Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, Oxford OX1 3QZ, UK.
Curr Opin Struct Biol. 2011 Oct;21(5):641-9. doi: 10.1016/j.sbi.2011.08.002. Epub 2011 Aug 29.
Over the past two decades, mass spectrometry (MS) has emerged as a bone fide approach for structural biology. MS can inform on all levels of protein organization, and enables quantitative assessments of their intrinsic dynamics. The key advantages of MS are that it is a sensitive, high-resolution separation technique with wide applicability, and thereby allows the interrogation of transient protein assemblies in the context of complex mixtures. Here we describe how molecular-level information is derived from MS experiments, and how it can be combined with spatial and dynamical restraints obtained from other structural biology approaches to allow hybrid studies of protein architecture and movements.
在过去的二十年中,质谱(MS)已成为结构生物学的一种可靠方法。MS 可以提供蛋白质组织的各个层面的信息,并能够对其内在动力学进行定量评估。MS 的主要优势在于它是一种灵敏、高分辨率的分离技术,具有广泛的适用性,因此可以在复杂混合物的背景下研究瞬时蛋白质组装。在这里,我们描述了如何从 MS 实验中得出分子水平的信息,以及如何将其与来自其他结构生物学方法的空间和动力学约束相结合,以允许对蛋白质结构和运动进行混合研究。