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Complementary Protein and Peptide OFFGEL Fractionation for High-Throughput Proteomic Analysis

机译:互补蛋白质和肽OFFGEL分离用于高通量蛋白质组学分析

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OFFGEL fractionation of mouse kidney protein lysate and its tryptic peptide digest has been examined in this study for better understanding the differences between protein and peptide fractionation methods and attaining maximum recruitment of this modern methodology for in-depth proteomic analysis. With the same initial protein/peptide load for both fractionation methods, protein OFFGEL fractionation showed a preponderance in terms of protein identification, fractionation efficiency, and focusing resolution, while peptide OFF GEL was better in recovery, number of peptide matches, and protein coverage. This result suggests that the protein fractionation method is more suitable for shotgun analysis while peptide fractionation suits well quantitative peptide analysis [isobaric tags for relative and absolute quantitation (iTRAQ) or tandem mass tags (TMT)]. Taken together, utilization of the advantages of both fractionation approaches could be attained by coupling both methods to be applied on complex biological tissue. A typical result is shown in this article by identification of 8262 confident proteins of whole mouse kidney under stringent condition. We therefore fractionation as an effective and efficient addition to both label-free and quantitative label proteomics workflow.
机译:为了更好地理解蛋白质和多肽分级分离方法之间的差异,并最大程度地利用这种现代方法进行深入的蛋白质组学分析,本研究对小鼠肾脏蛋白质裂解物及其胰蛋白酶消化肽的OFFGEL分级进行了研究。在两种分离方法中,相同的初始蛋白质/肽上样量,蛋白质OFFGEL分离在蛋白质鉴定,分离效率和聚焦分辨率方面显示出优势,而肽OFF GEL在回收率,肽匹配数和蛋白质覆盖率方面更好。该结果表明蛋白质分级分离方法更适合于shot弹枪分析,而肽分级分离则适合定量肽分析[相对和绝对定量的等压标记(iTRAQ)或串联质量标记(TMT)]。两者合计,可以通过将两种方法结合应用在复杂的生物组织上来实现两种分离方法的优势。通过在严格条件下鉴定整个小鼠肾脏的8262个可信蛋白,可以显示出典型的结果。因此,我们将分级分离作为无标签和定量标签蛋白质组学工作流程的有效补充。

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