Anal Chem. 2010 Feb 15;82(4):1171-4. doi: 10.1021/ac902477u.
The rapid and complete digestion of proteins is important when protein characterization by hydrogen-deuterium exchange (HDX) is coupled with mass spectrometry. We developed a single-pump, online, high-pressure digestion system that relies on UPLC technology to aid in the digestion of proteins. Two model proteins, amyloid beta-peptide 1-42 (Abeta 1-42) and an HIV-1 capsid mutant protein (NBSA), were used to demonstrate the efficacy of the high-pressure system. Both model proteins readily aggregate and are difficult to digest under normal conditions. Our high-pressure system successfully digests these proteins into small, overlapping peptides. The extra information afforded by overlapping peptides allows us to pinpoint HDX protection to protein segments smaller than the digested peptide. The calculated average segment length (ASL) for both model proteins decreased by 2-fold for high-pressure digestion compared to digestion at ambient pressure.
当氢氘交换(HDX)与质谱联用进行蛋白质特性分析时,蛋白质的快速完全消化非常重要。我们开发了一种单泵、在线、高压消化系统,该系统依赖于 UPLC 技术来辅助蛋白质消化。两种模型蛋白,淀粉样β肽 1-42(Abeta 1-42)和 HIV-1 衣壳突变蛋白(NBSA),被用于证明高压系统的功效。这两种模型蛋白都容易聚集,在正常条件下难以消化。我们的高压系统成功地将这些蛋白质消化成小的重叠肽。重叠肽提供的额外信息使我们能够将 HDX 保护精确定位到小于消化肽的蛋白质片段。与常压消化相比,两种模型蛋白的计算平均片段长度(ASL)在高压消化时降低了 2 倍。