Comparative analysis of the efficacy of A(1) adenosine receptor activationof G(i)/(o)alpha G proteins following coexpression of receptor and c protein and expression of A(1) adenosine receptor-G(i/o alpha) fusion proteins

Citation
A. Wise et al., Comparative analysis of the efficacy of A(1) adenosine receptor activationof G(i)/(o)alpha G proteins following coexpression of receptor and c protein and expression of A(1) adenosine receptor-G(i/o alpha) fusion proteins, BIOCHEM, 38(8), 1999, pp. 2272-2278
Citations number
22
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMISTRY
ISSN journal
00062960 → ACNP
Volume
38
Issue
8
Year of publication
1999
Pages
2272 - 2278
Database
ISI
SICI code
0006-2960(19990223)38:8<2272:CAOTEO>2.0.ZU;2-C
Abstract
HEK293T cells were transiently transfected to express either the human A(1) adenosine receptor together with pertussis toxin-resistant cysteine-to-gly cine forms of the a subunits of G(i1) (C351G), G(i2) (C352G), and G(i3) (C3 51G) and wild-type G(o1)alpha or fusion proteins comprising the A(1) adenos ine receptor and these G(i/o) G proteins to compare A(1) adenosine receptor agonist-mediated activation of these G(i) family G proteins upon coexpress ion of individual G(i/o) G proteins and receptor versus expression as recep tor-G protein fusion proteins. Addition of the adenosine receptor agonist 5 '-N-ethylcarboxamidoadenosine (NECA) to membranes of pertussis toxin-treate d cells resulted in a concentration-dependent stimulation of [S-35]-GTP gam ma S binding with comparable amounts of NECA required to produce half-maxim al stimulation following transfection of A(1) adenosine receptor and G(i/o) G proteins either as fusion proteins or as separate polypeptides, However, the magnitude of agonist-mediated activation of GTP gamma S binding was gr eatly enhanced by expressing the A(1) adenosine receptor and G(i) family G proteins from chimaeric open reading frames. This observation was consisten t following the study of more than 40 agonists. Na preferential activation of any G protein was observed with more than 40 A(1) receptor agonists foll owing cotransfection of receptor with G protein or transfection of receptor -G protein fusion proteins. These studies demonstrate the utility of using fusion proteins to study receptor-G protein interaction, show that the A(1) adenosine receptor couples equally well to the G(i/o) G proteins G(i1)alph a, G(i2)alpha, G(i3)alpha, and G(o1)alpha, and demonstrate that for a range of agonists there is no selectivity for activation of any particular A(1) adenosine receptor-G(i/o) G protein combination.