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用于寻找尿毒症毒素的质谱分析。

Mass spectrometry in the search for uremic toxins.

作者信息

Niwa T

机构信息

Nagoya University Daiko Medical Center, Japan.

出版信息

Mass Spectrom Rev. 1997 Nov-Dec;16(6):307-32. doi: 10.1002/(SICI)1098-2787(1997)16:6<307::AID-MAS1>3.0.CO;2-L.

Abstract

This article reviews the literature on the mass spectrometry (MS) that has been used in the research of uremic toxins. Gas chromatography/mass spectrometry (GC/MS) has been most often used for the analysis of low-molecular-weight compounds in uremic blood such as organic acids, phenols, and polyols. However, it cannot be used for the analysis of middle- to high-molecular-weight substances or for involatile compounds. The development of fast atom bombardment (FAB) and liquid secondary ion mass spectrometry (LSIMS) has made possible the analysis of middle-molecules and involatile low-molecular-weight substances such as peptides and nucleosides. The development of atmospheric pressure chemical ionization (APCI) has also lead to the analysis of involatile low-molecular-weight substances. The recent advances in ionization methods, such as electrospray ionization (ESI) and matrix-assisted laser desorption ionization (MALDI), have permitted the MS analysis of high-molecular-weight substances such as beta 2-microglobulin, a major component of dialysis amyloid. Liquid chromatography/mass spectrometry (LC/MS), using ESI, APCI, or FAB as an ionization method, is currently the preferred method for the analysis of low- to high-molecular-weight substances in uremic blood. ESI-LC/MS and matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOFMS) are useful for elucidating the structure of post-translationally modified proteins obtained from the blood and tissues of uremic patients. Post-translational modification such as the formation of advanced glycation end-products and carbamoylation is enhanced in uremic patients, and is considered to be responsible for some uremic symptoms. Laser microprobe MS is unique in its capability for the two-dimensional detection of atoms such as aluminum in a tissue section obtained from uremic patients. This review focuses on the mainstream research for discovering uremic toxins, specific uremic toxins identified or quantified using MS, and the MS analysis of post-translationally modified proteins in uremia. These studies have provided ample evidence that MS has played an important role in the search for uremic toxins.

摘要

本文综述了用于尿毒症毒素研究的质谱(MS)相关文献。气相色谱/质谱联用(GC/MS)最常用于分析尿毒症血液中的低分子量化合物,如有机酸、酚类和多元醇。然而,它不能用于分析中高分子量物质或难挥发化合物。快原子轰击(FAB)和液体二次离子质谱(LSIMS)的发展使得对中分子和难挥发的低分子量物质(如肽和核苷)的分析成为可能。大气压化学电离(APCI)的发展也使得对难挥发的低分子量物质的分析成为可能。电离方法的最新进展,如电喷雾电离(ESI)和基质辅助激光解吸电离(MALDI),使得对高分子量物质(如透析淀粉样变的主要成分β2-微球蛋白)进行质谱分析成为可能。液相色谱/质谱联用(LC/MS),以ESI、APCI或FAB作为电离方法,是目前分析尿毒症血液中低到高分子量物质的首选方法。ESI-LC/MS和基质辅助激光解吸电离飞行时间质谱(MALDI-TOFMS)有助于阐明从尿毒症患者血液和组织中获得的翻译后修饰蛋白质的结构。尿毒症患者中翻译后修饰(如晚期糖基化终产物的形成和氨基甲酰化)会增强,被认为是一些尿毒症症状的原因。激光微探针质谱在对尿毒症患者组织切片中的铝等原子进行二维检测方面具有独特能力。本综述重点关注发现尿毒症毒素的主流研究、使用质谱鉴定或定量的特定尿毒症毒素,以及尿毒症中翻译后修饰蛋白质的质谱分析。这些研究提供了充分的证据表明质谱在寻找尿毒症毒素方面发挥了重要作用。

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