang G, Wang W, Chen Q, Zhao W, Liu H, Zhao B, Ni Z, and Lu J
- Abstract
Multiple structural phases of tellurium (Te) have opened up various opportunities for the development of two-dimensional (2D) electronics and optoelectronics. However, the phase-engineered synthesis of 2D Te at the atomic level remains a substantial challenge. Herein, we design an atomic cluster density and interface-guided multiple control strategy for phase- and thickness-controlled synthesis of α-Te nanosheets and β-Te nanoribbons (from monolayer to tens of μm) on WS
2 substrates. As the thickness decreases, the α-Te nanosheets exhibit a transition from metallic to n-type semiconducting properties. On the other hand, the β-Te nanoribbons remain p-type semiconductors with an ON-state current density (ION ) up to ~ 1527 μA μm-1 and a mobility as high as ~ 690.7 cm2 V-1 s-1 at room temperature. Both Te phases exhibit good air stability after several months. Furthermore, short-channel (down to 46 nm) β-Te nanoribbon transistors exhibit remarkable electrical properties (ION = ~ 1270 μA μm-1 and ON-state resistance down to 0.63 kΩ μm) at Vds = 1 V., (© 2024. The Author(s).)- Published
- 2024
- Full Text
- View/download PDF
40. High intrinsic phase stability of ultrathin 2M WS 2 .
- Author
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Liu X, Zhang P, Wang S, Fang Y, Wu P, Xiang Y, Chen J, Zhao C, Zhang X, Zhao W, Wang J, Huang F, and Guan C
- Abstract
Metallic 2M or 1T'-phase transition metal dichalcogenides (TMDs) attract increasing interests owing to their fascinating physicochemical properties, such as superconductivity, optical nonlinearity, and enhanced electrochemical activity. However, these TMDs are metastable and tend to transform to the thermodynamically stable 2H phase. In this study, through systematic investigation and theoretical simulation of phase change of 2M WS
2 , we demonstrate that ultrathin 2M WS2 has significantly higher intrinsic thermal stabilities than the bulk counterparts. The 2M-to-2H phase transition temperature increases from 120 °C to 210 °C in the air as thickness of WS2 is reduced from bulk to bilayer. Monolayered 1T' WS2 can withstand temperatures up to 350 °C in the air before being oxidized, and up to 450 °C in argon atmosphere before transforming to 1H phase. The higher stability of thinner 2M WS2 is attributed to stiffened intralayer bonds, enhanced thermal conductivity and higher average barrier per layer during the layer(s)-by-layer(s) phase transition process. The observed high intrinsic phase stability can expand the practical applications of ultrathin 2M TMDs., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
41. Generating active metal/oxide reverse interfaces through coordinated migration of single atoms.
- Author
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Zhang L, Wan S, Du C, Wan Q, Pham H, Zhao J, Ding X, Wei D, Zhao W, Li J, Zheng Y, Xie H, Zhang H, Chen M, Zhang KHL, Wang S, Lin J, Huang J, Lin S, Wang Y, Datye AK, Wang Y, and Xiong H
- Abstract
Identification of active sites in catalytic materials is important and helps establish approaches to the precise design of catalysts for achieving high reactivity. Generally, active sites of conventional heterogeneous catalysts can be single atom, nanoparticle or a metal/oxide interface. Herein, we report that metal/oxide reverse interfaces can also be active sites which are created from the coordinated migration of metal and oxide atoms. As an example, a Pd
1 /CeO2 single-atom catalyst prepared via atom trapping, which is otherwise inactive at 30 °C, is able to completely oxidize formaldehyde after steam treatment. The enhanced reactivity is due to the formation of a Ce2 O3 -Pd nanoparticle domain interface, which is generated by the migration of both Ce and Pd atoms on the atom-trapped Pd1 /CeO2 catalyst during steam treatment. We show that the generation of metal oxide-metal interfaces can be achieved in other heterogeneous catalysts due to the coordinated mobility of metal and oxide atoms, demonstrating the formation of a new active interface when using metal single-atom material as catalyst precursor., (© 2024. The Author(s).)- Published
