Affiliation: | * Department of Pharmacology, University of Michigan, M6322 Medical Science Bldg 1, Ann Arbor, MI 48109, U.S.A. † Department of Internal Medicine (Hypertension), University of Michigan, M6322 Medical Science Bldg 1, Ann Arbor, MI 48109, U.S.A. |
Abstract: | Triggered by agonist binding to cell surface receptors, the heterotrimeric G proteins dissociate into and βγ subunits, each activating distinct second messenger pathways. Peptides from the primary sequences of receptors, G proteins, and effectors have been used to study the molecular interactions between these proteins. Receptor-derived peptides from the second, third and fourth intracellular loops and certain naturally occurring peptides antagonize G protein interactions and can directly activate G protein. These peptides bind to G protein sites that include the N and C terminal regions of the subunit and a yet to be identified region of the β subunit. Peptides have also been useful in characterizing G protein-effector interactions. The identification of the contact sites between proteins involved in G protein signal transduction should aid in the development of non-peptide mimetic therapeutics which could specifically modify G protein-mediated cellular responses. |