Adenine Nucleoside 3′-Tetraphosphates Are Novel and Potent Inhibitors of Adenylyl Cyclases
Copyright policy )Adenine Nucleoside 3′-Tetraphosphates Are Novel and Potent Inhibitors of Adenylyl Cyclases
2'-Deoxyadenosine 3'-tetraphosphate (2'-deoxy-3'-A4P) and 2', 5'-dideoxyadenosine 3'-tetraphosphate (2',5'-dideoxy-3'-A4P) were synthesized, and their effects were tested on crude and purified forms of native adenylyl cyclases isolated from brain. Syntheses combined the method of alkoxide activation with the use of tribromoethyl phosphoromorpholino-chloridate as an initial phosphorylating agent. Inhibition of adenylyl cyclase was rapid in onset. With 2'-d-3'-A4P or 2',5'-dd-3'-A4P inhibition of a purified native enzyme conformed to a linear noncompetitive behavior with respect to substrate, metal-5'ATP. Order of potency was 2', 5'-dideoxy- > 2'-deoxyadenosine and 3'-tetraphosphate > 3'-triphosphate. Both mechanism of inhibition and rank order of potency were consistent with inhibition via the 3'-nucleotide-(P)-site on adenylyl cyclase. Neither 2',5'-dd-3'-ATP nor 2',5'-dd-3'-A4P had any effect on the activities of other adenosine nucleotide binding proteins such as Ca2+/calmodulin-sensitive cyclic nucleotide phosphodiesterase, Na+/K+-ATPase, or cAMP-dependent protein kinase. With purified adenylyl cyclase from bovine brain 2',5'-dd-3'-A4P and 2'-d-3'-A4P gave, respectively, IC50 values of 9.3 and 15 nM and Ki values of 23 and 53 nM. These 3'-nucleotides are the most potent regulators described for adenylyl cyclases.
- State University of New York at Potsdam United States
- State University of New York United States
Binding Sites, Phosphoric Diester Hydrolases, Brain, Cyclic Nucleotide Phosphodiesterases, Type 1, Cyclic AMP-Dependent Protein Kinases, Rats, Kinetics, Structure-Activity Relationship, Deoxyadenine Nucleotides, 3',5'-Cyclic-AMP Phosphodiesterases, 3',5'-Cyclic-GMP Phosphodiesterases, Adenylyl Cyclase Inhibitors, Animals, Cattle, Indicators and Reagents, Sodium-Potassium-Exchanging ATPase, Adenylyl Cyclases, Dideoxynucleotides
Binding Sites, Phosphoric Diester Hydrolases, Brain, Cyclic Nucleotide Phosphodiesterases, Type 1, Cyclic AMP-Dependent Protein Kinases, Rats, Kinetics, Structure-Activity Relationship, Deoxyadenine Nucleotides, 3',5'-Cyclic-AMP Phosphodiesterases, 3',5'-Cyclic-GMP Phosphodiesterases, Adenylyl Cyclase Inhibitors, Animals, Cattle, Indicators and Reagents, Sodium-Potassium-Exchanging ATPase, Adenylyl Cyclases, Dideoxynucleotides
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