The Rosalind Franklin Institute, Harwell Campus, Didcot OX11 0FA, U.K.
Faculty of Medicine, Department of Metabolism, Digestion and Reproduction, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.
Anal Chem. 2024 Nov 12;96(45):17969-17977. doi: 10.1021/acs.analchem.4c02706. Epub 2024 Oct 30.
Previously, spatially resolved analysis of glycosaminoglycans (GAGs), by type and sulfation state, was unobtainable. Here, we describe a mass spectrometry imaging (MSI) approach which enables the detection, identification, localization, and profiling of GAG oligosaccharides directly from retinal tissue. Through treatment of tissues with relevant chondroitinase enzymes, we liberate and spatially resolve chondroitin, dermatan, and hyaluronan from disaccharides through to hexasaccharides, directly from tissue sections. We demonstrate the separation of isomeric GAG oligosaccharide ions at different histologically relevant regions using trapped ion mobility spectrometry (TIMS). This paper describes the first spatially resolved analysis of multiple GAGs and their oligosaccharide sulfation state(s) directly from tissues.
此前,糖胺聚糖(GAGs)的类型和硫酸化状态的空间分辨分析是无法实现的。在这里,我们描述了一种质谱成像(MSI)方法,该方法能够直接从视网膜组织中检测、识别、定位和分析 GAG 低聚糖。通过用相关的软骨素酶处理组织,我们从组织切片中直接将软骨素、真皮素和透明质酸从二糖释放并进行空间分辨,直至六糖。我们使用离子阱淌度质谱(TIMS)证明了在不同组织学相关区域分离异构 GAG 低聚糖离子的能力。本文描述了首次直接从组织中对多种 GAG 及其低聚糖硫酸化状态进行空间分辨分析。