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酶的底物选择性小分子调节剂:机制与机遇。

Substrate-selective small-molecule modulators of enzymes: Mechanisms and opportunities.

机构信息

Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.

出版信息

Curr Opin Chem Biol. 2023 Feb;72:102231. doi: 10.1016/j.cbpa.2022.102231. Epub 2022 Nov 28.

Abstract

Small-molecule inhibitors of enzymes are widely used tools in reverse chemical genetics to probe biology and explore therapeutic opportunities. They are often compared with genetic knockdown or knockout and are expected to produce phenotypes similar to the genetic perturbations. This review aims to highlight that small molecule inhibitors of enzymes and genetic perturbations may not necessarily produce the same phenotype due to the possibility of substrate-selective or substrate-dependent effects of the inhibitors. Examples of substrate-selective inhibitors and the mechanisms for the substrate-selective effects are discussed. Substrate-selective modulators of enzymes have distinct advantages and cannot be easily replaced with biologics. Thus, they present an exciting opportunity for chemical biologists and medicinal chemists.

摘要

酶的小分子抑制剂在反向化学遗传学中被广泛用作研究生物学和探索治疗机会的工具。它们通常与基因敲低或敲除进行比较,并期望产生与遗传扰动相似的表型。本综述旨在强调,由于抑制剂可能具有底物选择性或底物依赖性作用,因此酶的小分子抑制剂和遗传扰动不一定会产生相同的表型。讨论了底物选择性抑制剂的例子和底物选择性作用的机制。酶的底物选择性调节剂具有明显的优势,并且不能轻易地被生物制剂所替代。因此,它们为化学生物学家和药物化学家提供了一个令人兴奋的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5459/9870951/22c9411d0921/nihms-1853796-f0027.jpg

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