首页> 外文期刊>Molecular & cellular proteomics: MCP >Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MS
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Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MS

机译:人血清白蛋白糖基化肽诊断片段离子文库的开发:通过并行反应监测,SWATH和MS在糖尿病前期,糖尿病和微量白蛋白尿血浆中的靶向定量

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摘要

Human serum albumin is one of the most abundant plasma proteins that readily undergoes glycation, thus glycated albumin has been suggested as an additional marker for monitoring glycemic status. Hitherto, only Amadori-modified peptides of albumin were quantified. In this study, we report the construction of fragment ion library for Amadori-modified lysine (AML), N(e)-(car-boxymethyl)lysine (CML)-, and N(e)-(carboxyethyl)lysine (CEL)-modified peptides of the corresponding synthetically modified albumin using high resolution accurate mass spectrometry (HR/AM). The glycated peptides were manually inspected and validated for their modification. Further, the fragment ion library was used for quantification of glycated peptides of albumin in the context of diabetes. Targeted Sequential Window Acquisition of all THeoretical Mass Spectra (SWATH) analysis in pooled plasma samples of control, prediabetes, diabetes, and microalbuminuria, has led to identification and quantification of 13 glycated peptides comprised of four AML, seven CML, and two CEL modifications, representing nine lysine sites of albumin. Five lysine sites namely K549, K438, K490, K88, and K375, were observed to be highly sensitive for glycation modification as their respective m/z showed maximum fold change and had both AML and CML modifications. Thus, peptides involving these lysine sites could be potential novel markers to assess the degree of glycation in diabetes. Diabetes is a complex metabolic disorder characterized by prolonged hyperglycemia resulting from defects in insulin secretion, insulin action, or both, leading to abnormalities in carbohydrate, fat, and protein metabolism (1). According to the projection by the International Diabetes Foundation, around 592 million people will be affected by diabetes by the year 2040 (2). Diabetes and its associated complications are becoming global public health problems and posing a serious challenge in disease management.
机译:人血清白蛋白是最容易发生糖基化的最丰富的血浆蛋白之一,因此糖基化白蛋白已被建议作为监测血糖状态的另一标记。迄今为止,仅对Amadori修饰的白蛋白肽进行了定量。在这项研究中,我们报告了Amadori修饰的赖氨酸(AML),N(e)-(羧甲基)赖氨酸(CML)-和N(e)-(羧乙基)赖氨酸(CEL)片段离子文库的构建高分辨率精确质谱法(HR / AM)对相应合成修饰的白蛋白的修饰肽进行修饰。手动检查糖基化肽并验证其修饰。此外,片段离子文库用于在糖尿病的情况下定量白蛋白的糖基化肽。在对照,糖尿病前期,糖尿病和微量白蛋白尿的合并血浆样本中,对所有理论质谱(SWATH)分析进行有针对性的顺序窗口采集,已导致鉴定和定量了13种糖化肽,包括4种AML,7种CML和2种CEL修饰,代表白蛋白的9个赖氨酸位点。观察到五个赖氨酸位点,即K549,K438,K490,K88和K375,对糖基化修饰高度敏感,因为它们各自的m / z显示最大倍数变化,并且同时具有AML和CML修饰。因此,涉及这些赖氨酸位点的肽可能是评估糖尿病中糖基化程度的潜在新标记。糖尿病是一种复杂的代谢紊乱,其特征是胰岛素分泌缺陷,胰岛素作用或两者兼而有之,导致高血糖时间延长,从而导致碳水化合物,脂肪和蛋白质代谢异常(1)。根据国际糖尿病基金会的预测,到2040年,大约5.92亿人将受到糖尿病的影响(2)。糖尿病及其相关并发症正在成为全球公共卫生问题,并在疾病管理方面提出了严峻的挑战。

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