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基于蛋白质沉淀的药物靶点筛选方法的研究进展

刘彤 秦伟捷 杨洪军

色谱2024,Vol.42Issue(7):613-622,10.
色谱2024,Vol.42Issue(7):613-622,10.DOI:10.3724/SP.J.1123.2023.11019

基于蛋白质沉淀的药物靶点筛选方法的研究进展

Recent advances in protein precipitation-based methods for drug-target screening

刘彤 1秦伟捷 2杨洪军3

作者信息

  • 1. 中国中医科学院医学实验中心,中医药防治重大疾病基础研究北京市重点实验室,北京 100700||医学蛋白质组全国重点实验室,国家蛋白质科学中心(北京),北京蛋白质组研究中心,军事科学院军事医学研究院,北京 102206
  • 2. 医学蛋白质组全国重点实验室,国家蛋白质科学中心(北京),北京蛋白质组研究中心,军事科学院军事医学研究院,北京 102206
  • 3. 中国中医科学院医学实验中心,中医药防治重大疾病基础研究北京市重点实验室,北京 100700
  • 折叠

摘要

Abstract

Drug targets are biological macromolecules that bind drug molecules in vivo.There-fore,the system-wide identification of drug targets plays a vital role in fully understanding the mechanism of drug action,efficacy,and side effects.The unbiased screening of drug targets may accelerate the process of drug discovery and candidate screening.Mass spectrometry is a key tool for large-scale protein identification and accurate quantification owing to its high acqui-sition speed,resolution,and sensitivity.Mass spectrometry-based proteomics has been widely used for drug-target screening.It can systematically identify the protein-target landscape of a drug and elucidate drug-protein interactions.Commonly used drug-target characterization meth-ods,such as labeling-based affinity enrichment,require the chemical derivatization of drug molecules,which is not only time-consuming but may also affect the affinity of the drug to-wards its targets.Furthermore,the spatial effects of the derivatization groups may block inter-actions between the drug and its targets.Considering the disadvantages of affinity-enrichment methods,strategies that do not require chemical derivatization have received widespread atten-tion.Proteins may undergo denaturation,unfolding,and precipitation under different condi-tions such as high temperatures,extreme pH,denaturants,and mechanical stress.Binding to small-molecule drugs may alter the folding balance of target proteins.The conformational stabil-ity of target proteins can be stabilized by binding with drugs,and protein-drug complexes are more resistant than free proteins to the precipitation induced by different conditions.Based on this mechanism,various large-scale drug-target identification methods using protein precipitati-on have been developed by combining proteomics and mass spectrometry analysis,including thermal proteome profiling and solvent-,mechanical stress-,and pH-induced protein precipita-tion.These methods have been successfully applied to the characterization of small-molecule drug targets.In this review,we describe the protein precipitation-based methods used for the high-throughput discovery of drug targets and elucidation of the interactions between drugs and proteins in the past decade.We also summarize the characteristics of each method and discuss their application potential in drug-efficacy evaluation and drug discovery.

关键词

生物质谱/药靶鉴定/蛋白质沉淀/蛋白质组学

Key words

biomass spectrometry/drug target identification/protein precipitation/proteomics

分类

化学化工

引用本文复制引用

刘彤,秦伟捷,杨洪军..基于蛋白质沉淀的药物靶点筛选方法的研究进展[J].色谱,2024,42(7):613-622,10.

基金项目

中国中医科学院科技创新项目(CI2021B017) (CI2021B017)

中国博士后科学基金项目(2023T160727).Scientific and Technological Innovation Project of China Academy of Chinese Medical Sciences(No.CI2021B017) (2023T160727)

China Postdoctoral Science Foundation(No.2023T160727). (No.2023T160727)

色谱

OA北大核心CSTPCDMEDLINE

1000-8713

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