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葡糖醛酸 C5-差向异构酶,一种在硫酸乙酰肝素/肝素生物合成中将葡糖醛酸转化为艾杜糖醛酸的酶。

Glucuronyl C5-epimerase an enzyme converting glucuronic acid to iduronic acid in heparan sulfate/heparin biosynthesis.

机构信息

Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.

出版信息

Prog Mol Biol Transl Sci. 2010;93:59-78. doi: 10.1016/S1877-1173(10)93004-4.

Abstract

The glucuronyl C5 epimerase (HSepi) is one of the modification enzymes involved in biosynthesis of heparan sulfate (HS) and heparin, catalyzing the epimerization of D-glucuronic acid (GlcA) to L-iduronic acid (IdoA) at polymer level. IdoA is critical for HS and heparin to interact with protein ligands, because of its flexible conformation. Although the enzyme recognizes both GlcA and IdoA as substrates catalyzing a reversible reaction of the hexuronic acids in vitro, the reaction appears irreversible in vivo. Targeted interruption of the gene, Glce, in mice resulted in neonatal lethality accompanied with kidney agenesis, premature lung, and skeletal malformations, demonstrating that the single gene coded enzyme is essential for animal development. Elimination of the enzyme resulted in abnormal HS and heparin structure that completely lacks IdoA residues. Loss of 2-O-sulfation due to lacking IdoA in HS chains appears compensated by increased N- and O-sulfation of the glucosamine residues. Recombinant HSepi is used to generate HS/heparin related compounds having potential to be used for therapeutic purposes.

摘要

葡糖醛酸 C5 差向异构酶(HSepi)是参与肝素硫酸(HS)和肝素生物合成的修饰酶之一,在聚合物水平上催化 D-葡萄糖醛酸(GlcA)向 L-艾杜糖醛酸(IdoA)的差向异构化。IdoA 对 HS 和肝素与蛋白配体相互作用至关重要,因为其具有灵活的构象。尽管该酶识别 GlcA 和 IdoA 作为体外催化六糖醛酸可逆反应的底物,但该反应在体内似乎是不可逆的。在小鼠中靶向中断基因 Glce 导致新生鼠死亡,伴有肾发育不全、肺早熟和骨骼畸形,表明该单基因编码的酶对动物发育至关重要。该酶的缺失导致 HS 和肝素结构异常,完全缺乏 IdoA 残基。由于 HS 链中缺乏 IdoA,2-O-磺酸化的缺失似乎通过增加葡萄糖胺残基的 N-和 O-磺酸化得到补偿。重组 HSepi 用于生成具有治疗用途潜力的 HS/肝素相关化合物。

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