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Multifunctional molecular switches have attracted much attention because of their unique stimulus response behavior and advanced applications. However, precise regulation of the structure for property enrichment is still a great challenge. Herein, the first case of a single‐molecule switch BN‐S with multiple structurally tunable and full‐color fluorescent properties is reported. Interestingly, BN‐S exhibits a butterfly‐like "metamorphosis" crystal growth process accompanied by full‐color fluorescence emission (including white light, CIE = 0.33, 0.33; 456 nm → 610 nm). It is shown that this is related to the reversible B←N bonding and the tunability of the spatial structure of the BN‐S. Thus, BN‐S exhibits superior multicolor tunability in different states (solid, liquid, and film), and its applications in white‐light optical light emitting diodes (OLEDs) and multicolor fluorescent inks also show great promise. This will provide a new strategy for designing and synthesizing the development of multifunctional molecular switching materials and enriching the variety of organoboron luminescent materials. [ABSTRACT FROM AUTHOR]

Summary: The nuclear factor Y (NF‐Y) transcription factors play important roles in plant development and physiological responses. However, the relationship between NF‐Y, plant hormone and plant stress resistance in tropical crops remains unclear. In this study, we identified MeNF‐YC15 gene in the NF‐Y family that significantly responded to Xanthomonas axonopodis pv. manihotis (Xam) treatment. Using MeNF‐YC15‐silenced and ‐overexpressed cassava plants, we elucidated that MeNF‐YC15 positively regulated disease resistance to cassava bacterial blight (CBB). Notably, we illustrated MeNF‐YC15 downstream genes and revealed the direct genetic relationship between MeNF‐YC15 and 1‐aminocyclopropane‐1‐carboxylic acid (ACC) oxidase (MeACO1)‐ethylene module in disease resistance, as evidenced by the rescued disease susceptibility of MeNF‐YC15 silenced cassava plants with ethylene treatment or overexpressing MeACO1. In addition, the physical interaction between 2C‐type protein phosphatase 1 (MePP2C1) and MeNF‐YC15 inhibited the transcriptional activation of MeACO1 by MeNF‐YC15. In summary, MePP2C1‐MeNF‐YC15 interaction modulates ethylene biosynthesis and cassava disease resistance, providing gene network for cassava genetic improvement. [ABSTRACT FROM AUTHOR]

High-pressure pure waterjet (WJ) technology is widely used in the hole drilling process for carbon fiber–reinforced polymers (CFRP) laminates because of its high processing efficiency and zero heat affected zones. However, the phenomena of the delamination zone and poor roundness pose significant challenges to the hole processing of CFRP laminates. In this study, the numerical and experimental investigation of a high-pressure pure WJ CFRP laminate drilling process are conducted, to improve the quality of the pure WJ drilling process. A comprehensive coupled fluid–solid numerical model based on the smoothed particle hydrodynamics method is developed to simulate the pure WJ drilling process of CFRP laminates and determine mechanism of the material removal. Thereafter, extensive pure WJ drilling experiments are conducted on two stacking sequence CFRP laminates to obtain a hole with remarkable roundness. The simulation results illustrate that during the WJ drilling of CFRP laminates, the material removal process and damage zones of each inter-laminate interface are mainly extended along the fiber direction (the direction of longitudinal Young's modulus). Water-wedging action is observed to play an important role in the damage of inter-laminate interface and propagation of peel-up and push-down delamination. Furthermore, the experimental results show that an increase in the WJ pressure contributes to the reduced hole taper and surface roughness of sidewalls. Holes with diameters below 2 mm are successfully drilled, and a roundness error of 0.05 mm is obtained for the [0/45/–45/90]2s CFRP laminate, which is 1/6 of that of the [0]16 laminate. [ABSTRACT FROM AUTHOR]

As information messengers for cell‐to‐cell communication, exosomes, typically small membrane vesicles (30–150 nm), play an imperative role in the physiological and pathological processes of living systems. Accumulating studies have demonstrated that exosomes are potential biological candidates for theranostics, including liquid biopsy‐based diagnosis and drug delivery. However, their clinical applications are hindered by several issues, especially their unspecific detection and insufficient targeting ability. How to upgrade the accuracy of exosome‐based theranostics is being widely explored. Aptamers, benefitting from their admirable characteristics, are used as excellent molecular recognition elements to empower exosomes for precision theranostics. With high affinity against targets and easy site‐specific modification, aptamers can be incorporated with platforms for the specific detection of exosomes, thus providing opportunities for advancing disease diagnostics. Furthermore, aptamers can be tailored and functionalized on exosomes to enable targeted therapeutics. Herein, this review emphasizes the empowering of exosomes by aptamers for precision theranostics. A brief introduction of exosomes and aptamers is provided, followed by a discussion of recent progress in aptamer‐based exosome detection for disease diagnosis, and the emerging applications of aptamer‐functionalized exosomes for targeted therapeutics. Finally, current challenges and opportunities in this research field are presented. [ABSTRACT FROM AUTHOR]

