Zheng Qiuling, Zhang Hao, Chen Hao
Center for Intelligent Chemical Instrumentation, Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701, USA.
Department of Chemistry, Washington University, St. Louis, MO 63130, USA.
Int J Mass Spectrom. 2013 Nov 1;353:84-92. doi: 10.1016/j.ijms.2013.04.009.
Bottom-up structural analysis of disulfide-bond containing proteins usually involves time-consuming offline enzymatic digestion, chemical reduction and thiol protection prior to mass spectrometric detection, which takes many hours. This paper presents an expedited bottom-up approach, employing desorption electrospray ionization-mass spectrometry (DESI-MS) coupled with online pepsin digestion and online electrochemical reduction of disulfide bonds. Peptides are generated in high digestion yield as its precursor protein in acidic aqueous solution flows through a pepsin column, which can undergo direct electrolysis. The electrolytic behaviors of peptides, as online monitored by DESI-MS, suggest the presence or absence of disulfide bonds in the peptides, and also provide information to relate disulfide bond-containing peptide precursors to their corresponding reduced products. Furthermore, selective electrolysis simply using different reduction potentials can be adopted to generate either partially or fully reduced peptides to assist disulfide bond mapping. In addition, it turns out that DESI is suitable for ionizing peptides in water without organic solvent additives (organic solvent additives would not be compatible with the use of pepsin column). The feasibility of this method was demonstrated using insulin, a protein carrying three pairs of disulfide-bonds as an example, in which all disulfide bond linkages and most of the protein sequence were successfully determined. Strikingly, this method shortens the sample digestion, reduction and MS detection from hours to less than 7 min, which could be of high value in high-throughput proteomics research.
对含二硫键的蛋白质进行自下而上的结构分析通常需要在质谱检测之前进行耗时的离线酶解、化学还原和硫醇保护,这需要数小时。本文介绍了一种加快的自下而上的方法,该方法采用解吸电喷雾电离质谱法(DESI-MS),结合在线胃蛋白酶消化和二硫键的在线电化学还原。当酸性水溶液中的前体蛋白质流经胃蛋白酶柱时,可直接进行电解,从而以高消化产率生成肽段。通过DESI-MS在线监测肽段的电解行为,可表明肽段中是否存在二硫键,还能提供信息将含二硫键的肽段前体与其相应的还原产物相关联。此外,只需采用不同的还原电位进行选择性电解,就可以生成部分或完全还原的肽段,以辅助二硫键图谱分析。另外,事实证明DESI适用于在不添加有机溶剂添加剂的水中电离肽段(有机溶剂添加剂与胃蛋白酶柱的使用不兼容)。以携带三对二硫键的蛋白质胰岛素为例,证明了该方法的可行性,其中成功确定了所有二硫键连接和大部分蛋白质序列。令人惊讶的是,该方法将样品消化、还原和质谱检测时间从数小时缩短至不到7分钟,这在高通量蛋白质组学研究中可能具有很高的价值。