Alotaibi Faizah S, Alsadun Marim M R, Alsaiari Sarah A, Ramakrishnan Krithika, Yates Edwin A, Fernig David G
Department of Biochemistry, Systems and Cell Biology, Institute of Molecular, Integrative and Systems Biology, University of Liverpool, Liverpool L69 7ZB, U.K.
Department of Biology, University of Tabuk, Tabuk 71491, Saudi Arabia.
Essays Biochem. 2024 Dec 4;68(4):479-489. doi: 10.1042/EBC20230093.
Heparan sulfate (HS) is a glycosaminoglycan, polysaccharides that are considered to have arisen in the last common unicellular ancestor of multicellular animals. In this light, the large interactome of HS and its myriad functions in relation to the regulation of cell communication are not surprising. The binding of proteins to HS determines their localisation and diffusion, essential for embryonic development and homeostasis. Following the biosynthesis of the initial heparosan polymer, the subsequent modifications comprise an established canonical pathway and a minor pathway. The more frequent former starts with N-deacetylation and N-sulfation of GlcNAc residues, the latter with C-5 epimerisation of a GlcA residue adjacent to a GlcNAc. The binding of proteins to HS is driven by ionic interactions. The multivalent effect arising from the many individual ionic bonds between a single protein and a polysaccharide chain results in a far stronger interaction than would be expected from an ion-exchange process. In many instances, upon binding, both parties undergo substantial conformational change, the resulting hydrogen and van der Waal bonds contributing significant free energy to the binding reaction. Nevertheless, ionic bonds dominate the protein-polysaccharide interaction kinetically. Together with the multivalent effect, this provides an explanation for the observed trapping of HS-binding proteins in extracellular matrix. Importantly, individual ionic bonds have been observed to be dynamic; breaking and reforming, while the protein remains bound to the polysaccharide. These considerations lead to a model for 1D diffusion of proteins in extracellular matrix on HS, involving mechanisms such as sliding, chain switching and rolling.
硫酸乙酰肝素(HS)是一种糖胺聚糖,这类多糖被认为出现在多细胞动物的最后一个共同单细胞祖先中。鉴于此,HS庞大的相互作用组及其在细胞通讯调节方面的众多功能就不足为奇了。蛋白质与HS的结合决定了它们的定位和扩散,这对胚胎发育和体内平衡至关重要。在最初的乙酰肝素聚合物生物合成之后,随后的修饰包括一条既定的经典途径和一条次要途径。更常见的前者始于GlcNAc残基的N-脱乙酰化和N-硫酸化,后者始于与GlcNAc相邻的GlcA残基的C-5差向异构化。蛋白质与HS的结合是由离子相互作用驱动的。单个蛋白质与多糖链之间许多单个离子键产生的多价效应导致的相互作用比离子交换过程预期的要强得多。在许多情况下,结合时双方都会发生显著的构象变化,由此产生的氢键和范德华键为结合反应贡献了大量自由能。然而,离子键在动力学上主导着蛋白质-多糖相互作用。与多价效应一起,这为观察到的HS结合蛋白被困在细胞外基质中提供了解释。重要的是,已观察到单个离子键是动态的;在蛋白质仍与多糖结合时会断裂和重新形成。这些考虑因素导致了一个蛋白质在细胞外基质中HS上进行一维扩散的模型,涉及滑动、链切换和滚动等机制。