Title

Site-directed mutagenesis of P2U purinoceptors: Positively charged amino acids in transmembrane helices 6 and 7 affect agonist potency and specificity

Abstract

Two subtypes of G protein-coupled receptors for nucleotides (P and P purinoreceptors) contain several conserved positively charged amino acids in the third, sixth, and seventh putative transmembrane helices (TMHs). Since the fully ionized form of nucleotides has been shown to be an activating ligand for both P and P purinoceptors (P R and P R), we postulated that some of these positively charged amino acids are involved in binding of the negatively charged phosphate groups of nucleotides. To investigate the role of the conserved positively charged amino acids in purinoceptor function, a series of mutant P R cDNAs were constructed so that lysine 107 and arginine 110 in TMH 3, histidine 262 and arginine 265 in TMH 6, and arginine 292 in TMH 7 were changed to the neutral amino acid leucine or isoleucine. The mutated P R cDNAs were stably expressed in 1321N1 astrocytoma cells and receptor activity was monitored by quantitating changes in the concentration of intracellular Ca upon stimulation with full (ATP, UTP) or partial (ADP, UDP) P R agonists. Neutralization of His , Arg , or Arg caused a 100-850-fold decrease in the potency of ATP and UTP relative to the unmutated P R and rendered ADP and UDP ineffective. In contrast, neutralization of Lys or Arg did not alter the agonist potency or specificity of the P R. Neutralization of Lys in the P R, which is expressed as a glutamine residue in the P subtype, did not alter receptor activity; however, a conservative change from lysine to arginine at this position altered the rank order of agonist potency so that ADP and UDP were approximately 100-fold more potent than ATP and UTP. A three-dimensional model of the P R indicates the feasibility of His , Arg , and Arg interactions with the phosphate groups of nucleotides. 2U 2Y 2U 2Y 2U 2Y 2U 2U 2U 2U 2U 2U 2Y 2U 2+ 262 265 292 107 110 289 262 265 292

Document Type

Article

DOI

https://doi.org/10.1074/jbc.270.9.4185

Publication Date

3-3-1995

Journal Title

Journal of Biological Chemistry

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