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Trace analysis of proteins using postseparation solution-phase digestion and electrospray mass spectrometric detection of marker peptides

机译:使用分离后溶液相消化和电喷雾质谱检测标记肽对蛋白质进行痕量分析

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摘要

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.
机译:蛋白质绝对定量的分析方法通常包括一个消化步骤,通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是在LC-MS分析系统之前实施的,需要高序列覆盖率才能进行明确的蛋白质鉴定。对于氨基酸序列具有强烈重叠的蛋白质(例如治疗性蛋白质及其代谢物),必须在消化之前进行蛋白质分离,然后对标记物肽进行电喷雾质谱分析。在这里,我们介绍了一种在线柱后溶液相消化方法,该方法基于连续注入纳米C18反相柱下游的蛋白水解酶胃蛋白酶。根据蛋白质的保留时间,结合检测柱后消化物中形成的特定标记肽来鉴定蛋白质。描述了重要参数的优化,例如酶浓度,反应时间和有机改性剂浓度。我们证明了连续流溶液相消化方法可以在线耦合到蛋白质的反相梯度液相色谱分离。获得的五种模型蛋白的检出限为30/90 fmol,m / z值为300-1000,是特异的标记肽,线性响应高达3 pmol。

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