RT Journal Article
SR Electronic
T1 Structural Basis for the High-Affinity Inhibition of Mammalian Membranous Adenylyl Cyclase by 2',3'-O-(N-Methylanthraniloyl)-Inosine 5'-Triphosphate
JF Molecular Pharmacology
JO Mol Pharmacol
FD American Society for Pharmacology and Experimental Therapeutics
SP mol.111.071894
DO 10.1124/mol.111.071894
A1 Melanie Hubner
A1 Anshuman Dixit
A1 Tung-Chung Mou
A1 Gerald H Lushington
A1 Cibele Pinto
A1 Andreas Gille
A1 Jens Geduhn
A1 Burkhard Konig
A1 Stephen R Sprang
A1 Roland Seifert
YR 2011
UL http://molpharm.aspetjournals.org/content/early/2011/04/15/mol.111.071894.abstract
AB 2',3'-O-(N-Methylanthraniloyl)-inosine 5'-triphosphate (MANT-ITP) is the most potent inhibitor of mammalian membranous adenylyl cyclase (mAC) 5 (AC5, Ki, 1 nM) yet discovered and surpasses the potency of 2',3'-O-(N-methylanthraniloyl)-guanosine 5'-triphosphate (MANT-GTP) 55-fold (Göttle et al., J Pharmacol Exp Ther 329:1156-1165 (2009)). AC5 inhibitors may be valuable drugs for treatment of heart failure. The aim of this study was to elucidate the structural basis for the high-affinity inhibition of mAC by MANT-ITP. MANT-ITP was a considerably more potent inhibitor of the purified catalytic domains VC1 and IIC2 of mAC than MANT-GTP (Ki, 0.7 nM versus 18 nM). Moreover, there was considerably more efficient fluorescence resonance energy transfer between W1020 of IIC2 and the MANT-group of MANT-ITP compared to MANT-GTP, indicating optimal interaction of the MANT-group of MANT-ITP with the hydrophobic pocket. The crystal structure of MANT-ITP in complex with the Gsalpha- and forskolin-activated catalytic domains VC1:IIC2 in comparison to the existing MANT-GTP crystal structure revealed only subtle differences in binding mode. The higher affinity of MANT-ITP to mAC compared to MANT-GTP is probably due to fewer stereochemical constraints upon the nucleotide base in the purine binding pocket, allowing a stronger interaction with the hydrophobic regions of IIC2 domain, as assessed by fluorescence spectroscopy. Stronger interaction is also achieved in the phosphate-binding site. The triphosphate group of MANT-ITP exhibits better metal coordination than the triphosphate group of MANT-GTP, as confirmed by molecular dynamics simulations. Collectively, the subtle differences in ligand structure have profound effects on affinity for mAC.