- 2024
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- View/download PDF
42. Thermal responses of dissolved organic matter under global change.
- Author
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Hu A, Jang KS, Tanentzap AJ, Zhao W, Lennon JT, Liu J, Li M, Stegen J, Choi M, Lu Y, Feng X, and Wang J
- Abstract
The diversity of intrinsic traits of different organic matter molecules makes it challenging to predict how they, and therefore the global carbon cycle, will respond to climate change. Here we develop an indicator of compositional-level environmental response for dissolved organic matter to quantify the aggregated response of individual molecules that positively and negatively associate with warming. We apply the indicator to assess the thermal response of sediment dissolved organic matter in 480 aquatic microcosms along nutrient gradients on three Eurasian mountainsides. Organic molecules consistently respond to temperature change within and across contrasting climate zones. At a compositional level, dissolved organic matter in warmer sites has a stronger thermal response and shows functional reorganization towards molecules with lower thermodynamic favorability for microbial decomposition. The thermal response is more sensitive to warming at higher nutrients, with increased sensitivity of up to 22% for each additional 1 mg L
-1 of nitrogen loading. The utility of the thermal response indicator is further confirmed by laboratory experiments and reveals its positive links to greenhouse gas emissions., (© 2024. The Author(s).)- Published
- 2024
- Full Text
- View/download PDF
43. Efficacy of Bifidobacterium animalis subsp. lactis BL-99 in the treatment of functional dyspepsia: a randomized placebo-controlled clinical trial.
- Author
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Zhang Q, Li G, Zhao W, Wang X, He J, Zhou L, Zhang X, An P, Liu Y, Zhang C, Zhang Y, Liu S, Zhao L, Liu R, Li Y, Jiang W, Wang X, Wang Q, Fang B, Zhao Y, Ren Y, Niu X, Li D, Shi S, Hung WL, Wang R, Liu X, and Ren F
- Subjects
- Humans, Feces microbiology, Double-Blind Method, Bifidobacterium animalis, Dyspepsia therapy, Probiotics therapeutic use
- Abstract
Current treatment for functional dyspepsia (FD) has limited and unsustainable efficacy. Probiotics have the sustainable potential to alleviate FD. This randomized controlled clinical trial (Chinese Clinical Trial Registry, ChiCTR2000041430) assigned 200 FD patients to receive placebo, positive-drug (rabeprazole), or Bifidobacterium animalis subsp. lactis BL-99 (BL-99; low, high doses) for 8-week. The primary outcome was the clinical response rate (CRR) of FD score after 8-week treatment. The secondary outcomes were CRR of FD score at other periods, and PDS, EPS, serum indicators, fecal microbiota and metabolites. The CRR in FD score for the BL-99_high group [45 (90.0%)] was significantly higher than that for placebo [29 (58.0%), p = 0.001], BL-99_low [37 (74.0%), p = 0.044] and positive_control [35 (70.0%), p = 0.017] groups after 8-week treatment. This effect was sustained until 2-week after treatment but disappeared 8-week after treatment. Further metagenomic and metabolomics revealed that BL-99 promoted the accumulation of SCFA-producing microbiota and the increase of SCFA levels in stool and serum, which may account for the increase of serum gastrin level. This study supports the potential use of BL-99 for the treatment of FD., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
44. FOXP3 + regulatory T cell perturbation mediated by the IFNγ-STAT1-IFITM3 feedback loop is essential for anti-tumor immunity.
- Author
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Liu X, Zhang W, Han Y, Cheng H, Liu Q, Ke S, Zhu F, Lu Y, Dai X, Wang C, Huang G, Su B, Zou Q, Li H, Zhao W, Xiao L, Lu L, Tong X, Pan F, Li H, and Li B
- Subjects
- Humans, Feedback, Cytokines metabolism, Forkhead Transcription Factors metabolism, Membrane Proteins metabolism, RNA-Binding Proteins metabolism, STAT1 Transcription Factor genetics, STAT1 Transcription Factor metabolism, T-Lymphocytes, Regulatory, Neoplasms genetics, Neoplasms therapy
- Abstract
Targeting tumor-infiltrating regulatory T cells (Tregs) is an efficient way to evoke an anti-tumor immune response. However, how Tregs maintain their fragility and stability remains largely unknown. IFITM3 and STAT1 are interferon-induced genes that play a positive role in the progression of tumors. Here, we showed that IFITM3-deficient Tregs blunted tumor growth by strengthening the tumor-killing response and displayed the Th1-like Treg phenotype with higher secretion of IFNγ. Mechanistically, depletion of IFITM3 enhances the translation and phosphorylation of STAT1. On the contrary, the decreased IFITM3 expression in STAT1-deficient Tregs indicates that STAT1 conversely regulates the expression of IFITM3 to form a feedback loop. Blocking the inflammatory cytokine IFNγ or directly depleting STAT1-IFITM3 axis phenocopies the restored suppressive function of tumor-infiltrating Tregs in the tumor model. Overall, our study demonstrates that the perturbation of tumor-infiltrating Tregs through the IFNγ-IFITM3-STAT1 feedback loop is essential for anti-tumor immunity and constitutes a targetable vulnerability of cancer immunotherapy., (© 2024. The Author(s).)
