Suppr超能文献

蛋白激酶C-δ的表达与特性分析

Expression and characterization of protein kinase C-delta.

作者信息

Olivier A R, Parker P J

机构信息

Protein Phosphorylation Laboratory, Imperial Cancer Research Fund, London, England.

出版信息

Eur J Biochem. 1991 Sep 15;200(3):805-10. doi: 10.1111/j.1432-1033.1991.tb16248.x.

Abstract

A cDNA encoding protein kinase C-delta (PKC-delta) was isolated from a rat brain library. The coding region was subcloned into the expression vector pmt2 and transfected into COS-1 cells. Expression of the protein led to an 11-fold increase in activity as determined with a synthetic peptide based on the PKC-delta pseudosubstrate site. The Mr of PKC-delta as determined by SDS/PAGE and immunoblot analysis using anti-(PKC-delta C-terminal) antibodies was 77,000. The enzyme was purified to near homogeneity and showed total dependency on phospholipid and diacylglycerol (or phorbol esters) for activity. Like PKC-epsilon, PKC-delta displays no Ca2+ dependence for activation. The substrate specificity of PCK-delta is similar to that of PKC-epsilon but quite different from other PKCs.

摘要

从大鼠脑文库中分离出一种编码蛋白激酶C-δ(PKC-δ)的cDNA。将编码区亚克隆到表达载体pmt2中,并转染到COS-1细胞中。用基于PKC-δ假底物位点的合成肽测定,该蛋白的表达导致活性增加了11倍。通过SDS/PAGE和使用抗(PKC-δ C末端)抗体的免疫印迹分析确定,PKC-δ的Mr为77,000。该酶被纯化至接近均一,并且其活性完全依赖于磷脂和二酰基甘油(或佛波酯)。与PKC-ε一样,PKC-δ的激活不依赖Ca2+。PKC-δ的底物特异性与PKC-ε相似,但与其他蛋白激酶C有很大不同。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验