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. 2018 Oct;94(4):1232-1245.
doi: 10.1124/mol.118.112649. Epub 2018 Aug 15.

Intracellular Binding Site for a Positive Allosteric Modulator of the Dopamine D1 Receptor

Xushan Wang  1 , Beverly A Heinz  2 , Yue-Wei Qian  1 , Joan H Carter  1 , Robert A Gadski  1 , Lisa S Beavers  1 , Sheila P Little  1 , Charles R Yang  1 , James P Beck  1 , Junliang Hao  1 , John M Schaus  1 , Kjell A Svensson  1 , Robert F Bruns  1
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Free article

Intracellular Binding Site for a Positive Allosteric Modulator of the Dopamine D1 Receptor

Xushan Wang et al. Mol Pharmacol. 2018 Oct.
Free article

Abstract

The binding site for DETQ [2-(2,6-dichlorophenyl)-1-((1S,3R)-3-(hydroxymethyl)-5-(2-hydroxypropan-2-yl)-1-methyl-3,4-dihydroisoquinolin-2(1H)-yl)ethan-1-one], a positive allosteric modulator (PAM) of the dopamine D1 receptor, was identified and compared with the binding site for CID 2886111 [N-(6-tert-butyl-3-carbamoyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)pyridine-4-carboxamide], a reference D1 PAM. From D1/D5 chimeras, the site responsible for potentiation by DETQ of the increase in cAMP in response to dopamine was narrowed down to the N-terminal intracellular quadrant of the receptor; arginine-130 in intracellular loop 2 (IC2) was then identified as a critical amino acid based on a human/rat species difference. Confirming the importance of IC2, a β2-adrenergic receptor construct in which the IC2 region was replaced with its D1 counterpart gained the ability to respond to DETQ. A homology model was built from the agonist-state β2-receptor structure, and DETQ was found to dock to a cleft created by IC2 and adjacent portions of transmembrane helices 3 and 4 (TM3 and TM4). When residues modeled as pointing into the cleft were mutated to alanine, large reductions in the potency of DETQ were found for Val119 and Trp123 (flanking the conserved DRY sequence in TM3), Arg130 (located in IC2), and Leu143 (TM4). The D1/D5 difference was found to reside in Ala139; changing this residue to methionine as in the D5 receptor reduced the potency of DETQ by approximately 1000-fold. None of these mutations affected the activity of CID 2886111, indicating that it binds to a different allosteric site. When combined, DETQ and CID 2886111 elicited a supra-additive response in the absence of dopamine, implying that both PAMs can bind to the D1 receptor simultaneously.

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