- Published
- 2024
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45. Author Correction: Submesoscale inverse energy cascade enhances Southern Ocean eddy heat transport.
- Author
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Zhang Z, Liu Y, Qiu B, Luo Y, Cai W, Yuan Q, Liu Y, Zhang H, Liu H, Miao M, Zhang J, Zhao W, and Tian J
- Published
- 2023
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46. Phylogeny and molecular evolution of the first local monkeypox virus cluster in Guangdong Province, China.
- Author
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Yu J, Zhang X, Liu J, Xiang L, Huang S, Xie X, Fang L, Lin Y, Zhang M, Wang L, He J, Zhang B, Di B, Peng B, Liang J, Shen C, Zhao W, and Li B
- Subjects
- Humans, Phylogeny, Disease Outbreaks, Evolution, Molecular, Monkeypox virus genetics, Mpox (monkeypox)
- Abstract
The first local mpox outbreak in Guangdong Province, China occurred in June 2023. However, epidemiological data have failed to quickly identify the source and transmission of the outbreak. Here, phylogeny and molecular evolution of 10 monkeypox virus (MPXV) genome sequences from the Guangdong outbreak were characterized, revealing local silent transmissions that may have occurred in Guangdong whose mpox outbreaks suggested a molecular epidemiological correlation with Portugal and several regions of China during the same period. The lineage IIb C.1, which includes all 10 MPXV from Guangdong, shows consistent temporal continuity in both phylogenetic characteristics and unique molecular evolutionary mutation spectrum, reflected in the continuous increase of single nucleotide polymorphisms (SNPs) and shared mutations over time. Compared with the Japan MPXV, the Guangdong MPXV showed higher genomic nucleotide differences and separated 14 shared mutations from the B.1 lineage, comprising 6 non-synonymous mutations in genes linked to host regulation, virus infection, and virus life cycle. The unique mutation spectrum with temporal continuity in IIb C.1, related to apolipoprotein B mRNA-editing catalytic polypeptide-like 3, promotes rapid viral evolution and diversification. The findings contribute to understanding the ongoing mpox outbreak in China and offer insights for developing joint prevention and control strategies., (© 2023. The Author(s).)
- Published
- 2023
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47. Topological electronic structure and spin texture of quasi-one-dimensional higher-order topological insulator Bi 4 Br 4 .
- Author
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Zhao W, Yang M, Xu R, Du X, Li Y, Zhai K, Peng C, Pei D, Gao H, Li Y, Xu L, Han J, Huang Y, Liu Z, Yao Y, Zhuang J, Du Y, Zhou J, Chen Y, and Yang L
- Abstract
The notion of topological insulators (TIs), characterized by an insulating bulk and conducting topological surface states, can be extended to higher-order topological insulators (HOTIs) hosting gapless modes localized at the boundaries of two or more dimensions lower than the insulating bulk. In this work, by performing high-resolution angle-resolved photoemission spectroscopy (ARPES) measurements with submicron spatial and spin resolution, we systematically investigate the electronic structure and spin texture of quasi-one-dimensional (1D) HOTI candidate Bi
4 Br4 . In contrast to the bulk-state-dominant spectra on the (001) surface, we observe gapped surface states on the (100) surface, whose dispersion and spin-polarization agree well with our ab-initio calculations. Moreover, we reveal in-gap states connecting the surface valence and conduction bands, which is a signature of the hinge states inside the (100) surface gap. Our findings provide compelling evidence for the HOTI phase of Bi4 Br4 . The identification of the higher-order topological phase promises applications based on 1D spin-momentum locked current in electronic and spintronic devices., (© 2023. The Author(s).)- Published
- 2023
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48. LncRNA INHEG promotes glioma stem cell maintenance and tumorigenicity through regulating rRNA 2'-O-methylation.
