Ligand Modification-Free Methods for the Profiling of Protein-Environmental Chemical Interactions

IF 3.8 3区 医学 Q2 CHEMISTRY, MEDICINAL
Yanan Li, Jiawen Lyu, Yan Wang, Mingliang Ye* and Hailin Wang*, 
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Abstract

Adverse health outcomes caused by environmental chemicals are often initiated via their interactions with proteins. Essentially, one environmental chemical may interact with a number of proteins and/or a protein may interact with a multitude of environmental chemicals, forming an intricate interaction network. Omics-wide protein-environmental chemical interaction profiling (PECI) is of prominent importance for comprehensive understanding of these interaction networks, including the toxicity mechanisms of action (MoA), and for providing systematic chemical safety assessment. However, such information remains unknown for most environmental chemicals, partly due to their vast chemical diversity. In recent years, with the continuous efforts afforded, especially in mass spectrometry (MS) based omics technologies, several ligand modification-free methods have been developed, and new attention for systematic PECI profiling was gained. In this Review, we provide a comprehensive overview on these methodologies for the identification of ligand-protein interactions, including affinity interaction-based methods of affinity-driven purification, covalent modification profiling, and activity-based protein profiling (ABPP) in a competitive mode, physicochemical property changes assessment methods of ligand-directed nuclear magnetic resonance (ligand-directed NMR), MS integrated with equilibrium dialysis for the discovery of allostery systematically (MIDAS), thermal proteome profiling (TPP), limited proteolysis-coupled mass spectrometry (LiP-MS), stability of proteins from rates of oxidation (SPROX), and several intracellular downstream response characterization methods. We expect that the applications of these ligand modification-free technologies will drive a considerable increase in the number of PECI identified, facilitate unveiling the toxicological mechanisms, and ultimately contribute to systematic health risk assessment of environmental chemicals.

Abstract Image

Abstract Image

分析蛋白质与环境化学相互作用的无配体修饰方法。
环境化学物质造成的不良健康后果往往是通过它们与蛋白质的相互作用引起的。从本质上讲,一种环境化学物质可能与多种蛋白质相互作用,和/或一种蛋白质可能与多种环境化学物质相互作用,从而形成错综复杂的相互作用网络。全 Omics 蛋白质-环境化学相互作用分析(PECI)对于全面了解这些相互作用网络(包括毒性作用机制)以及提供系统的化学安全评估具有突出的重要意义。然而,对于大多数环境化学物质来说,这些信息仍然是未知的,部分原因是这些化学物质具有巨大的化学多样性。近年来,随着人们的不断努力,特别是基于质谱(MS)的全息技术的发展,已经开发出了几种无需配体修饰的方法,系统性的 PECI 图谱分析得到了新的关注。在本综述中,我们将全面综述这些用于鉴定配体-蛋白质相互作用的方法,包括基于亲和相互作用的亲和驱动纯化方法、共价修饰剖析和竞争模式下基于活性的蛋白质剖析(ABPP)、配体定向核磁共振(配体定向 NMR)的理化性质变化评估方法、质谱与平衡透析相结合系统发现异构体(MIDAS)、热蛋白质组分析(TPP)、有限蛋白质分解耦合质谱(LiP-MS)、从氧化率看蛋白质的稳定性(SPROX),以及多种细胞内下游反应表征方法。我们预计,这些无配体修饰技术的应用将大大增加已鉴定的 PECI 的数量,促进毒理学机制的揭示,并最终有助于对环境化学品进行系统的健康风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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