Identification of an oligodeoxynucleotide sequence motif that specifically inhibits phosphorylation by protein tyrosine kinases

被引:10
作者
Krieg, AM
Matson, S
Cheng, KR
Fisher, E
Koretzky, GA
Koland, JG
机构
[1] VET AFFAIRS MED CTR,IOWA CITY,IA 52246
[2] UNIV IOWA,COLL MED,DEPT PHARMACOL,IOWA CITY,IA 52242
[3] AMGEN BOULDER INC,BOULDER,CO 80301
[4] UNIV IOWA,COLL MED,DEPT PHYSIOL,IOWA CITY,IA 52242
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 1997年 / 7卷 / 02期
关键词
D O I
10.1089/oli.1.1997.7.115
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
Protein tyrosine kinases (PTKs) have central roles in cellular signal transduction. We have identified a sequence motif (CGT[C]GA) in phosphorothioate-modified oligodeoxynucleotides (ODNs) that specifically inhibits the enzymatic activity of recombinant or immunoprecipitated PTK in vitro. Hexamer ODNs containing this motif block both substrate and autophosphorylation of at least four different PTKs but have no apparent effect on the enzymatic activity of a serine/threonine protein kinase. These data suggest possible new applications for ODNs and have implications for the design and interpretation of experiments using antisense or tripler ODNs.
引用
收藏
页码:115 / 123
页数:9
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