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Molecular determinants of allosteric modulation at the M1 muscarinic acetylcholine receptor

Abdul-Ridha, Alaa; López, Laura; Keov, Peter; Thal, David M.; Mistry, Shailesh N.; Sexton, Patrick M.; Lane, J. Robert; Canals, Meritxell; Christopoulos, Arthur

Authors

Alaa Abdul-Ridha

Laura López

Peter Keov

David M. Thal

Patrick M. Sexton

ROB LANE ROB.LANE@NOTTINGHAM.AC.UK
Associate Professor

Arthur Christopoulos



Abstract

Benzylquinolone carboxylic acid (BQCA) is an unprecedented example of a selective positive allosteric modulator of acetylcholine at the M1 muscarinic acetylcholine receptor (mAChR). To probe the structural basis underlying its selectivity, we utilized site-directed mutagenesis, analytical modeling, and molecular dynamics to delineate regions of the M1 mAChR that govern modulator binding and transmission of cooperativity. We identified Tyr-852.64 in transmembrane domain 2 (TMII), Tyr-179 and Phe-182 in the second extracellular loop (ECL2), and Glu-3977.32 and Trp-4007.35 in TMVII as residues that contribute to the BQCA binding pocket at the M1 mAChR, as well as to the transmission of cooperativity with the orthosteric agonist carbachol. As such, the BQCA binding pocket partially overlaps with the previously described "common" allosteric site in the extracellular vestibule of the M1 mAChR, suggesting that its high subtype selectivity derives from either additional contacts outside this region or through a subtype-specific cooperativity mechanism. Mutation of amino acid residues that form the orthosteric binding pocket caused a loss of carbachol response that could be rescued by BQCA. Two of these residues (Leu-1023.29 and Asp-1053.32) were also identified as indirect contributors to the binding affinity of the modulator. This new insight into the structural basis of binding and function of BQCA can guide the design of new allosteric ligands with tailored pharmacological properties. © 2014 by The American Society for Biochemistry and Molecular Biology, Inc.

Citation

Abdul-Ridha, A., López, L., Keov, P., