Institute of Molecular Biology, National Chung Hsing University, Taichung, Taiwan.
Anal Bioanal Chem. 2011 Sep;401(4):1219-29. doi: 10.1007/s00216-011-5198-6. Epub 2011 Jul 5.
In this study, we developed a novel microwave-assisted protein preparation and digestion method for matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry analysis and identification of proteins that involves using conductive carbon tape as a sample platform for sample preparation (reduction and alkylation) and digestion under microwave heating and as a plate for MALDI analysis. This method allows for the enzymatic digestion products of proteins to be directly analyzed by MALDI mass spectrometry and results in a marked reduction in sample loss. Our protocol requires only a small volume (1 μL) of reaction solvent, which increases the frequency of enzyme-to-protein contact, thereby resulting in more efficient digestion of sample than conventional in-solution digestion methods. To test this protocol, we used magnetic iron (II, III) oxide nanoparticles as concentrating probes to enrich phosphopeptides from a mixture of peptides in enzymatically digested protein samples. We found that the one-pot on-tape-based protein preparation and digestion under microwave heating combined with the on-tape-based enrichment method not only dramatically reduced the time required for phosphopeptides analysis but also allowed for the simultaneous identification of phosphoproteins. The advantages of our protocol include ease of use, high digestion efficiency, high specificity, and rapid (15 min) identification of proteins and enrichment of phosphopeptides in a mixture of enzymatically digested protein samples.
在这项研究中,我们开发了一种新的微波辅助蛋白质制备和消化方法,用于基质辅助激光解吸/电离(MALDI)飞行时间质谱分析和蛋白质鉴定,该方法涉及使用导电碳带作为样品平台进行样品制备(还原和烷基化)和微波加热下的消化,以及 MALDI 分析的板。该方法允许直接通过 MALDI 质谱分析蛋白质的酶解产物,并且明显减少了样品损失。我们的方案仅需要 1 μL 的反应溶剂,这增加了酶与蛋白质的接触频率,从而导致比传统的溶液内消化方法更有效地消化样品。为了测试该方案,我们使用磁性铁(II,III)氧化物纳米粒子作为浓缩探针,从酶解蛋白质样品中混合的肽中富集磷酸肽。我们发现,微波加热下的基于一管的蛋白质制备和消化与基于一管的富集方法相结合,不仅大大缩短了磷酸肽分析所需的时间,而且还允许同时鉴定磷酸蛋白。我们方案的优点包括易于使用、高消化效率、高特异性以及快速(15 分钟)鉴定混合物中酶解蛋白质样品中的蛋白质和磷酸肽的富集。