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从表型命中到化学探针:阐明小分子在复杂生物系统中作用的化学生物学方法。

From Phenotypic Hit to Chemical Probe: Chemical Biology Approaches to Elucidate Small Molecule Action in Complex Biological Systems.

机构信息

Department of Organic Chemistry, University of Geneva, Quai Ernest-Ansermet 30, 1211 Genève, Switzerland.

出版信息

Molecules. 2020 Dec 3;25(23):5702. doi: 10.3390/molecules25235702.

Abstract

Biologically active small molecules have a central role in drug development, and as chemical probes and tool compounds to perturb and elucidate biological processes. Small molecules can be rationally designed for a given target, or a library of molecules can be screened against a target or phenotype of interest. Especially in the case of phenotypic screening approaches, a major challenge is to translate the compound-induced phenotype into a well-defined cellular target and mode of action of the hit compound. There is no "one size fits all" approach, and recent years have seen an increase in available target deconvolution strategies, rooted in organic chemistry, proteomics, and genetics. This review provides an overview of advances in target identification and mechanism of action studies, describes the strengths and weaknesses of the different approaches, and illustrates the need for chemical biologists to integrate and expand the existing tools to increase the probability of evolving screen hits to robust chemical probes.

摘要

生物活性小分子在药物开发中起着核心作用,是用于干扰和阐明生物过程的化学探针和工具化合物。小分子可以针对特定的靶点进行合理设计,也可以针对感兴趣的靶点或表型对文库中的分子进行筛选。特别是在表型筛选方法的情况下,一个主要的挑战是将化合物诱导的表型转化为明确的细胞靶点和命中化合物的作用模式。没有一种方法适用于所有情况,近年来,基于有机化学、蛋白质组学和遗传学的靶标解析策略不断增加。本文综述了靶标鉴定和作用机制研究方面的进展,描述了不同方法的优缺点,并说明了化学生物学家需要整合和扩展现有工具,以增加将筛选命中物演化为稳健化学探针的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978c/7730769/7292e466db6f/molecules-25-05702-g001.jpg

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