Olivier A R, Parker P J
Protein Phosphorylation Laboratory, Imperial Cancer Research Fund, London, England.
Eur J Biochem. 1991 Sep 15;200(3):805-10. doi: 10.1111/j.1432-1033.1991.tb16248.x.
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.
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。