{"title":"Digestion, Purification, and Enrichment of Protein Samples for Mass Spectrometry","authors":"Victoria E. Hedrick, Mercedes N. LaLand, Ernesto S. Nakayasu, Lake N. Paul","doi":"10.1002/9780470559277.ch140272","DOIUrl":null,"url":null,"abstract":"<p>Proteomic studies rely heavily on the use of liquid chromatography (LC)–mass spectrometry (MS and MS/MS) analyses to provide information about protein composition and function. Profiling the proteome can be the first step to understanding biological pathways, but the challenges scientists face with the complex nature of proteins and proteolysis products can be daunting. Techniques involving fractionation, immunoprecipitation, and phosphopeptide enrichment can simplify complex protein mixtures and enhance the amount of target proteins that are important to the investigator. Emphasis on sample preparation for LC-MS/MS analyses is essential to acquisition of high-quality data for proteomic research. Certain classes of reagents, materials, and contaminants that can be introduced during sample processing may limit the effectiveness of LC-MS/MS analysis. These protocols outline methods for proteolytic digestion of proteins that are compatible with LC-MS/MS, along with procedures that allow for simplification of complex protein matrices. © 2015 by John Wiley & Sons, Inc.</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"7 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9780470559277.ch140272","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470559277.ch140272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 16
Abstract
Proteomic studies rely heavily on the use of liquid chromatography (LC)–mass spectrometry (MS and MS/MS) analyses to provide information about protein composition and function. Profiling the proteome can be the first step to understanding biological pathways, but the challenges scientists face with the complex nature of proteins and proteolysis products can be daunting. Techniques involving fractionation, immunoprecipitation, and phosphopeptide enrichment can simplify complex protein mixtures and enhance the amount of target proteins that are important to the investigator. Emphasis on sample preparation for LC-MS/MS analyses is essential to acquisition of high-quality data for proteomic research. Certain classes of reagents, materials, and contaminants that can be introduced during sample processing may limit the effectiveness of LC-MS/MS analysis. These protocols outline methods for proteolytic digestion of proteins that are compatible with LC-MS/MS, along with procedures that allow for simplification of complex protein matrices. © 2015 by John Wiley & Sons, Inc.
质谱分析中蛋白质样品的消化、纯化和富集
蛋白质组学研究在很大程度上依赖于使用液相色谱(LC) -质谱(MS和MS/MS)分析来提供有关蛋白质组成和功能的信息。分析蛋白质组可能是理解生物学途径的第一步,但科学家面临的蛋白质和蛋白质水解产物的复杂性质的挑战可能令人生畏。涉及分馏、免疫沉淀和磷酸肽富集的技术可以简化复杂的蛋白质混合物,并增加对研究者重要的目标蛋白质的数量。强调LC-MS/MS分析的样品制备对于获得蛋白质组学研究的高质量数据至关重要。样品处理过程中可能引入的某些类型的试剂、材料和污染物可能会限制LC-MS/MS分析的有效性。这些协议概述了与LC-MS/MS兼容的蛋白质水解消化方法,以及允许简化复杂蛋白质基质的程序。©2015 by John Wiley &儿子,Inc。
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