Crystal structure of human phosphodiesterase 3B: atomic basis for substrate and inhibitor specificity.

Abstract

Phosphodiesterases (PDEs) are enzymes that modulate cyclic nucleotide signaling and as such are clinical targets for a range of disorders including congestive heart failure, erectile dysfunction, and inflammation. The PDE3 family comprises two highly homologous subtypes expressed in different tissues, and inhibitors of this family have been shown to increase lipolysis in adipocytes. A specific PDE3B (the lipocyte-localized subtype) inhibitor would be a very useful tool to evaluate the effects of PDE3 inhibition on lipolysis and metabolic rate and might become a novel tool for treatment of obesity. We report here the three-dimensional structures of the catalytic domain of human PDE3B in complex with a generic PDE inhibitor and a novel PDE3 selective inhibitor. These structures explain the dual cAMP/cGMP binding capabilities of PDE3, provide the molecular basis for inhibitor specificity, and can supply a valid platform for the design of improved compounds.

• Authors: Giovanna Scapin, Sangita B Patel, Christine Chung, Jeffrey P Varnerin, Scott D Edmondson, Anthony Mastracchio, Emma R Parmee, Suresh B Singh, Joseph W Becker, Lex H T Van der Ploeg, Michael R Tota
• Journal: Biochemistry (Biochemistry) Vol. 43 Issue 20 Pg. 6091-100 (May 25 2004) ISSN: 0006-2960 [Print] United States
• PMID: 15147193 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Isoenzymes
• Phosphodiesterase Inhibitors
• 3',5'-Cyclic-AMP Phosphodiesterases
• Cyclic Nucleotide Phosphodiesterases, Type 3
• PDE3B protein, human
• Cyclic GMP
• 1-Methyl-3-isobutylxanthine

Topics

• 1-Methyl-3-isobutylxanthine (chemistry, metabolism)
• 3',5'-Cyclic-AMP Phosphodiesterases (chemistry, genetics, metabolism)
• Catalytic Domain
• Crystallography, X-Ray
• Cyclic GMP (chemistry)
• Cyclic Nucleotide Phosphodiesterases, Type 3
• Dimerization
• Humans
• Isoenzymes (chemistry, genetics, metabolism)
• Models, Molecular
• Molecular Structure
• Mutagenesis, Site-Directed
• Phosphodiesterase Inhibitors (chemistry, metabolism)
• Protein Structure, Tertiary
• Substrate Specificity