Home LiteratureArticle Details
PMID: 2162349 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Probing the cyclic nucleotide binding sites of cAMP-dependent protein kinases I and II with analogs of adenosine 3',5'-cyclic phosphorothioates.

The Journal of biological chemistry ·Vol. 265 ·No. 18 ·1990-06-25 ·Pages 10484-91

Dostmann WR, Taylor SS, Genieser HG, Jastorff B, Døskeland SO, Ogreid D

Abstract

A set of cAMP analogs were synthesized that combined exocyclic sulfur substitutions in the equatorial (Rp) or the axial (Sp) position of the cyclophosphate ring with modifications in the adenine base of cAMP. The potency of these compounds to inhibit the binding of [3H]cAMP to sites A and B from type I (rabbit skeletal muscle) and type II (bovine myocardium) cAMP-dependent protein kinase was determined quantitatively. On the average, the Sp isomers had a 5-fold lower affinity for site A and a 30-fold lower affinity for site B of isozyme I than their cyclophosphate homolog. The mean reduction in affinities for the equivalent sites of isozyme II were 20- and 4-fold, respectively. The Rp isomers showed a decrease in affinity of approximately 400-fold and 200-fold for site A and B, respectively, of isozyme I, against 200-fold and 45-fold for site A and B of isozyme II. The Sp substitutions therefore increased the relative preference for site A of isozyme I and site B of isozyme II. The Rp substitution, on the other hand, increased the relative preference for site B of both isozymes. These data show that the Rp and Sp substitutions are tolerated differently by the two intrachain sites of isozymes I and II. They also support the hypothesis that it is the axial, and not the previously proposed equatorial oxygen that contributes the negative charge for the ionic interaction with an invariant arginine in all four binding sites. In addition, they demonstrate that combined modifications in the adenine ring and the cyclic phosphate ring of cAMP can enhance the ability to discriminate between site A and B of one isozyme as well as to discriminate between isozyme I and II. Since Rp analogs of cAMP are known to inhibit activation of cAMP-dependent protein kinases, the findings of the present study have implications for the synthesis of analogs having a very high selectivity for isozyme I or II.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Binding, Competitive Cattle Cyclic AMP/analogs & derivatives,chemical synthesis,metabolism Isoenzymes/metabolism Macromolecular Substances Models, Molecular Molecular Conformation Molecular Sequence Data Muscles/enzymology Myocardium/enzymology Protein Conformation Protein Kinases/metabolism Rabbits Structure-Activity Relationship Thionucleotides/chemical synthesis,metabolism
Chemicals
Isoenzymes Macromolecular Substances Thionucleotides adenosine-3',5'-cyclic phosphorothioate Cyclic AMP Protein Kinases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dostmann W R
Department of Chemistry, University of California, San Diego, La Jolla 92093.
Taylor S S
Genieser H G
Jastorff B
Døskeland S O
Ogreid D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1990-06-25
Pages
10484-91
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM-34921 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com