Bruyneel B, Hoos J S, Smoluch M T, Lingeman H, Niessen W M A, Irth H
Vrije Universiteit Amsterdam, Faculty of Sciences, Department of Analytical Chemistry and Applied Spectroscopy, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.
Anal Chem. 2007 Feb 15;79(4):1591-8. doi: 10.1021/ac0616761.
Analytical methodologies for the absolute quantitation of proteins typically include a digest step often using trypsin as the proteolytic enzyme. In the majority of cases, off-line and on-line digestion methods are implemented prior to an LC-MS analysis system, requiring a high sequence coverage for unambiguous protein identification. For proteins with a strong overlap in amino acid sequence, e.g., therapeutic proteins and their metabolites, it is essential to separate proteins prior to digestion and the subsequent electrospray mass spectrometry analysis of marker peptides. Here, we present an on-line postcolumn solution-phase digestion methodology that is based on the continuous infusion of the proteolytic enzyme pepsin downstream to the nano C18 reversed-phase column. Proteins are identified based on their retention time in combination with the detection of specific marker peptides formed in the postcolumn digest. The optimization of important parameters such as enzyme concentration, reaction time, and organic modifier concentration is described. We demonstrated that the continuous-flow solution-phase digest method can be coupled on-line to the reversed-phase gradient liquid chromatography separation of proteins. Detection limits obtained for five model proteins, detected as specific marker peptides with m/z values of 300-1000, range from 30 to 90 fmol, with a linear response up to 3 pmol.
蛋白质绝对定量的分析方法通常包括一个消化步骤,该步骤常常使用胰蛋白酶作为蛋白水解酶。在大多数情况下,离线和在线消化方法在液相色谱 - 质谱分析系统之前实施,需要高序列覆盖率以明确鉴定蛋白质。对于氨基酸序列有强烈重叠的蛋白质,例如治疗性蛋白质及其代谢物,在消化以及随后对标记肽进行电喷雾质谱分析之前分离蛋白质至关重要。在此,我们提出一种在线柱后溶液相消化方法,该方法基于在纳米C18反相柱下游连续注入蛋白水解酶胃蛋白酶。基于蛋白质的保留时间并结合柱后消化中形成的特定标记肽的检测来鉴定蛋白质。描述了诸如酶浓度、反应时间和有机改性剂浓度等重要参数的优化。我们证明连续流溶液相消化方法可以在线连接到蛋白质的反相梯度液相色谱分离。以m/z值为300 - 1000检测为特定标记肽的五种模型蛋白质的检测限为30至90 fmol,线性响应高达3 pmol。