Department of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA.
Expert Rev Proteomics. 2012;9(1):47-58. doi: 10.1586/epr.11.75.
Ion mobility coupled to mass spectrometry has been an important tool in the fields of chemical physics and analytical chemistry for decades, but its potential for interrogating the structure of proteins and multiprotein complexes has only recently begun to be realized. Today, ion mobility-mass spectrometry is often applied to the structural elucidation of protein assemblies that have failed high-throughput crystallization or NMR spectroscopy screens. Here, we highlight the technology, approaches and data that have led to this dramatic shift in use, including emerging trends such as the integration of ion mobility-mass spectrometry data with more classical (e.g., 'bottom-up') proteomics approaches for the rapid structural characterization of protein networks.
几十年来,离子淌度与质谱联用一直是化学物理和分析化学领域的重要工具,但它在探测蛋白质和多蛋白复合物结构方面的潜力直到最近才开始被认识到。如今,离子淌度-质谱通常应用于那些未能通过高通量结晶或 NMR 光谱筛选的蛋白质组装体的结构阐明。在这里,我们重点介绍了导致这种用途的巨大转变的技术、方法和数据,包括一些新兴趋势,如将离子淌度-质谱数据与更经典的(例如“自上而下”)蛋白质组学方法相结合,用于快速蛋白质网络结构特征分析。