EXPRESSION AND CHARACTERIZATION OF PROTEIN-KINASE C-DELTA
被引:103
|
作者:
OLIVIER, AR
论文数: 0引用数: 0
h-index: 0
机构:
IMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,44 LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLANDIMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,44 LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLAND
OLIVIER, AR
[1
]
PARKER, PJ
论文数: 0引用数: 0
h-index: 0
机构:
IMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,44 LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLANDIMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,44 LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLAND
PARKER, PJ
[1
]
机构:
[1] IMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,44 LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLAND
来源:
EUROPEAN JOURNAL OF BIOCHEMISTRY
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1991年
/
200卷
/
03期
关键词:
D O I:
10.1111/j.1432-1033.1991.tb16248.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 M(r) of PKC-delta as determined by SDS/PAGE and immunoblot analysis using anti-(PKC-delta C-terminal) antibodies was 77000. 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.