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3-O-硫酸化硫酸乙酰肝素检测与表征的最新分析进展

Recent analytical advances in the detection and characterization of 3-O-sulfated heparan sulfate.

作者信息

Mernie Elias, Zaia Joseph

机构信息

Department of Biochemistry & Cell Biology, Center for Biomedical Mass Spectrometry, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA, 02118, USA.

出版信息

Anal Bioanal Chem. 2025 May 6. doi: 10.1007/s00216-025-05898-w.

Abstract

Heparan sulfate (HS) is a linear, highly sulfated, and heterogeneous polysaccharide that covalently attaches to core proteins to form heparan sulfate proteoglycans (HSPGs). HSPGs are widely expressed in mammalian cells and are found on the cell surface and within the extracellular matrix (ECM). Structurally, HS consists of repeating disaccharide units composed of hexuronic acid (HexA) (either glucuronic acid (GlcA) or iduronic acid (IdoA)) linked to glucosamine (GlcN) units. The HS chain undergoes extensive post-polymerization modifications, including N-deacetylation of GlcN, C5-epimerization of HexA, and sulfation at various positions like 2-O-sulfation of HexA, as well as 3-O-, 6-O-, and N-sulfation of GlcN. Among these modifications, 3-O-sulfation of HS, produced by HS 3-O-sulfotransferase (HS3OST), is the rarest and most functionally significant. While 3-O-sulfated HS is well known for its anticoagulant properties through the activation of antithrombin, it also plays a critical role in various physiological and pathological processes, including cell differentiation, cancer progression, herpes simplex virus entry, and neuronal development. However, the precise mechanisms underlying these functions and their pathological implications remain inadequately characterized. This knowledge gap is primarily due to the low abundance of 3-O-sulfated HS and the lack of standardized analytical methods for its detection in biological samples. In this review, we summarize recent advancements in analytical techniques for the analysis of 3-O-sulfated HS and highlight potential future directions to improve its characterization and advance our understanding of its biological roles.

摘要

硫酸乙酰肝素(HS)是一种线性、高度硫酸化且不均一的多糖,它共价连接到核心蛋白上形成硫酸乙酰肝素蛋白聚糖(HSPG)。HSPG在哺乳动物细胞中广泛表达,存在于细胞表面和细胞外基质(ECM)中。从结构上看,HS由重复的二糖单元组成,这些二糖单元由己糖醛酸(HexA)(葡萄糖醛酸(GlcA)或艾杜糖醛酸(IdoA))与葡萄糖胺(GlcN)单元相连。HS链经历广泛的聚合后修饰,包括GlcN的N - 去乙酰化、HexA的C5 - 差向异构化以及在不同位置的硫酸化,如HexA的2 - O - 硫酸化,以及GlcN的3 - O - 、6 - O - 和N - 硫酸化。在这些修饰中,由HS 3 - O - 硫酸转移酶(HS3OST)产生的HS的3 - O - 硫酸化是最罕见且功能上最重要的。虽然3 - O - 硫酸化的HS因其通过激活抗凝血酶的抗凝血特性而广为人知,但它在各种生理和病理过程中也起着关键作用,包括细胞分化、癌症进展、单纯疱疹病毒进入和神经元发育。然而,这些功能背后的确切机制及其病理意义仍未得到充分表征。这一知识空白主要是由于3 - O - 硫酸化的HS丰度低以及缺乏用于在生物样品中检测它的标准化分析方法。在本综述中,我们总结了用于分析3 - O - 硫酸化HS的分析技术的最新进展,并强调了潜在的未来方向,以改善其表征并推进我们对其生物学作用的理解。

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