School of Chemistry, University of Edinburgh, West Mains Road, Edinburgh EH9 3JJ, UK.
Chem Soc Rev. 2012 Jun 7;41(11):4335-55. doi: 10.1039/c2cs35035a. Epub 2012 Apr 24.
The initial stages of drug discovery are increasingly reliant on development and improvement of analytical methods to investigate protein-protein and protein-ligand interactions. For over 20 years, mass spectrometry (MS) has been recognized as providing a fast, sensitive and high-throughput methodology for analysis of weak non-covalent complexes. Careful control of electrospray ionization conditions has enabled investigation of the structure, stability and interactions of proteins and peptides in a solvent free environment. This critical review covers the use of mass spectrometry for kinetic, dynamic and structural studies of proteins and protein complexes. We discuss how conjunction of mass spectrometry with related techniques and methodologies such as ion mobility, hydrogen-deuterium exchange (HDX), protein footprinting or chemical cross-linking can provide us with structural information useful for drug development. Along with other biophysical techniques, such as NMR or X-ray crystallography, mass spectrometry provides a powerful toolbox for investigation of biological problems of medical relevance (204 references).
药物发现的初始阶段越来越依赖于分析方法的开发和改进,以研究蛋白质-蛋白质和蛋白质-配体相互作用。20 多年来,质谱(MS)已被公认为是一种快速、灵敏和高通量的方法,可用于分析弱非共价复合物。对电喷雾电离条件的仔细控制,使我们能够在无溶剂环境中研究蛋白质和肽的结构、稳定性和相互作用。这篇综述涵盖了质谱在蛋白质和蛋白质复合物的动力学、动态和结构研究中的应用。我们讨论了如何将质谱与相关技术和方法(如离子淌度、氢-氘交换(HDX)、蛋白质足迹或化学交联)结合使用,为药物开发提供有用的结构信息。与其他生物物理技术(如 NMR 或 X 射线晶体学)一样,质谱为研究具有医学相关性的生物学问题提供了一个强大的工具箱(204 篇参考文献)。