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使用紫外光解进行蛋白质结构的自上而下的氢氘交换分析。

Top-Down Hydrogen-Deuterium Exchange Analysis of Protein Structures Using Ultraviolet Photodissociation.

机构信息

University of Victoria -Genome British Columbia Proteomics Centre , No. 3101-4464 Markham Street, Vancouver Island Technology Park , Victoria , British Columbia V8Z 7X8 , Canada.

Thermo Fisher Scientific , 355 River Oaks Parkway , San Jose , California 95134 , United States.

出版信息

Anal Chem. 2018 Mar 6;90(5):3079-3082. doi: 10.1021/acs.analchem.7b03655. Epub 2018 Feb 1.

DOI:10.1021/acs.analchem.7b03655
PMID:29336549
Abstract

Top-down hydrogen-deuterium exchange (HDX) analysis using electron capture or transfer dissociation Fourier transform mass spectrometry (FTMS) is a powerful method for the analysis of secondary structure of proteins in solution. The resolution of the method is a function of the degree of fragmentation of backbone bonds in the proteins. While fragmentation is usually extensive near the N- and C-termini, electron capture (ECD) or electron transfer dissociation (ETD) fragmentation methods sometimes lack good coverage of certain regions of the protein, most often in the middle of the sequence. Ultraviolet photodissociation (UVPD) is a recently developed fast-fragmentation technique, which provides extensive backbone fragmentation that can be complementary in sequence coverage to the aforementioned electron-based fragmentation techniques. Here, we explore the application of electrospray ionization (ESI)-UVPD FTMS on an Orbitrap Fusion Lumos Tribrid mass spectrometer to top-down HDX analysis of proteins. We have incorporated UVPD-specific fragment-ion types and fragment-ion mixtures into our isotopic envelope fitting software (HDX Match) for the top-down HDX analysis. We have shown that UVPD data is complementary to ETD, thus improving the overall resolution when used as a combined approach.

摘要

使用电子俘获或转移解离傅里叶变换质谱(FTMS)的自上而下的氢氘交换(HDX)分析是分析溶液中蛋白质二级结构的一种强大方法。该方法的分辨率是蛋白质中骨架键断裂程度的函数。虽然在 N 端和 C 端附近的断裂通常很广泛,但电子俘获(ECD)或电子转移解离(ETD)断裂方法有时会缺乏蛋白质某些区域的良好覆盖,通常是在序列的中间。紫外线光解(UVPD)是一种最近开发的快速断裂技术,它提供了广泛的骨架断裂,可以与上述基于电子的断裂技术在序列覆盖范围上互补。在这里,我们探索了将电喷雾电离(ESI)-UVPD FTMS 应用于轨道阱融合卢莫斯三重四极杆质谱仪,以进行蛋白质的自上而下的 HDX 分析。我们已经将 UVPD 特定的片段离子类型和片段离子混合物纳入我们的同位素包络拟合软件(HDX Match)中,用于自上而下的 HDX 分析。我们已经表明,UVPD 数据与 ETD 互补,因此当用作组合方法时,它可以提高整体分辨率。

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