Alyson P. Black, P. Angel, Richard R Drake, A. Mehta
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{"title":"Antibody Panel Based N‐Glycan Imaging for N‐Glycoprotein Biomarker Discovery","authors":"Alyson P. Black, P. Angel, Richard R Drake, A. Mehta","doi":"10.1002/cpps.99","DOIUrl":null,"url":null,"abstract":"Antibody panel based N‐glycan imaging is a novel platform for N‐glycan analysis of immunocaptured proteins. N‐glycosylation is a post‐translational modification of pathophysiological importance and is often studied in the context of disease biomarkers. Determination of protein‐specific N‐glycosylation changes in patient samples has traditionally been laborious or limited to study of a single protein per analysis. This novel technique allows for the multiplexed analysis of N‐glycoproteins from biofluids. Briefly, this platform consists of antibodies spotted in an array panel to a microscope slide, specific capture of glycoproteins from a biological sample, and then enzymatic release of N‐glycans for analysis by matrix‐assisted laser desorption/ionization (MALDI) mass spectrometry (MS). N‐glycans are detected at each individual spot, allowing N‐glycan information to easily be linked back to its protein carrier. Using this protocol, multiplexed analysis of N‐glycosylation on serum glycoproteins can be performed. Human serum is discussed here, but this method has potential to be applied to other biofluids and to any glycoprotein that can be captured by a validated antibody. © 2019 by John Wiley & Sons, Inc.","PeriodicalId":10866,"journal":{"name":"Current Protocols in Protein Science","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpps.99","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Protein Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpps.99","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 15
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基于抗体面板的N -糖蛋白成像用于发现N -糖蛋白生物标志物
基于抗体面板的N‐聚糖成像是一种用于免疫捕获蛋白N‐聚糖分析的新平台。N-糖基化是一种具有病理生理重要性的翻译后修饰,通常在疾病生物标志物的背景下进行研究。传统上,患者样本中蛋白质特异性N-糖基化变化的测定是费力的,或者仅限于每次分析单个蛋白质的研究。这项新技术允许对生物流体中的N-糖蛋白进行多重分析。简言之,该平台由在显微镜载玻片的阵列面板中发现的抗体、从生物样品中特异性捕获糖蛋白,然后酶促释放N-聚糖以通过基质辅助激光解吸/电离(MALDI)质谱(MS)进行分析组成。在每个单独的位点检测到N‐聚糖,使N‐聚糖信息能够很容易地连接回其蛋白质载体。使用该方案,可以对血清糖蛋白上的N-糖基化进行多重分析。这里讨论了人类血清,但这种方法有可能应用于其他生物流体和任何可以被验证抗体捕获的糖蛋白。©2019 John Wiley&Sons,股份有限公司版权所有。
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