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小鼠β2-糖蛋白I(载脂蛋白H)的表征、表达及进化

Characterization, expression and evolution of mouse beta 2-glycoprotein I (apolipoprotein H).

作者信息

Sellar G C, Steel D M, Zafiropoulos A, Seery L T, Whitehead A S

机构信息

Department of Genetics, Trinity College, Dublin, Ireland.

出版信息

Biochem Biophys Res Commun. 1994 May 16;200(3):1521-8. doi: 10.1006/bbrc.1994.1623.

Abstract

beta 2-glycoprotein I (beta 2I) is a 50kDa serum glycoprotein of ill defined function. Based upon its capacity to bind negatively charged phospholipids a number of possible inhibitory roles for beta 2I have been proposed. We have cloned and sequenced a full length mouse beta 2I cDNA clone and demonstrated that mouse beta 2I does not behave as an acute phase reactant following an experimentally induced inflammation. Phylogenetic analysis of the known mammalian beta 2I homologues has provided evidence that mouse beta 2I is the most divergent and is evolving at a faster rate than beta 2I in other species.

摘要

β2-糖蛋白I(β2I)是一种功能不明的50kDa血清糖蛋白。基于其结合带负电荷磷脂的能力,已提出β2I的一些可能的抑制作用。我们克隆并测序了一个全长小鼠β2I cDNA克隆,并证明在实验诱导的炎症后,小鼠β2I不作为急性期反应物。对已知哺乳动物β2I同源物的系统发育分析提供了证据,表明小鼠β2I是最具差异的,并且其进化速度比其他物种的β2I更快。

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