化学蛋白质组学驱动的治疗目标识别和药物发现

Biology Pub Date : 2024-07-23 DOI:10.3390/biology13080555
Mingjie Zou, Haiyuan Zhou, Letian Gu, Jingzi Zhang, Lei Fang
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引用次数: 0

摘要

在人的一生中,从受孕到生命终结,小分子与许多生理过程都有着内在的联系。对小分子靶点的研究对药理学发现具有重要意义。确定小分子药物的作用位点有助于阐明小分子药物的药效学和毒理学机制,有助于阐明药物的脱靶效应和抗药性机制。因此,近年来研究小分子靶标的创新方法层出不穷,其中化学蛋白质组学是后基因组时代化学生物学发展的先锋。化学蛋白质组学可以在复杂的生物基质中非选择性地识别化合物的未知靶标,探针和非探针模式都能实现有效的靶标识别。本综述试图总结通过化学蛋白质组学鉴定小分子靶标的方法和示例。它深入探讨了小分子与人体生物学之间的相互作用,为发现和理解新型药物以及改进药物安全性评估提供了重要的方向和策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Target Identification and Drug Discovery Driven by Chemical Proteomics
Throughout the human lifespan, from conception to the end of life, small molecules have an intrinsic relationship with numerous physiological processes. The investigation into small-molecule targets holds significant implications for pharmacological discovery. The determination of the action sites of small molecules provide clarity into the pharmacodynamics and toxicological mechanisms of small-molecule drugs, assisting in the elucidation of drug off-target effects and resistance mechanisms. Consequently, innovative methods to study small-molecule targets have proliferated in recent years, with chemical proteomics standing out as a vanguard development in chemical biology in the post-genomic age. Chemical proteomics can non-selectively identify unknown targets of compounds within complex biological matrices, with both probe and non-probe modalities enabling effective target identification. This review attempts to summarize methods and illustrative examples of small-molecule target identification via chemical proteomics. It delves deeply into the interactions between small molecules and human biology to provide pivotal directions and strategies for the discovery and comprehension of novel pharmaceuticals, as well as to improve the evaluation of drug safety.
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