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过氧化物酶体膜多肽的体外合成。

In vitro synthesis of peroxisomal membrane polypeptides.

作者信息

Köster A, Heisig M, Heinrich P C, Just W W

出版信息

Biochem Biophys Res Commun. 1986 Jun 13;137(2):626-32. doi: 10.1016/0006-291x(86)91124-1.

Abstract

Peroxisomal membranes containing predominantly integral peroxisome membrane polypeptides were obtained from a highly purified peroxisomal fraction. Following sodium dodecylsulfate polyacrylamide gel electrophoresis three polypeptides with apparent molecular weights of 69, 36, and 22 kDa were isolated and used to raise antibodies in rabbits. Cell-free synthesis of these polypeptides was carried out in an in vitro translational system derived from rabbit reticulocytes. By subjecting peroxisomal membranes to reductive methylation [14C]-radiolabeled mature membrane polypeptides were obtained. The comparison of the three mature integral peroxisome membrane polypeptides with their corresponding in vitro synthesis products revealed no size differences indicating the lack of recognizable presequences for these peroxisomal membrane polypeptides.

摘要

含有主要为整合型过氧化物酶体膜多肽的过氧化物酶体膜是从高度纯化的过氧化物酶体组分中获得的。经过十二烷基硫酸钠聚丙烯酰胺凝胶电泳后,分离出了表观分子量分别为69、36和22 kDa的三种多肽,并用于在兔体内产生抗体。这些多肽的无细胞合成是在源自兔网织红细胞的体外翻译系统中进行的。通过对过氧化物酶体膜进行还原甲基化,获得了[14C]放射性标记的成熟膜多肽。将三种成熟的整合型过氧化物酶体膜多肽与其相应的体外合成产物进行比较,未发现大小差异,表明这些过氧化物酶体膜多肽缺乏可识别的前导序列。

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