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从大鼠肝脏高尔基体和血浆脂蛋白中分离出的载脂蛋白A-I同工型。

Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma.

作者信息

Tarugi P, Ghisellini M, Pecorari M, Brugni N, Calandra S

出版信息

Atherosclerosis. 1985 Aug;56(2):189-98. doi: 10.1016/0021-9150(85)90018-8.

Abstract

We compared apo A-I isolated from the lipoproteins of the Golgi apparatus of rat liver with apo A-I found in plasma lipoproteins. Golgi apo A-I consists of 3 main isoforms with a molecular weight of approximately 28000 and isoelectric points (pI) of 5.97, 5.88 and 5.76, respectively. Plasma apo A-I consists of 4 major and 3 minor isoforms with a molecular weight of 27000. The pI of the major isoforms (numbered 4-7) is 5.88, 5.80, 5.70 and 5.60, respectively. In order to investigate which of the plasma isoforms derived directly from Golgi apo A-I, [35S]methionine was injected into the portal vein and Golgi and plasma apo A-I were isolated shortly thereafter. While all Golgi isoforms were labelled only 3 isoforms of plasma apo A-I (namely isoforms 5, 6 and 7) were found to be labelled. The major plasma isoform (isoform 4 which accounts for more than 60% of apo A-I mass of plasma HDL) was found to be unlabelled. However, when 35S plasma lipoproteins newly secreted by the liver were incubated in vitro in the presence of heparinized plasma, labelled isoform 4 appeared suggesting that heparinized plasma contained some factor capable of converting isoforms 5-7 into isoform 4. This plasma factor appears to be a protease as the in vitro formation of isoform 4 is prevented by protease inhibitors.

摘要

我们将从大鼠肝脏高尔基体脂蛋白中分离出的载脂蛋白A-I与血浆脂蛋白中的载脂蛋白A-I进行了比较。高尔基体载脂蛋白A-I由3种主要的同工型组成,分子量约为28000,等电点(pI)分别为5.97、5.88和5.76。血浆载脂蛋白A-I由4种主要同工型和3种次要同工型组成,分子量为27000。主要同工型(编号为4 - 7)的pI分别为5.88、5.80、5.70和5.60。为了研究哪种血浆同工型直接来源于高尔基体载脂蛋白A-I,将[35S]甲硫氨酸注入门静脉,随后不久分离高尔基体和血浆载脂蛋白A-I。虽然所有高尔基体同工型都被标记,但发现只有血浆载脂蛋白A-I的3种同工型(即同工型5、6和7)被标记。发现主要的血浆同工型(同工型4,占血浆高密度脂蛋白载脂蛋白A-I质量的60%以上)未被标记。然而,当肝脏新分泌的35S血浆脂蛋白在肝素化血浆存在下进行体外孵育时,出现了标记的同工型4,这表明肝素化血浆中含有某种能够将同工型5 - 7转化为同工型4的因子。这种血浆因子似乎是一种蛋白酶,因为蛋白酶抑制剂可阻止体外同工型4的形成。

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