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利用基于活性的探针鉴定具有活性的小分子的细胞靶标。

Identifying the cellular targets of bioactive small molecules with activity-based probes.

机构信息

ZJU-ENS Joint Laboratory of Medicinal Chemistry, College of Pharmaceutical Sciences, Zhejiang University, 388 Yuhangtang Road Hang-Zhou, Zhejiang Province 310058, PR China.

出版信息

Curr Med Chem. 2010;17(27):3030-44. doi: 10.2174/092986710791959747.

Abstract

The renaissance of cell- or organism-based phenotypic assays has made subsequent target identification for bioactive small organic molecules an important aspect of current drug discovery. Among the many strategies available for target identification, derivatizing bioactive small molecules into activity-based probes has the main advantage of determining small molecule-protein interactions directly in the native environment where the target proteins maintain their three-dimensional structures, including all the post-translational modifications, as the discrete small molecular probes usually have better access to intracellular compartments. Thus this chemical platform will not only afford a more precise means of understanding the mechanisms of action for bioactive molecules, but shed light onto the specificity of the bioactive small molecules. Here we will provide an overview of the strategies for the design of activity-based small molecular probes and review their applications for target identification using case studies. Special emphasis is placed on logistic concerns for probe's design as well as recent developments in this field.

摘要

基于细胞或生物体的表型分析的复兴使得生物活性小分子的后续靶标鉴定成为当前药物发现的一个重要方面。在可用的许多靶标鉴定策略中,将生物活性小分子衍生为基于活性的探针具有主要的优势,因为它可以直接在靶蛋白保持其三维结构的天然环境中确定小分子-蛋白质相互作用,包括所有的翻译后修饰,因为离散的小分子探针通常更容易进入细胞内区室。因此,这个化学平台不仅将提供一种更精确的手段来理解生物活性分子的作用机制,而且还将揭示生物活性小分子的特异性。在这里,我们将提供一个基于活性的小分子探针设计策略的概述,并通过案例研究回顾它们在靶标鉴定中的应用。特别强调了探针设计的逻辑问题以及该领域的最新发展。

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