Isozyme-specific inhibition of protein kinase C by RNA aptamers

In vitro selection technology has been used to purify RNA aptamers from a random sequence pool that can bind to, and specifically inhibit, protein kinase C beta II. Two of the selected RNA aptamers bind to this isozyme of protein kinase C with nanomolar affinities and inhibit activation with unprece...

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Veröffentlicht in:The Journal of biological chemistry 1994-12, Vol.269 (51), p.32051-32054
Hauptverfasser: Conrad, R, Keranen, L M, Ellington, A D, Newton, A C
Format: Artikel
Sprache:eng
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Zusammenfassung:In vitro selection technology has been used to purify RNA aptamers from a random sequence pool that can bind to, and specifically inhibit, protein kinase C beta II. Two of the selected RNA aptamers bind to this isozyme of protein kinase C with nanomolar affinities and inhibit activation with unprecedented selectivity; the highly related, alternatively spliced beta I isozyme, which differs by 23 residues, is inhibited with 1 order of magnitude lower potency; the next most similar isozyme, alpha, shows no detectable inhibition. The production of isozyme-specific inhibitors of protein kinase C opens the possibilities for dissecting the roles of specific protein kinase Cs in the myriad of intracellular signalling pathways.
ISSN:0021-9258
1083-351X
DOI:10.1016/S0021-9258(18)31598-9