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Enhanced Protein Identification using Graphite-Modified MALDI Plates for Offline LC-MALDI-MS/MS Bottom-up Proteomics

机译:使用石墨修饰的MALDI板增强的蛋白质鉴定用于离线LC-MALDI-MS / MS自下而上的蛋白质组学

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摘要

The use of offline liquid chromatography-matrix assisted laser desorption/ionization (LC-MALDI) tandem mass spectrometry (MS/MS) for bottom-up proteomics offers advantages in terms of cost, ease of use, and the time-decoupled nature of the separation step and the mass analysis. A method was developed to improve the capabilities of LC-MALDI-MS/MS in terms of protein identification in a bottom-up proteomic workflow. Enhanced protein identification is achieved by an increase in the MALDI signal intensity of the precursor peptides brought about by coating the MALDI plate with a thin film of graphite powder. Using the Escherichia coli proteome, it is demonstrated that the graphite-modified MALDI plates used in an offline LC-MALDI-MS/MS bottom-up protocol led to a 50 to 135% increase in the number of peptide identifications, and a concomitant 21% to 105% increase in the number of proteins inferred. We identify factors that lead to improvements in peptide sequence identifications and in the number of unique proteins identified when compared to using an unmodified MALDI plate. These improvements are achieved using a low cost approach that it is easy to implement, requires no major hardware/protocol modification, compatible with LC and adds no additional analysis time.
机译:使用离线液相色谱-基质辅助激光解吸/电离(LC-MALDI)串联质谱(MS / MS)进行自下而上的蛋白质组学在成本,易用性和时间分离性方面均具有优势分离步骤和质量分析。在自下而上的蛋白质组学工作流程中,开发了一种方法来提高LC-MALDI-MS / MS在蛋白质鉴定方面的能力。通过增加前体肽的MALDI信号强度来实现增强的蛋白质鉴定,该前体肽是通过用石墨粉末薄膜覆盖MALDI板而实现的。使用大肠埃希氏菌蛋白质组,证明了离线LC-MALDI-MS / MS自下而上方案中使用的石墨修饰的MALDI板导致肽段鉴定数量增加了50%至135%,并伴随着21 %到105%的推断蛋白质数量增加。当使用未修饰的MALDI板进行比较时,我们确定了导致肽序列鉴定和鉴定的独特蛋白质数量增加的因素。这些改进是使用易于实现的低成本方法实现的,不需要重大的硬件/协议修改,与LC兼容,并且不增加额外的分析时间。

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