Guo Hongbo, Peng Hui, Emili Andrew
a Donnelly Centre for Cellular and Biomolecular Research , University of Toronto , Toronto , ON , Canada.
b Department of Chemistry , University of Toronto , Toronto , ON , Canada.
Expert Opin Drug Discov. 2017 Dec;12(12):1271-1280. doi: 10.1080/17460441.2017.1378178. Epub 2017 Sep 21.
To understand and manipulate biochemical processes and signaling pathways, the knowledge of endogenous protein-metabolite interactions would be extremely helpful. Recent developments in precision mass spectrometry, high-throughput proteomics and sensitive metabolomic profiling are beginning to converge on a possible solution, heralding a new era of global metabolome-proteome 'interactome' studies that promise to change biomedical research and drug discovery. Areas covered: Here, we review innovative mass spectrometry-based methods and recent pioneering studies aimed at elucidating the physical associations of small molecule ligands with cellular proteins. The technologies covered belong to two main categories: tag-based and tag-free methods. We emphasize the latter in this review, and outline promising experimental workflows and key data analysis considerations involved. Expert opinion: Recent ground-breaking advances in chemical-proteomics technology and allied computational methods now make the global detection of protein-ligand engagement an increasingly attractive research problem. Despite ongoing challenges, rapid progress in the field is expected these coming next few years, leading to a refreshed systems biology research paradigm and much needed new opportunities for improving sparse drug discovery pipelines.
为了理解和操控生化过程及信号通路,了解内源性蛋白质-代谢物相互作用将极有帮助。精准质谱、高通量蛋白质组学和灵敏代谢组分析的最新进展开始汇聚成一种可能的解决方案,预示着全球代谢组-蛋白质组“相互作用组”研究的新时代,有望改变生物医学研究和药物发现。涵盖领域:在此,我们综述基于质谱的创新方法以及近期旨在阐明小分子配体与细胞蛋白质物理关联的开创性研究。所涵盖的技术主要分为两类:基于标签的方法和无标签方法。在本综述中我们重点介绍后者,并概述有前景的实验工作流程以及关键数据分析考量。专家观点:化学蛋白质组学技术及相关计算方法最近取得的突破性进展,如今使蛋白质-配体相互作用的全局检测成为一个越来越有吸引力的研究课题。尽管仍存在挑战,但预计未来几年该领域将取得快速进展,带来焕然一新的系统生物学研究范式以及改善稀疏药物发现流程急需的新机遇。