化学
质谱法
寡肽酶
配体(生物化学)
离子迁移光谱法
分子
分子动力学
立体化学
计算化学
生物物理学
色谱法
生物化学
有机化学
酶
受体
生物
作者
Roos Van Elzen,Albert Konijnenberg,Pieter Van der Veken,Matthew Edgeworth,James H. Scrivens,Vilmos Fülöp,Frank Sobott,Anne‐Marie Lambeir
标识
DOI:10.1021/acs.jmedchem.4c00866
摘要
Ion mobility mass spectrometry (IM-MS) can be used to analyze native proteins according to their size and shape. By sampling individual molecules, it allows us to study mixtures of conformations, as long as they have different collision cross sections and maintain their native conformation after dehydration and vaporization in the mass spectrometer. Even though conformational heterogeneity of prolyl oligopeptidase has been demonstrated in solution, it is not detectable in IM-MS. Factors that affect the conformation in solution, binding of an active site ligand, the stabilizing Ser554Ala mutation, and acidification do not qualitatively affect the collision-induced unfolding pattern. However, measuring the protection of accessible cysteines upon ligand binding provides a principle for the development of MS-based ligand screening methods.
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