排序方式: 共有91条查询结果,搜索用时 46 毫秒
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Liang Cui Yanling Song Guoliang Ke Zhichao Guan Huimin Zhang Ya Lin Yishun Huang Dr. Zhi Zhu Prof. Chaoyong James Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(32):10442-10451
Recently, the binding ability of DNA on GO and resulting nuclease resistance have attracted increasing attention, leading to new applications both in vivo and in vitro. In vivo, nucleic acids absorbed on GO can be effectively protected from enzymatic degradation and biological interference in complicated samples, making it useful for targeted delivery, gene regulation, intracellular detection and imaging with high uptake efficiencies, high intracellular stability, and very low toxicity. In vitro, the adsorption of ssDNA on GO surface and desorption of dsDNA or well‐folded ssDNA from GO surface result in the protection and deprotection of DNA from nucleic digestion, respectively, which has led to target‐triggered cyclic enzymatic amplification methods (CEAM) for amplified detection of analytes with sensitivity 2–3 orders of magnitude higher than that of 1:1 binding strategies. This Concept article explores some of the latest developments in this field. 相似文献
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Mengjiao Huang Dr. Juanjuan Yang Teng Wang Dr. Jia Song Jinglu Xia Dr. Lingling Wu Dr. Wei Wang Dr. Qiaoyi Wu Prof. Zhi Zhu Dr. Yanling Song Prof. Chaoyong Yang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(12):4830-4835
Immunotherapy has revolutionized cancer treatment, but its efficacy is severely hindered by the lack of effective predictors. Herein, we developed a homogeneous, low-volume, efficient, and sensitive exosomal programmed death-ligand 1 (PD-L1, a type of transmembrane protein) quantitation method for cancer diagnosis and immunotherapy response prediction (HOLMES-ExoPD-L1). The method combines a newly evolved aptamer that efficiently binds to PD-L1 with less hindrance by antigen glycosylation than antibody, and homogeneous thermophoresis with a rapid binding kinetic. As a result, HOLMES-ExoPD-L1 is higher in sensitivity, more rapid in reaction time, and easier to operate than existing enzyme-linked immunosorbent assay (ELISA)-based methods. As a consequence of an outstanding improvement of sensitivity, the level of circulating exosomal PD-L1 detected by HOLMES-ExoPD-L1 can effectively distinguish cancer patients from healthy volunteers, and for the first time was found to correlate positively with the metastasis of adenocarcinoma. Overall, HOLMES-ExoPD-L1 brings a fresh approach to exosomal PD-L1 quantitation, offering unprecedented potential for early cancer diagnosis and immunotherapy response prediction. 相似文献
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Zhi Zhu Zhichao Guan Dan Liu Shasha Jia Jiuxing Li Zhichao Lei Shuichao Lin Tianhai Ji Zhongqun Tian Chaoyong James Yang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(36):10594-10599
Herein, we demonstrate that a very familiar, yet underutilized, physical parameter—gas pressure—can serve as signal readout for highly sensitive bioanalysis. Integration of a catalyzed gas‐generation reaction with a molecular recognition component leads to significant pressure changes, which can be measured with high sensitivity using a low‐cost and portable pressure meter. This new signaling strategy opens up a new way for simple, portable, yet highly sensitive biomedical analysis in a variety of settings. 相似文献
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Molecular orbital calculations of some extended sesquifulvalene compounds as On with olefins bridge and Tn with thiophenes bridge as well as their corresponding cyclopentadienyl‐iron(II) coordination compounds as IOn and ITn at the hybrid density functional theory level demonstrate that the dipole moment depends linearly on the molecular size (n), and the linear polarizability depends linearly on n2 as well as the first hyperpolarizability also has a linear dependence on n3. 相似文献
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Hao Zheng Quanjiang Li Chaoyong Yu Xue Zhu Pinting Guo Yuanyuan Mu Lichun Ma 《先进技术聚合物》2019,30(3):620-630
A simple and efficient chemical method was developed to graft directly carbon nanofibers (CNFs) onto carbon fiber (CF) surface to construct a CF‐CNF hierarchical reinforcing structure. The grafted CF reinforcements via covalent ester linkage at low temperature without any usage of dendrimer or catalyst was investigated by FTIR, X‐ray photoelectron spectroscopy, Raman, scanning electron microscopy, atomic force microscopy, dynamic contact angle analysis, and single fiber tensile testing. The results indicated that the CNFs with high density could effectively increase the polarity, wettability, and roughness of the CF surface. Simultaneous enhancements of the interfacial shear strength, flexural strength, and dynamic mechanical properties as well as the tensile strength of CFs were achieved, for an increase of 75.8%, 21.9%, 21.7%, and 0.5%, respectively. We believe the facile and effective method may provide a novel and promising interface design strategy for next‐generation advanced composite structures. 相似文献
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Monitoring gene expression in vivo is essential to the advancement of biological studies, medical diagnostics, and drug discovery.
Adding to major efforts in developing molecular probes for mRNA monitoring, we have recently developed an alternative tool,
the hybrid molecular probe (HMP). To optimize the probe, a series of experiments were performed to study the properties of
HMP hybridization kinetics and stability. The results demonstrated the potential of the HMP as a prospective tool for use
in both hybridization studies and in vitro and in vivo analyses. The HMP has shown no tendency to produce false positive signals,
which is a major concern for living cell studies. Moreover, HMP has shown the ability to detect the mRNA expression of different
genes inside single cells from both basal and stimulated genes. As an effective alternative to conventional molecular probes,
the proven sensitivity, simplicity, and stability of HMPs show promise for their use in monitoring mRNA expression in living
cells.
Figure Hybrid molecular probe (HMP). HMPs consist of two single strands of DNA (green) and a polyethylene glycol (PEG, purple) linker that is used to tether these two sequences together. When a target (orange strand) containing the complementary sequences to both probes at adjacent positions is added, each strand binds to its corresponding
target sequence, thus bringing the two fluorophores into close proximity, which allows energy transfer to occur 相似文献