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使用结构定义的寡糖来理解蛋白质和肝素硫酸之间的相互作用。

Using structurally defined oligosaccharides to understand the interactions between proteins and heparan sulfate.

机构信息

Department of Oral Biology, School of Dental Medicine, University at Buffalo, SUNY, Buffalo, NY 14214, USA.

Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Curr Opin Struct Biol. 2018 Jun;50:155-161. doi: 10.1016/j.sbi.2018.04.003. Epub 2018 Apr 21.


DOI:10.1016/j.sbi.2018.04.003
PMID:29684759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6078804/
Abstract

Heparan sulfate (HS) is widely present on the animal cell surface and in the extracellular matrix. HS achieves its biological functions by interacting with proteins to change proteins' conformation, oligomerization state and cellular location. The challenging question to study HS is how to dissect the relationship between the structures of HS and the biological activities. In the past several years, crucial techniques have been developed to overcome this challenge. A novel chemoenzymatic method to synthesize structurally defined HS oligosaccharides has offered a key access to this class of sulfated carbohydrate molecules. Recent rapid progress of HS microarray technology allows screening of the interaction of a target protein with a large number of HS oligosaccharides. The improved availability of HS oligosaccharides and HS microarray analysis will undoubtedly accelerate the investigation of the contribution of the specific sulfated carbohydrate structures of HS in a wide range of biological contexts.

摘要

硫酸乙酰肝素(HS)广泛存在于动物细胞表面和细胞外基质中。HS 通过与蛋白质相互作用来改变蛋白质的构象、寡聚状态和细胞位置,从而发挥其生物学功能。研究 HS 的一个具有挑战性的问题是如何剖析 HS 的结构与生物学活性之间的关系。在过去的几年中,已经开发出了一些关键技术来克服这一挑战。一种新的化学酶法合成具有结构定义的 HS 寡糖的方法为这类硫酸化碳水化合物分子提供了关键途径。HS 微阵列技术的快速发展使得可以筛选目标蛋白与大量 HS 寡糖的相互作用。HS 寡糖可用性的提高和 HS 微阵列分析无疑将加速研究 HS 特定硫酸化碳水化合物结构在广泛的生物学背景下的贡献。

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本文引用的文献

[1]
Chemoenzymatic synthesis of heparan sulfate and heparin oligosaccharides and NMR analysis: paving the way to a diverse library for glycobiologists.

Chem Sci. 2017-12-1

[2]
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Curr Opin Chem Biol. 2017-10

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Synthetic oligosaccharides can replace animal-sourced low-molecular weight heparins.

Sci Transl Med. 2017-9-6

[4]
Heparan Sulfate Microarray Reveals That Heparan Sulfate-Protein Binding Exhibits Different Ligand Requirements.

J Am Chem Soc. 2017-7-7

[5]
Synthesis of 3-O-Sulfated Oligosaccharides to Understand the Relationship between Structures and Functions of Heparan Sulfate.

J Am Chem Soc. 2017-4-12

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Label-Free Discovery Array Platform for the Characterization of Glycan Binding Proteins and Glycoproteins.

Anal Chem. 2017-3-30

[7]
Construction and characterisation of a heparan sulphate heptasaccharide microarray.

Chem Commun (Camb). 2017-1-31

[8]
Glycosaminoglycanomics: where we are.

Glycoconj J. 2017-6

[9]
Gas-Phase Analysis of the Complex of Fibroblast GrowthFactor 1 with Heparan Sulfate: A Traveling Wave Ion Mobility Spectrometry (TWIMS) and Molecular Modeling Study.

J Am Soc Mass Spectrom. 2016-9-23

[10]
Biological function of unique sulfated glycosaminoglycans in primitive chordates.

Glycoconj J. 2017-6

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