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使用超分子化学传感器的酶分析——无标记方法。

Enzyme assays with supramolecular chemosensors - the label-free approach.

作者信息

Nilam Mohamed, Hennig Andreas

机构信息

Department of Biology/Chemistry, Center for Cellular Nanoanalytics (CellNanOs), Universität Osnabrück Barbarastr. 7 D-49076 Osnabrück Germany

出版信息

RSC Adv. 2022 Apr 6;12(17):10725-10748. doi: 10.1039/d1ra08617k. eCollection 2022 Mar 31.

Abstract

Enzyme activity measurements are essential for many research areas, , for the identification of inhibitors in drug discovery, in bioengineering of enzyme mutants for biotechnological applications, or in bioanalytical chemistry as parts of biosensors. In particular in high-throughput screening (HTS), sensitive optical detection is most preferred and numerous absorption and fluorescence spectroscopy-based enzyme assays have been developed, which most frequently require time-consuming fluorescent labelling that may interfere with biological recognition. The use of supramolecular chemosensors, which can specifically signal analytes with fluorescence-based read-out methods, affords an attractive and label-free alternative to more established enzyme assays. We provide herein a comprehensive review that summarizes the current state-of-the-art of supramolecular enzyme assays ranging from early examples with covalent chemosensors to the most recent applications of supramolecular tandem enzyme assays, which utilize common and often commercially available combinations of macrocyclic host molecules ( cyclodextrins, calixarenes, and cucurbiturils) and fluorescent dyes as self-assembled reporter pairs for assaying enzyme activity.

摘要

酶活性测量对于许多研究领域至关重要,例如在药物研发中鉴定抑制剂、在酶突变体的生物工程以用于生物技术应用,或者在作为生物传感器一部分的生物分析化学中。特别是在高通量筛选(HTS)中,灵敏的光学检测是最受青睐的,并且已经开发了许多基于吸收和荧光光谱的酶测定方法,这些方法最常需要耗时的荧光标记,而这可能会干扰生物识别。超分子化学传感器的使用,其可以通过基于荧光的读出方法特异性地对分析物发出信号,为更成熟的酶测定方法提供了一种有吸引力的无标记替代方案。我们在此提供一篇全面的综述,总结了超分子酶测定的当前技术水平,范围从早期使用共价化学传感器的例子到超分子串联酶测定的最新应用,后者利用大环主体分子(环糊精、杯芳烃和葫芦脲)和荧光染料的常见且通常是商业可得的组合作为自组装报告对来测定酶活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6d/8984408/218b0b9e0586/d1ra08617k-f1.jpg

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