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从无序到有序:硫酸乙酰肝素中配体结合位点的组装

Order out of chaos: assembly of ligand binding sites in heparan sulfate.

作者信息

Esko Jeffrey D, Selleck Scott B

机构信息

Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California at San Diego, La Jolla, California, 92093-0687, USA.

出版信息

Annu Rev Biochem. 2002;71:435-71. doi: 10.1146/annurev.biochem.71.110601.135458. Epub 2001 Nov 9.

Abstract

Virtually every cell type in metazoan organisms produces heparan sulfate. These complex polysaccharides provide docking sites for numerous protein ligands and receptors involved in diverse biological processes, including growth control, signal transduction, cell adhesion, hemostasis, and lipid metabolism. The binding sites consist of relatively small tracts of variably sulfated glucosamine and uronic acid residues in specific arrangements. Their formation occurs in a tissue-specific fashion, generated by the action of a large family of enzymes involved in nucleotide sugar metabolism, polymer formation (glycosyltransferases), and chain processing (sulfotransferases and an epimerase). New insights into the specificity and organization of the biosynthetic apparatus have emerged from genetic studies of cultured cells, nematodes, fruit flies, zebrafish, rodents, and humans. This review covers recent developments in the field and provides a resource for investigators interested in the incredible diversity and specificity of this process.

摘要

后生动物体内几乎每种细胞类型都会产生硫酸乙酰肝素。这些复杂的多糖为众多参与多种生物过程的蛋白质配体和受体提供了停靠位点,这些生物过程包括生长控制、信号转导、细胞黏附、止血和脂质代谢。结合位点由特定排列的相对较小的可变硫酸化葡糖胺和糖醛酸残基片段组成。它们以组织特异性的方式形成,由参与核苷酸糖代谢、聚合物形成(糖基转移酶)和链加工(磺基转移酶和差向异构酶)的一大类酶的作用产生。对培养细胞、线虫、果蝇、斑马鱼、啮齿动物和人类的遗传学研究,为生物合成装置的特异性和组织方式带来了新的见解。本综述涵盖了该领域的最新进展,并为对这一过程令人难以置信的多样性和特异性感兴趣的研究人员提供了参考资源。

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