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寡糖的碰撞诱导碎片化:基于质谱的糖组学的机理见解

Collision-Induced Fragmentation of Oligosaccharides: Mechanistic Insights for Mass Spectrometry-Based Glycomics.

作者信息

Geue Niklas, Safferthal Marc, Pagel Kevin

机构信息

Institute of Chemistry and Biochemistry, Freie Universität Berlin, Altensteinstraße 23a, 14195, Berlin, Germany.

Department of Molecular Physics, Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, 14195, Berlin, Germany.

出版信息

Angew Chem Int Ed Engl. 2025 Aug 11;64(33):e202511591. doi: 10.1002/anie.202511591. Epub 2025 Jul 21.

DOI:10.1002/anie.202511591
PMID:40631944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12338385/
Abstract

Structural alterations in oligosaccharides are often associated with disease, positioning clinical glycomics as an emerging tool for diagnostics. This is most commonly achieved using a controlled collision-induced dissociation (CID) of larger oligosaccharides into fragments and measuring their mass in a mass spectrometer. Due to the complexity of oligosaccharides, and particularly their unusual fragmentation mechanisms, the underlying processes are poorly understood. Deciphering glycan fragmentation and making it understandable is highly desirable and would transform the field of glycomics from an expert technique into a widely applicable tool available to non-specialists. Here, we review the current knowledge of glycan fragmentation mechanisms in CID, with particular emphasis on hexose migrations and the anomeric memory. We discuss challenges and perspectives for future investigations, opening the window to widespread use of glycomics in clinical applications based on a fundamental understanding of glycan fragmentation.

摘要

寡糖的结构改变常与疾病相关,这使得临床糖组学成为一种新兴的诊断工具。这通常是通过将较大的寡糖进行可控的碰撞诱导解离(CID)成片段,并在质谱仪中测量其质量来实现的。由于寡糖的复杂性,尤其是其不寻常的碎片化机制,其潜在过程尚不清楚。破解聚糖碎片化并使其易于理解是非常必要的,这将把糖组学领域从一种专家技术转变为非专业人员也可广泛使用的工具。在这里,我们回顾了CID中聚糖碎片化机制的当前知识,特别强调己糖迁移和异头碳记忆。我们讨论了未来研究的挑战和前景,基于对聚糖碎片化的基本理解,为糖组学在临床应用中的广泛使用打开了窗口。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/2b4fba205ba7/ANIE-64-e202511591-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/d3b00d418ecf/ANIE-64-e202511591-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/ebe6387ac74d/ANIE-64-e202511591-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/47a41672a2a7/ANIE-64-e202511591-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/334c30e839d4/ANIE-64-e202511591-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/1b65eee136c2/ANIE-64-e202511591-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/6eaed12ee88a/ANIE-64-e202511591-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/3055f5af8afe/ANIE-64-e202511591-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/2b4fba205ba7/ANIE-64-e202511591-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/d3b00d418ecf/ANIE-64-e202511591-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/ebe6387ac74d/ANIE-64-e202511591-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/47a41672a2a7/ANIE-64-e202511591-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/334c30e839d4/ANIE-64-e202511591-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/1b65eee136c2/ANIE-64-e202511591-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/6eaed12ee88a/ANIE-64-e202511591-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/3055f5af8afe/ANIE-64-e202511591-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1669/12338385/2b4fba205ba7/ANIE-64-e202511591-g011.jpg

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