Site-directed mutagenesis of the putative human muscarinic M 2 receptor binding site

• Published in: European journal of pharmacology Vol. 380; no. 2; pp. 183 - 195
• Main Authors: Heitz, Freddy, Holzwarth, James A, Gies, Jean-Pierre, Pruss, Rebecca M, Trumpp-Kallmeyer, Suzanne, Hibert, Marcel F, Guenet, Chantal
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 10.09.1999
• Subjects: G-protein coupled receptor; Human; Muscarinic M 2 receptor; Site-directed mutagenesis; Human; G-protein coupled receptor; Muscarinic M 2 receptor; Site-directed mutagenesis
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/S0014-2999(99)00439-2

Experimental probing of the model of the muscarinic M 2 receptor binding site proposed by Hibert et al. [Hibert, M.F., Trumpp-Kallmeyer, S., Bruinsvels, A., Hoflak, K., 1991. Three-dimensional models of neurotransmitter G-binding protein-coupled receptors. Mol. Pharmacol. 40, 8–15.] was achieved by mutating each amino-acid proposed to interact with muscarinic ligands. Pharmacological analysis of the different mutant receptors transiently expressed in human embryonic kidney (HEK/293) cells was performed with a variety of agonists and antagonists. D103A, Y403A and N404A mutations prevented binding of [ 3 H ] N-methylscopolamine and [ 3 H ] quinuclidinyl benzilate with a reduction in affinity greater than 100-fold, indicating essential contributions of these residues to the binding site for the radioligands. W400A and W155A mutations had very large effects on the binding of [ 3 H ] N-methylscopolamine (150-fold, 960-fold) but modest effects on the binding of [ 3 H ] quinuclidinyl benzilate (4-fold, 17-fold). In addition, binding of oxotremorine-M, oxotremorine, arecoline and pilocarpine to W155A resulted in a greater than 100-fold decrease in affinity. Threonine mutations (T187A and T190A) alter binding of most agonists but not of antagonists. W99 makes little contribution (<10-fold) to the binding site of the M 2 receptor. D103, W155, W400, Y403 and N404 are likely to be part of the binding site for N-methylscopolamine and also to contribute to the binding site for quinuclidinyl benzilate. Some of the predicted residues do not seem to be part of the M 2 receptor binding site but W155 is important for proper ligand binding on the muscarinic M 2 receptor, as predicted by the proposed model.