SPLEEN PROTEIN TYROSINE KINASES TPK-IIB AND CSK DISPLAY DIFFERENT IMMUNOREACTIVITY AND OPPOSITE SPECIFICITES TOWARD C-SRC-DERIVED PEPTIDES

被引:33
作者
BRUNATI, AM
ALLEE, G
MARIN, O
DONELLADEANA, A
CESARO, L
BOUGERET, C
FAGARD, R
BENAROUS, R
FISCHER, S
PINNA, LA
机构
[1] UNIV PADUA,CNR,DIPARTIMENTO CHIM BIOL,VIA TRIESTE 75,I-35121 PADUA,ITALY
[2] UNIV PADUA,CNR,CTR FISIOL MITOCONDRIALE,I-35121 PADUA,ITALY
[3] INSERM,U332,F-75005 PARIS,FRANCE
关键词
PROTEIN TYROSINE KINASE; PP60(C-SRC) REGULATION; PHOSPHOTYROSINE; PEPTIDE; SPLEEN;
D O I
10.1016/0014-5793(92)81212-5
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
Polyclonal antibodies have been raised against two synthetic peptides reproducing the 48-64 and 353-369 sequences of CSK, a protein tyrosine kinase implicated in the down-regulation of src-related protein kinases. Both antibodies specifically recognize recombinant CSK and a CSK-related 49 kDa protein tyrosine kinase present in spleen but they do not cross-react with purified TPK-IIB, a spleen protein tyrosine kinase sharing with CSK catalytic activity toward src kinases and incapability to autophosphorylate. CSK and TPK-IIB once resolved from each other by heparin-Sepharose affinity chromatography, display opposite specificities toward synthetic peptides reproducing the sequences around the main phosphoacceptor ceptor residues of pp60c-src, namely Tyr-416 and Tyr-527. These data support the view that TPK-IIB and CSK may exert opposite effects on the activity of src-related protein tyrosine kinases.
引用
收藏
页码:291 / 294
页数:4
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