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计算方法允许氢氘交换质谱在单个酰胺分辨率。

Computational method allowing Hydrogen-Deuterium Exchange Mass Spectrometry at single amide Resolution.

机构信息

Indiana University, Department of Informatics and Computing, Bloomington, IN, USA.

Philipps-University Marburg, Faculty of Chemistry & LOEWE Center for Synthetic Microbiology Hans-Meerwein-Strasse, 35043, Marburg, Germany.

出版信息

Sci Rep. 2017 Jun 19;7(1):3789. doi: 10.1038/s41598-017-03922-3.

Abstract

Hydrogen-deuterium exchange (HDX) coupled with mass spectrometry (HDXMS) is a rapid and effective method for localizing and determining protein stability and dynamics. Localization is routinely limited to a peptide resolution of 5 to 20 amino acid residues. HDXMS data can contain information beyond that needed for defining protein stability at single amide resolution. Here we present a method for extracting this information from an HDX dataset to generate a HDXMS protein stability fingerprint. High resolution (HR)-HDXMS was applied to the analysis of a model protein of a spectrin tandem repeat that exemplified an intuitive stability profile based on the linkage of two triple helical repeats connected by a helical linker. The fingerprint recapitulated expected stability maximums and minimums with interesting structural features that corroborate proposed mechanisms of spectrin flexibility and elasticity. HR-HDXMS provides the unprecedented ability to accurately assess protein stability at the resolution of a single amino acid. The determination of HDX stability fingerprints may be broadly applicable in many applications for understanding protein structure and function as well as protein ligand interactions.

摘要

氘氢交换(HDX)结合质谱(HDXMS)是一种快速有效的方法,用于定位和确定蛋白质的稳定性和动态。定位通常限于肽分辨率为 5 到 20 个氨基酸残基。HDXMS 数据可以包含超出单酰胺分辨率定义蛋白质稳定性所需的信息。在这里,我们提出了一种从 HDX 数据集提取信息的方法,以生成 HDXMS 蛋白质稳定性指纹。高分辨率(HR)-HDXMS 被应用于分析一个 spectrin 串联重复的模型蛋白,该蛋白的稳定性基于通过螺旋接头连接的两个三螺旋重复的连接呈现出直观的稳定性谱。指纹再现了预期的稳定性最大值和最小值,具有有趣的结构特征,证实了 spectrin 灵活性和弹性的拟议机制。HR-HDXMS 提供了在单个氨基酸分辨率下准确评估蛋白质稳定性的前所未有的能力。HDX 稳定性指纹的测定可能在许多应用中广泛适用于理解蛋白质结构和功能以及蛋白质配体相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/5476592/be5b849c9343/41598_2017_3922_Fig1_HTML.jpg

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