Chatterjee Sayantani, Zaia Joseph, Sethi Manveen K
Department of Biochemistry, Center for Biomedical Mass Spectrometry, Boston University School of Medicine, Boston, MA, USA.
Boston University Bioinformatics Program, Boston University, Boston, MA, USA.
Methods Mol Biol. 2025;2884:279-303. doi: 10.1007/978-1-0716-4298-6_18.
Mass spectrometry-based investigation of the heterogeneous glycoproteome from complex biological specimens is a robust approach to mapping the structure, function, and dynamics of the glycome and proteome. Sampling whole wet tissues often provides a large amount of starting material; however, there is a reasonable variability in tissue handling prior to downstream processing steps, and it is difficult to capture all the different biomolecules from a specific region. The on-slide tissue digestion approach, outlined in this protocol chapter, is a simple and cost-effective method that allows comprehensive mapping of the glycoproteome from a single spot of tissue of 1 mm or greater diameter. It provides a selection of target areas on tissue slides appropriate for tissue volumes of 10 nL or greater, corresponding to a 1 μL droplet of enzyme solution applied to a 1-mm diameter target on a 10-μm-thick tissue slice. Sequential enzymatic digestions and desalting of the biomolecules without any prior derivatization from the surface of fresh frozen or formalin-fixed paraffin-embedded tissue slides enable the simultaneous identification of glycosaminoglycan disaccharides such as hyaluronan, chondroitin sulfate and heparan sulfate, asparagine or N-linked glycans, and intact (glyco)peptides using liquid chromatography-tandem mass spectrometry. The in-depth information obtained from this method including the disaccharide compositions, glycan structures, peptide abundances, and site-specific glycan occupancies provides a detailed profiling of a single spot of tissue which has the potential to be disseminated to biomedical laboratories.
基于质谱的复杂生物样本异质糖蛋白质组研究是一种绘制糖组和蛋白质组结构、功能及动态变化的有力方法。对整个湿组织进行采样通常能提供大量起始材料;然而,在下游处理步骤之前,组织处理存在一定程度的变异性,并且很难从特定区域捕获所有不同的生物分子。本章方案中概述的载玻片上组织消化方法是一种简单且经济高效的方法,可对直径为1毫米或更大的单个组织斑点进行糖蛋白质组的全面绘制。它能在组织载玻片上选择适合10纳升或更大组织体积的目标区域,这相当于将1微升酶溶液滴加到10微米厚组织切片上直径为1毫米的目标区域。对新鲜冷冻或福尔马林固定石蜡包埋组织载玻片表面的生物分子进行连续酶促消化和脱盐,无需任何预先衍生化,就能使用液相色谱 - 串联质谱同时鉴定糖胺聚糖二糖(如透明质酸、硫酸软骨素和硫酸乙酰肝素)、天冬酰胺或N - 连接聚糖以及完整的(糖基化)肽段。通过该方法获得的深入信息,包括二糖组成、聚糖结构、肽丰度和位点特异性聚糖占据情况,可提供单个组织斑点的详细图谱,有可能推广到生物医学实验室。