Drugs interacting with G protein alpha subunits: selectivity and perspectives.
Fiche publication
Date publication
janvier 1998
Journal
Fundamental & clinical pharmacology
Auteurs
Membres identifiés du Cancéropôle Est :
Pr GIES Jean-Pierre, Dr DAEFFLER Laurent
Tous les auteurs :
Chahdi A, Daeffler L, Gies JP, Landry Y
Lien Pubmed
Résumé
Extracellular signal molecules as diverse as hormones, neurotransmitters and photons use a signal transduction pathway involving a receptor, a G protein and effectors. Compounds that interact directly with G proteins can mimic the receptor-G protein interaction or can block the activation of G proteins by receptors. Several binding sites exist on the G alpha protein that may be exploited for the design of synthetic stimulatory or inhibitory ligands. The effector binding site is regulated by endogenous proteins and appears to be a target for selective exogenous ligands. The GTP binding site presents a large homology within the G protein families and therefore the nucleotide analogs might not be considered as a tool to discriminate between the G protein subclasses. In contrast, different experimental strategies have substantiated the specificity in the interaction between a receptor and a G protein, the receptor binding site of G proteins should be considered as potential drug targets. Drugs interfering with this site such as mastoparan and related peptides, GPAnt-2 and suramin, are lead compounds in the design of selective G protein antagonists. Benzalkonium chloride and methoctramine have agonist or antagonist properties, depending on G protein subtypes. Such compounds would be very useful to delineate the functions of G proteins and G protein-coupled receptors, to understand some side effects of drugs used in therapy and to develop new therapeutic agents.
Mots clés
Amino Acid Sequence, Animals, Complement C3a, chemistry, GTP-Binding Protein alpha Subunits, Gs, agonists, Guanosine Triphosphate, metabolism, Hormones, chemistry, Humans, Molecular Sequence Data, Neuropeptides, metabolism, Neurotransmitter Agents, metabolism, Peptides, Polyamines, metabolism, Receptors, Drug, metabolism, Signal Transduction, physiology, Wasp Venoms, chemistry
Référence
Fundam Clin Pharmacol. 1998 ;12(2):121-32