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硫酸乙酰肝素和肝素的酶促合成。

Enzymatic synthesis of heparan sulfate and heparin.

作者信息

Joice April, Raman Karthik, Mencio Caitlin, Quintero Maritza V, Brown Spencer, Nguyen Thao Kim Nu, Kuberan Balagurunathan

机构信息

Department of Medicinal Chemistry, University of Utah, 30 South 2000 East, Skaggs #307, Salt Lake City, UT, 84112, USA.

出版信息

Methods Mol Biol. 2015;1229:11-9. doi: 10.1007/978-1-4939-1714-3_2.

Abstract

Heparan sulfate (HS) polysaccharide chains have been shown to orchestrate distinct biological functions in several systems. Study of HS structure-function relations is, however, hampered due to the lack of availability of HS in sufficient quantities as well as the molecular heterogeneity of naturally occurring HS. Enzymatic synthesis of HS is an attractive alternative to the use of naturally occurring HS, as it reduces molecular heterogeneity, or a long and daunting chemical synthesis of HS. Heparosan, produced by E. coli K5 bacteria, has a structure similar to the unmodified HS backbone structure and can be used as a precursor in the enzymatic synthesis of HS-like polysaccharides. Here, we describe an enzymatic approach to synthesize several specifically sulfated HS polysaccharides for biological studies using the heparosan backbone and a combination of recombinant biosynthetic enzymes such as C5-epimerase and sulfotransferases.

摘要

硫酸乙酰肝素(HS)多糖链已被证明在多个系统中协调不同的生物学功能。然而,由于缺乏足够数量的HS以及天然存在的HS的分子异质性,HS结构-功能关系的研究受到了阻碍。HS的酶促合成是使用天然存在的HS的一种有吸引力的替代方法,因为它减少了分子异质性,或者避免了HS漫长而艰巨的化学合成。大肠杆菌K5细菌产生的类肝素具有与未修饰的HS主链结构相似的结构,可作为酶促合成类HS多糖的前体。在这里,我们描述了一种酶促方法,使用类肝素主链和重组生物合成酶(如C5-表异构酶和磺基转移酶)的组合来合成几种用于生物学研究的特定硫酸化HS多糖。

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