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氢氘交换质谱(HDX-MS)在药物发现中的概述。

An overview of hydrogen deuterium exchange mass spectrometry (HDX-MS) in drug discovery.

机构信息

a Protein and Nucleic Acid Chemistry Division , MRC Laboratory of Molecular Biology , Cambridge , UK.

b Department of Biochemistry and Microbiology , University of Victoria , Victoria , Canada.

出版信息

Expert Opin Drug Discov. 2017 Oct;12(10):981-994. doi: 10.1080/17460441.2017.1363734. Epub 2017 Aug 17.

Abstract

Hydrogen deuterium exchange mass spectrometry (HDX-MS) is a powerful methodology to study protein dynamics, protein folding, protein-protein interactions, and protein small molecule interactions. The development of novel methodologies and technical advancements in mass spectrometers has greatly expanded the accessibility and acceptance of this technique within both academia and industry. Areas covered: This review examines the theoretical basis of how amide exchange occurs, how different mass spectrometer approaches can be used for HDX-MS experiments, as well as the use of HDX-MS in drug development, specifically focusing on how HDX-MS is used to characterize bio-therapeutics, and its use in examining protein-protein and protein small molecule interactions. Expert opinion: HDX-MS has been widely accepted within the pharmaceutical industry for the characterization of bio-therapeutics as well as in the mapping of antibody drug epitopes. However, there is room for this technique to be more widely used in the drug discovery process. This is particularly true in the use of HDX-MS as a complement to other high-resolution structural approaches, as well as in the development of small molecule therapeutics that can target both active-site and allosteric binding sites.

摘要

氘氢交换质谱(HDX-MS)是一种强大的方法,用于研究蛋白质动力学、蛋白质折叠、蛋白质-蛋白质相互作用以及蛋白质与小分子相互作用。新方法的发展和质谱仪的技术进步极大地扩大了该技术在学术界和工业界的可及性和接受程度。涵盖领域:本文综述考察了酰胺交换发生的理论基础、不同的质谱仪方法如何用于 HDX-MS 实验,以及 HDX-MS 在药物开发中的应用,特别是侧重于 HDX-MS 如何用于表征生物治疗药物,以及其在研究蛋白质-蛋白质和蛋白质与小分子相互作用中的应用。专家意见:HDX-MS 在药物开发中已被制药行业广泛接受,用于生物治疗药物的表征以及抗体药物表位的作图。然而,该技术在药物发现过程中有更广泛应用的空间。这在将 HDX-MS 用作其他高分辨率结构方法的补充方面尤其如此,以及在开发可以靶向活性位点和变构结合位点的小分子治疗药物方面。

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