N. Blin et al., MAPPING OF SINGLE AMINO-ACID-RESIDUES REQUIRED FOR SELECTIVE ACTIVATION OF G(Q 11) BY THE M3 MUSCARINIC ACETYLCHOLINE-RECEPTOR/, The Journal of biological chemistry, 270(30), 1995, pp. 17741-17748
Each G protein coupled receptor can interact only with a limited numbe
r of the many structurally similar G proteins expressed within a cell.
This study was undertaken to identify single amino acids required for
selectively coupling the m3 muscarinic acetylcholine receptor to G pr
oteins of the G(q/11) family. To this goal, distinct intracellular seg
ments/amino acids of the m3 receptor were systematically substituted i
nto the structurally closely related m2 muscarinic receptor, which cou
ples to G(i/o) proteins, not G(q/11) proteins. The resultant mutant re
ceptors were expressed in COS-7 cells and studied for their ability to
induce agonist-dependent stimulation of phosphatidylinositol hydrolys
is, a response known to be mediated by G proteins of the G(q/11) class
. Using this approach, we were able to identify four amino acids in th
e second intracellular loop and four amino acids at the C terminus of
the third intracellular loop of the m3 muscarinic receptor that are es
sential for efficient G(q/11) activation. We could demonstrate that th
ese amino acids, together with a short segment at the N terminus of th
e third intracellular loop, fully account for the G protein coupling p
reference of the m3 muscarinic receptor. Taken together, our data stro
ngly suggest that only a limited number of amino acids, located on dif
ferent intracellular regions, are required to determine the functional
profile of a given G protein-coupled receptor.