Search

Although sulfurated polymers promise unique properties, their controlled synthesis, particularly when it comes to complex and functional architectures, remains challenging. Here, we show that the copolymerization of oxetane and phenyl isothiocyanate selectively yields polythioimidocarbonates as a new class of sulfur containing polymers, with narrow molecular weight distributions (Mn=5–80 kg/mol with Đ≤1.2; Mn,max=124 kg/mol) and high melting points of up to 181 °C. The method tolerates different substituent patterns on both the oxetane and the isothiocyanate. Self‐nucleation experiments reveal that π‐stacking of phenyl substituents, the presence of unsubstituted polymer backbones, and the kinetically controlled linkage selectivity are key factors in maximising melting points. The increased tolerance to macro‐chain transfer agents and the controlled propagation allows the synthesis of double crystalline and amphiphilic diblock copolymers, which can be assembled into micellar‐ and worm‐like structures with amorphous cores in water. In contrast, crystallization driven self‐assembly in ethanol gives cylindrical micelles or platelets. [ABSTRACT FROM AUTHOR]

A recent research article in Angewandte Chemie by Alex J. Plajer et al. discusses the easy synthesis of sulfur-containing polymers with high melting points. The authors demonstrate that these polymers can be obtained through the copolymerization of phenylisothiocyanate and oxetane. Additionally, the resulting polythioimidocarbonate can be used as a core-forming block in the self-assembly of a diblock copolymer. This research provides valuable insights into the synthesis and potential applications of sulfurated copolymers. [Extracted from the article]

Herein, epitaxially regrown n+ (In)GaN source/drain layers for radio frequency high electron mobility transistors, addressing material and electrical characterization, are reported. A range of n+ GaN and n+ InGaN layers with indium 4–12 at% and silicon 0–5.1 × 1020 cm−3 are evaluated. The active carrier concentration in n+ InGaN exceeds 2 × 1020 cm−3. The layers exhibit so‐called V‐defects, observed by atomic force microscope and transmission electron microscope (TEM), which are associated with local composition changes. In addition to the high Si doping levels, nitrogen vacancies are also considered to contribute toward their net carrier concentration. Due to its relevance for device processing, selectivity analysis is performed, and the optimal process conditions for selective regrowth are identified. Regrowth under high temperature (800 °C) is found to be conducive to improved selectivity. However, a high thermal budget negatively impacts the overall regrowth process, as reported here for In0.17Al0.83N and Al0.26Ga0.74N barriers: whereas the InAlN barrier suffers from intermixing, the AlGaN barrier demonstrates high‐temperature stability. The impact of intermixing is studied from complementary TEM and DC electrical measurements. A low overall contact resistance of 75 Ω μm is obtained with the regrown n+ InGaN layers. [ABSTRACT FROM AUTHOR]

Prime editors make programmed genome modifications by writing new sequences into extensions of nicked DNA 3' ends. These edited 3' new strands must displace competing 5' strands to install edits, yet a bias toward retaining the competing 5' strands hinders efficiency and can cause indel errors. Using rational design of the constituent Cas9-nickase to reposition prime editor nicks, we discovered that competing 5' strands are destabilized to favor the edited 3' new strands. We exploit this mechanism to engineer efficient prime editors with strikingly low indel errors. Combining this error-suppressing strategy with the latest efficiency-boosting architecture, we design a next- generation prime editor (vPE). Compared with previous editors, vPE features comparable efficiency yet up to 60-fold lower indel errors, enabling edit:indel ratios as high as 465:1., One Sentence Summary: Prime editors designed with repositioned DNA breaks nearly eliminate undesired genome editing errors.

Although sulfurated polymers promise unique properties, their controlled synthesis, particularly when it comes to complex and functional architectures, remains challenging. Here, we show that the copolymerization of oxetane and phenyl isothiocyanate selectively yields polythioimidocarbonates as a new class of sulfur containing polymers, with narrow molecular weight distributions (M n =5-80 kg/mol with Đ≤1.2; M n,max =124 kg/mol) and high melting points of up to 181 °C. The method tolerates different substituent patterns on both the oxetane and the isothiocyanate. Self-nucleation experiments reveal that π-stacking of phenyl substituents, the presence of unsubstituted polymer backbones, and the kinetically controlled linkage selectivity are key factors in maximising melting points. The increased tolerance to macro-chain transfer agents and the controlled propagation allows the synthesis of double crystalline and amphiphilic diblock copolymers, which can be assembled into micellar- and worm-like structures with amorphous cores in water. In contrast, crystallization driven self-assembly in ethanol gives cylindrical micelles or platelets., (© 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

Patient-specific, human-based cellular models integrating a biomimetic blood-brain barrier (BBB), immune, and myelinated neuron components are critically needed to enable accelerated, translationally relevant discovery of neurological disease mechanisms and interventions. By engineering a novel brain-mimicking 3D hydrogel and co-culturing all six major brain cell types derived from patient iPSCs, we have constructed, characterized, and utilized a multicellular integrated brain (miBrain) immuno-glial-neurovascular model with in vivo- like hallmarks inclusive of neuronal activity, functional connectivity, barrier function, myelin-producing oligodendrocyte engagement with neurons, multicellular interactions, and transcriptomic profiles. We implemented the model to study Alzheimer's Disease pathologies associated with APOE4 genetic risk. APOE4 miBrains differentially exhibit amyloid aggregation, tau phosphorylation, and astrocytic GFAP. Unlike the co-emergent fate specification of glia and neurons in organoids, miBrains integrate independently differentiated cell types, a feature we harnessed to identify that APOE4 in astrocytes promotes neuronal tau pathogenesis and dysregulation through crosstalk with microglia.

The transplantation of engineered cells that secrete therapeutic proteins presents a promising method for addressing a range of chronic diseases. However, hydrogels used to encase and protect non-autologous cells from immune rejection often suffer from poor mechanical properties, insufficient oxygenation, and fibrotic encapsulation. Here, we introduce a composite encapsulation system comprising an oxygen-permeable silicone cryogel skeleton, a hydrogel matrix, and a fibrosis-resistant polymer coating. Cryogel skeletons enhance the fracture toughness of conventional alginate hydrogels by 23-fold and oxygen diffusion by 2.8-fold, effectively mitigating both implant fracture and hypoxia of encapsulated cells. Composite implants containing xenogeneic cells engineered to secrete erythropoietin significantly outperform unsupported alginate implants in therapeutic delivery over 8 weeks in immunocompetent mice. By improving mechanical resiliency and sustaining denser cell populations, silicone cryogel skeletons enable more durable and miniaturized therapeutic implants.