Engineering of A3 adenosine and P2Y nucleotide receptors and their ligands

✍ Scribed by Kenneth A. Jacobson; Hak Sung Kim; Gnana Ravi; Soo-Kyung Kim; Kyeong Lee; Aishe Chen; Wangzhong Chen; Seong Gon Kim; Dov Barak; Bruce T. Liang; Zhan-Guo Gao

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 143 KB
• Volume: 58
• Category: Article
• ISSN: 0272-4391
• DOI: 10.1002/ddr.10168

✦ Synopsis

Abstract

Modification of the ribose moiety of nucleotides and nucleosides has provided new insights into structural and conformational requirements for ligands at P2Y nucleotide receptors and at adenosine receptors (ARs). Methanocarba derivatives (containing a rigid bicyclic ring system in place of ribose) of adenosine, ATP, ADP, UTP, UDP, and other receptor agonist analogs were synthesized. Biological evaluation led to the conclusion that in general the Northern (N)‐conformation was favored over the Southern (S)‐conformation of the pseudoribose moiety at A~1~ and A~3~ ARs and at P2Y~1~, P2Y~2~, P2Y~4~, or P2Y~11~ receptors, but not P2Y~6~ receptors. At the hA~3~ AR a new full agonist, MRS1898, the (N)‐methanocarba equivalent of Cl‐IB‐MECA (2‐chloro‐N^6^‐(3‐iodobenzyl)‐5'‐N‐methylcarbamoyladenosine), had a K~i~ value of 1.9 nM in binding to the hA~3~ AR expressed in CHO cells. Functional assays confirmed the selectivity of MRS1898, although Cl‐IB‐MECA was even more functionally selective for human A~3~ vs. hA~1~ and hA~2A~ ARs. Thirty µM MRS1898 did not induce apoptosis in HL‐60 cells, suggesting that some of the proapoptotic effects of Cl‐IB‐MECA may be nonreceptor‐mediated. Manipulation of the sequence of A~3~ ARs through site‐directed mutagenesis has led to pharmacologically unique constructs: constitutively active receptors and “neoceptors.” Such engineered receptors may later prove to have potential for cardioprotection through gene transfer. Effects of single amino acid replacement were interpreted using a rhodopsin‐based model of ligand‐A~3~ receptor interactions, leading to the proposal that a movement of the conserved W243 in TM6 may be involved in AR activation. Drug Dev. Res. 58:330–339, 2003. © 2003 Wiley‐Liss, Inc.