利用亲水富集策略分析人血浆中N-糖基化蛋白及N-糖类型 = Analysis of N-glycosylated protein and N-glycans in human plasma by hydrophilic enrichment strategy

蛋白质的N- 糖基化是最重要的翻译后修饰之一, 许多已知的血浆肿瘤诊断标志物及治疗靶标都是N- 糖基化 蛋白。 针对血浆的糖蛋白质组研究有利于发现新的蛋白标志物。然而,血浆蛋白质浓度分布的动态范围非常宽,且同一位点上的糖链存在微观不均一性,影响了血浆中糖蛋白的鉴定效率。本文利用亲水材料ZIC-HILIC制备亲 水富集柱分别对人血浆中的N- 糖链和N- 糖肽进行富集,并结合碱性反相色谱进行肽段的预分离和高准确度质谱 分析,最终在健康人的血浆中鉴定到了 299 个糖基化蛋白、637 个糖基化位点,并识别出 31 种不同的糖型。在这些 鉴定到的糖基化位点中,新发现有 107 个 N- 糖基化位点(占...

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Main Authors: 马成 Ma, Cheng, 潘一廷 Pan, Yiting, 张琪 Zhang, Qi, 王继峰 Wang, Jifeng, 钱小红 Qian, Xiaohong, 应万涛 Ying, Wantao
Other Authors: School of Biological Sciences
Format: Article
Language:Chinese
Published: 2015
Subjects:
Online Access:https://hdl.handle.net/10356/106581
http://hdl.handle.net/10220/25055
http://www.chrom-china.com/EN/abstract/abstract13508.shtml
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Institution: Nanyang Technological University
Language: Chinese
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Summary:蛋白质的N- 糖基化是最重要的翻译后修饰之一, 许多已知的血浆肿瘤诊断标志物及治疗靶标都是N- 糖基化 蛋白。 针对血浆的糖蛋白质组研究有利于发现新的蛋白标志物。然而,血浆蛋白质浓度分布的动态范围非常宽,且同一位点上的糖链存在微观不均一性,影响了血浆中糖蛋白的鉴定效率。本文利用亲水材料ZIC-HILIC制备亲 水富集柱分别对人血浆中的N- 糖链和N- 糖肽进行富集,并结合碱性反相色谱进行肽段的预分离和高准确度质谱 分析,最终在健康人的血浆中鉴定到了 299 个糖基化蛋白、637 个糖基化位点,并识别出 31 种不同的糖型。在这些 鉴定到的糖基化位点中,新发现有 107 个 N- 糖基化位点(占总位点数的 16.8%)。 本方法操作简单,可以有效富集N- 糖肽和 N- 糖,为在血浆中寻找糖蛋白和糖链生物标志物提供了可靠的手段。N-glycosylation of proteins is one of the most important post-translational modifications (PTM). Many diagnostic biomarkers and therapeutic targets are glycosylated proteins. However, it is still a big challenge to identify glycoproteins in human plasma, because of the high dynamic range and microheterogeneity of glycosylation. In this work, hydrophilic interaction liquid chromatography (HILIC) enrichment, high-pH reversed-phase prefractionation and high accurate mass spectrometry (MS) analysis were combined to profile the N-glycoproteins in human plasma. In total, 637 N-glycosites from 299 glycoproteins (protein groups) were identified. There were also 31 glycoforms recognized after HILIC enrichment and MS analysis. Among the results, 107 glycosylation sites (16.8%) are newly found. This study provided a simple and reliable strategy for exploring potential N-glycoprotein biomarkers from complicated biological systems.