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载脂蛋白A在脂蛋白A组装中的结构要求。

Structural requirements of apo-a for the lipoprotein-a assembly.

作者信息

Frank S, Durovic S, Kostner G M

机构信息

Institute of Medical Biochemistry, University of Graz, Austria.

出版信息

Biochem J. 1994 Nov 15;304 ( Pt 1)(Pt 1):27-30. doi: 10.1042/bj3040027.

Abstract

Lipoprotein-a [Lp(a)], one of the most atherogenic lipoproteins, is composed of a low-density lipoprotein (LDL) core in addition to an apo-a of variable size which is linked to apoB by a disulphide bridge. Lp(a) synthesized in vitro by incubation of recombinant apo-a (r-apo-a) with LDL is physico-chemically indistinguishable from native Lp(a). The synthesis of Lp(a) in vitro proceeds in two steps. In the first step, one of the unique kringle-IVs (K-IVs) in apo-a binds to a Lys residue of apoB; in the second step, Cys-4057 of K-IV type-9 (T-9) forms a disulphide bridge with Cys-3734 of LDL. Here we have produced r-apo-a with different combinations of unique K-IVs and shown that K-IV T-6 is required for the first step of Lp(a) assembly. For the second step not only is K-IV T-9 essential, but also the distance between T-6 and T-9 requires a length of two K-IVs. These findings give additional insight into the mode of Lp(a) assembly and are of relevance in the search for apo-a mutants influencing Lp(a) levels and for the development of Lp(a)-lowering medications.

摘要

脂蛋白-a [Lp(a)] 是最具致动脉粥样硬化性的脂蛋白之一,除了一个大小可变的载脂蛋白-a(apo-a)外,还由一个低密度脂蛋白(LDL)核心组成,该载脂蛋白-a通过二硫键与载脂蛋白B(apoB)相连。通过将重组载脂蛋白-a(r-apo-a)与LDL一起孵育在体外合成的Lp(a)在物理化学性质上与天然Lp(a)无法区分。Lp(a)的体外合成分两步进行。第一步,apo-a中独特的kringle-IV(K-IV)之一与apoB的一个赖氨酸残基结合;第二步,K-IV 9型(T-9)的半胱氨酸-4057与LDL的半胱氨酸-3734形成二硫键。在这里,我们制备了具有不同独特K-IV组合的r-apo-a,并表明K-IV T-6是Lp(a)组装第一步所必需的。对于第二步,不仅K-IV T-9是必不可少的,而且T-6和T-9之间的距离需要两个K-IV的长度。这些发现为Lp(a)的组装模式提供了更多见解,并且在寻找影响Lp(a)水平的apo-a突变体以及开发降低Lp(a)的药物方面具有相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e0f/1137446/83a45e5abb0e/biochemj00075-0037-a.jpg

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