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
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
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.