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3-酮脂酰辅酶A硫解酶在体外向大鼠肝脏过氧化物酶体的翻译后导入

Post-translational import of 3-ketoacyl-CoA thiolase into rat liver peroxisomes in vitro.

作者信息

Miura S, Miyazawa S, Osumi T, Hashimoto T, Fujiki Y

机构信息

Meiji Institute of Health Science, Kanagawa.

出版信息

J Biochem. 1994 Jun;115(6):1064-8. doi: 10.1093/oxfordjournals.jbchem.a124458.

Abstract

Cell-free translation products of hepatic free polysomal RNA from a clofibrate-treated rat were incubated at 26 degrees C for 0-60 min with a post-heavy mitochondrial supernatant fraction from normal rat liver. Exogenously added proteinase K-resistant precursor and mature forms of peroxisomal 3-ketoacyl-CoA thiolase were recovered in a particulate fraction and increased with time. Both forms of thiolase cosedimented with peroxisomes, when the proteinase K-treated import reaction mixture was centrifuged in a sucrose density gradient. The in vitro import and processing of thiolase precursors, types A and B, was likewise reproduced with highly purified peroxisomes. These results strongly suggest that the precursor form of 3-ketoacyl-CoA thiolase is translocated into peroxisomes, apparently without tight coupling with proteolytic processing to the mature protein.

摘要

将氯贝丁酯处理的大鼠肝脏游离多聚核糖体RNA的无细胞翻译产物,与正常大鼠肝脏的重线粒体后上清液组分在26℃孵育0 - 60分钟。外源添加的蛋白酶K抗性过氧化物酶体3-酮酰基辅酶A硫解酶前体和成熟形式在颗粒组分中回收,且随时间增加。当蛋白酶K处理的导入反应混合物在蔗糖密度梯度中离心时,两种形式的硫解酶都与过氧化物酶体共沉降。硫解酶A和B前体的体外导入和加工,同样可以用高度纯化的过氧化物酶体重现。这些结果有力地表明,3-酮酰基辅酶A硫解酶的前体形式被转运到过氧化物酶体中,显然与成熟蛋白的蛋白水解加工没有紧密偶联。

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