用交联质谱法填补蛋白质结构生物学中缺失的拼图。

Q3 Biochemistry, Genetics and Molecular Biology
QRB Discovery Pub Date : 2024-12-27 eCollection Date: 2025-01-01 DOI:10.1017/qrd.2024.13
Zheng Ser
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引用次数: 0

摘要

蛋白质复合体的高分辨率结构提供了丰富的蛋白质结构和功能信息。这些蛋白质结构的数据库也用于基于人工智能(AI)的结构建模方法。尽管结构生物学家已经确定了丰富的蛋白质结构,但在蛋白质结构生物学的拼图中仍然存在空白或缺失的部分。蛋白质结构中可能缺少高度灵活的区域,现有数据库可能无法捕获不同蛋白质复合体状态的构象变化。从这个角度来看,我概述了交联质谱法可以帮助填补这些缺失部分的几种方法:鉴定其他结构技术无法捕获的高度柔性蛋白质区域中的交联相互作用;捕捉蛋白质复合物在不同功能状态下的构象变化;在综合结构建模中作为距离约束,提供蛋白质的结构信息。交联质谱法在结构生物学中填补缺失部分的无数方式使其成为结构生物学中强大的技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Filling in missing puzzle pieces in protein structural biology with cross-linking mass spectrometry.

High resolution structures of protein complexes provide a wealth of information on protein structure and function. Databases of these protein structures are also used for artificial-intelligence (AI)-based methods of structural modelling. Despite the wealth of protein structures that have been determined by structural biologists, there are still gaps, or missing pieces in the puzzle of protein structural biology. Highly flexible regions may be missing from protein structures and conformational changes of different protein complex states may not be captured by current databases. In this perspective, I sketch out several ways that cross-linking mass spectrometry can contribute to filling in some of these missing pieces: Identification of cross-linked interactions in highly flexible protein regions not captured by other structural techniques; capturing conformational changes of protein complexes in different functional states; serving as distance constraints in integrative structural modelling and providing structural information of in cellulo proteins. The myriad ways in which cross-linking mass spectrometry contributes to filling in missing pieces in structural biology makes it a powerful technique in structural biology.

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来源期刊
QRB Discovery
QRB Discovery Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
3.60
自引率
0.00%
发文量
18
审稿时长
12 weeks
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