- Author
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Liu L, Liu Z, Liu Q, Wu W, Lin P, Liu X, Zhang Y, Wang D, Prager BC, Gimple RC, Yu J, Zhao W, Wu Q, Zhang W, Wu E, Chen X, Luo J, Rich JN, Xie Q, Jiang T, and Chen R
- Subjects
- Humans, Methylation, Ribonucleoproteins, Small Nucleolar metabolism, Neoplastic Stem Cells metabolism, Cell Line, Tumor, RNA, Long Noncoding genetics, RNA, Long Noncoding metabolism, Brain Neoplasms genetics, Brain Neoplasms metabolism, Glioma genetics, Glioma metabolism, Glioblastoma genetics, Glioblastoma metabolism
- Abstract
Glioblastoma (GBM) ranks among the most lethal of human cancers, containing glioma stem cells (GSCs) that display therapeutic resistance. Here, we report that the lncRNA INHEG is highly expressed in GSCs compared to differentiated glioma cells (DGCs) and promotes GSC self-renewal and tumorigenicity through control of rRNA 2'-O-methylation. INHEG induces the interaction between SUMO2 E3 ligase TAF15 and NOP58, a core component of snoRNP that guides rRNA methylation, to regulate NOP58 sumoylation and accelerate the C/D box snoRNP assembly. INHEG activation enhances rRNA 2
' -O-methylation, thereby increasing the expression of oncogenic proteins including EGFR, IGF1R, CDK6 and PDGFRB in glioma cells. Taken together, this study identifies a lncRNA that connects snoRNP-guided rRNA 2'-O-methylation to upregulated protein translation in GSCs, supporting an axis for potential therapeutic targeting of gliomas., (© 2023. The Author(s).)- Published
- 2023
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49. Precise solid-phase synthesis of CoFe@FeO x nanoparticles for efficient polysulfide regulation in lithium/sodium-sulfur batteries.
- Author
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Chen Y, Yao Y, Zhao W, Wang L, Li H, Zhang J, Wang B, Jia Y, Zhang R, Yu Y, and Liu J
- Abstract
Complex metal nanoparticles distributed uniformly on supports demonstrate distinctive physicochemical properties and thus attract a wide attention for applications. The commonly used wet chemistry methods display limitations to achieve the nanoparticle structure design and uniform dispersion simultaneously. Solid-phase synthesis serves as an interesting strategy which can achieve the fabrication of complex metal nanoparticles on supports. Herein, the solid-phase synthesis strategy is developed to precisely synthesize uniformly distributed CoFe@FeO
x core@shell nanoparticles. Fe atoms are preferentially exsolved from CoFe alloy bulk to the surface and then be carburized into a Fex C shell under thermal syngas atmosphere, subsequently the formed Fex C shell is passivated by air, obtaining CoFe@FeOx with a CoFe alloy core and a FeOx shell. This strategy is universal for the synthesis of MFe@FeOx (M = Co, Ni, Mn). The CoFe@FeOx exhibits bifunctional effect on regulating polysulfides as the separator coating layer for Li-S and Na-S batteries. This method could be developed into solid-phase synthetic systems to construct well distributed complex metal nanoparticles., (© 2023. The Author(s).)- Published
- 2023
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50. Local membrane source gathering by p62 body drives autophagosome formation.
- Author
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Feng X, Sun D, Li Y, Zhang J, Liu S, Zhang D, Zheng J, Xi Q, Liang H, Zhao W, Li Y, Xu M, He J, Liu T, Hasim A, Ma M, Xu P, and Mi N
- Subjects
- Macroautophagy, Phagosomes metabolism, Autophagy-Related Proteins genetics, Autophagy-Related Proteins metabolism, Lipids, Autophagosomes metabolism, Autophagy physiology
- Abstract
Autophagosomes are double-membrane vesicles generated intracellularly to encapsulate substrates for lysosomal degradation during autophagy. Phase separated p62 body plays pivotal roles during autophagosome formation, however, the underlying mechanisms are still not fully understood. Here we describe a spatial membrane gathering mode by which p62 body functions in autophagosome formation. Mass spectrometry-based proteomics reveals significant enrichment of vesicle trafficking components within p62 body. Combining cellular experiments and biochemical reconstitution assays, we confirm the gathering of ATG9 and ATG16L1-positive vesicles around p62 body, especially in Atg2ab DKO cells with blocked lipid transfer and vesicle fusion. Interestingly, p62 body also regulates ATG9 and ATG16L vesicle trafficking flux intracellularly. We further determine the lipid contents associated with p62 body via lipidomic profiling. Moreover, with in vitro kinase assay, we uncover the functions of p62 body as a platform to assemble ULK1 complex and invigorate PI3KC3-C1 kinase cascade for PI3P generation. Collectively, our study raises a membrane-based working model for multifaceted p62 body in controlling autophagosome biogenesis, and highlights the interplay between membraneless condensates and membrane vesicles in regulating cellular functions., (© 2023. The Author(s).)
- Published
- 2023
- Full Text
- View/download PDF
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