Organic radical luminescent materials have attracted worldwide attention because of their absolute spin‐allowed radiative transition and sensitivity to the environment, which give it multiple stimulus response properties. Nowadays, how to regulate and utilize the sensitivity of radicals has become a hot and difficult issue. Here, arylphosphonium bromide salts are introduced into the molecular backbone of naphthimide (NMI) using an intramolecular counterion strategy, and prepared a novel multifunctional stabilized radical luminescent: TPP‐o‐3OMe‐NMI‐Br. Interestingly, this molecule exhibits different assembly modes in different solvents, resulting in the generation of two crystals with different fluorescence (green: G‐C; orange–yellow: Y‐C), in which the Y‐C crystalline powder exhibits excellent stabilization properties for doublet and triplet excitons, which induce the emission of orange–yellow radical afterglow, and exhibits multi‐stimuli responsiveness to external pressure (P), temperature (T) and water (W). Moreover, interesting time‐dependent photoactivated colorful fluorescence and orange–yellow radical afterglow can be observed in TPP‐o‐3OMe‐NMI‐Br@PMMA films with different doping ratios and exhibit multi‐color tunability, multiple stimulus responses, multiple data encryption, and optical information erase/write behavior. This study not only broadens the types and applications of organic radical long afterglow materials but also provides new ideas for designing new organic "chameleon" luminescent materials in the field of smart luminescence materials. [ABSTRACT FROM AUTHOR]

Molecular profiling of protein markers on small extracellular vesicles (sEVs) is a promising strategy for the precise detection and classification of ovarian cancers. However, this strategy is challenging owing to the lack of simple and practical detection methods. In this work, using an aptamer‐based nanoflow cytometry (nFCM) detection strategy, a simple and rapid method for the molecular profiling of multiple protein markers on sEVs was developed. The protein markers can be easily labeled with aptamer probes and then rapidly profiled by nFCM. Seven cancer‐associated protein markers, including CA125, STIP1, CD24, EpCAM, EGFR, MUC1, and HER2, on plasma sEVs were profiled for the molecular detection and classification of ovarian cancers. Profiling these seven protein markers enabled the precise detection of ovarian cancer with a high accuracy of 94.2 %. In addition, combined with machine learning algorithms, such as linear discriminant analysis (LDA) and random forest (RF), the molecular classifications of ovarian cancer cell lines and subtypes were achieved with overall accuracies of 82.9 % and 55.4 %, respectively. Therefore, this simple, rapid, and non‐invasive method exhibited considerable potential for the auxiliary diagnosis and molecular classification of ovarian cancers in clinical practice. [ABSTRACT FROM AUTHOR]

Recently emerging perovskite nanocrystals (PNCs) have drawn considerable attention due to the superior optoelectronic performances. However, the terrible stability of red emissive PNCs (r‐PNCs) limits their broader application in aqueous media. Despite various encapsulation methods are proposed, the preparation of aqueous r‐PNCs with facile operation and excellent durability is still challenging. Herein, aqueous green emissive PNCs (g‐PNCs) by employing water as an external stimulus to treat oleyamine‐capped CsPbBr3 PNCs are synthesized initially, and then aqueous‐stable pure red emissive PNCs by anion‐exchange reaction and subsequently thiocyanate (SCN‐) passivation treatment (SCN‐r‐PNCs) are prepared. The obtained aqueous‐stable SCN‐r‐PNCs display high brightness, outstanding stability, and extended photoluminescence lifetime. Moreover, by combining aqueous r‐PNCs and portable smartphones, a fluorescence chemosensor for the detection of aqueous SCN− ions is constructed, which exhibits simple operation, high sensitivity, high selectivity, low detection limit, and visualized sensing. This work not only provides a new and facile strategy to prepare aqueous‐stable red emissive PNCs, but also further extends the application of red emissive PNCs in aqueous‐based fields. [ABSTRACT FROM AUTHOR]