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J. Biol. Chem., Vol. 269, Issue 45, 27900-27906, Nov, 1994
AL Tucker, AS Robeva, HE Taylor, D Holeton, M Bockner, KR Lynch and J Linden
Species differences in ligand binding to A1 adenosine receptors were
localized to the seventh transmembrane (TM7) region based on the binding of
[8-3H]cyclopentyl-1, 3-dipropylxanthine and three other ligands to wild
type and six bovine/canine interspecies receptor chimeras expressed in
COS-1 cells. Subsequent site-directed mutagenesis experiments identified
amino acid 270 (isoleucine/methionine, bovine/canine) as being primarily
responsible for species differences in the binding of
N6-adenine-substituted compounds, R-N6- phenylisopropyladenosine (R-PIA)
and (S)-N6-endonorbornan-2-yl-9- methyladenine, and the C-8-substituted
xanthine, [3H]cyclopentyl-1,3- dipropylxanthine. These data are consistent
with the hypothesis that the N6 region of adenines and the C-8-region of
xanthines bind to the same region of the receptor. A second TM7 amino acid,
277 (serine/threonine, bovine/canine), selectively influences the binding
of the ribose-substituted adenosine analog, 5'-N- ethylcarboxamidoadenosine
to a variable extent, depending on the nature of amino acid 270. We
hypothesize that amino acid 270 of the A1 receptor interacts with the N6
region of adenosine, while amino acid 277 is important, especially in the
absence of an N6 substitution, for interactions with a distinct nucleoside
region, possibly on the ribose.
A1 adenosine receptors. Two amino acids are responsible for species differences in ligand recognition
Department of Internal Medicine, University of Virginia, Charlottesville 22908.
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