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Peptide and Protein Quantitation by Acid-Catalyzed ~(18)O-Labeling of Carboxyl Groups

机译:酸催化〜(18)O-标记羧基的肽和蛋白质定量

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We have developed a new method that applies acidic catalysis with hydrochloric acid for ~(18)O-labeling of peptides at their carboxyl groups. With this method, peptides get labeled at their C-terminus, at Asp and Glu residues, and at carboxymethyl-ated cysteine residues. Oxygen atoms at phosphate groups of phosphopeptide are not exchanged. Our elaborated labeling protocol is easy to perform, fast (5 h and 30 min), and results in 95-97 atom percent incorporation of ~(18)O at carboxyl groups. Undesired side reactions, such as deamidation or peptide hydrolysis, occur only at a very low level under the conditions applied. In addition, data analysis can be performed automatically using common software tools, such as Mascot Distiller. We have demonstrated the capability of this method for the quantitation of peptides as well as for phosphopeptides.
机译:我们已经开发了一种新的方法,该方法使用盐酸进行酸性催化,可对肽的羧基进行〜(18)O标记。使用这种方法,肽段的C末端,Asp和Glu残基以及羧甲基化的半胱氨酸残基处都被标记。磷酸肽磷酸基团上的氧原子不交换。我们精心设计的标记方案易于执行,快速(5小时和30分钟),可导致〜(18)O在羧基上掺入95-97原子百分比。在所应用的条件下,不良反应(例如脱酰胺或肽水解)仅在非常低的水平上发生。此外,可以使用常见的软件工具(例如Mascot Distiller)自动执行数据分析。我们已经证明了这种方法对肽以及磷酸肽定量的能力。

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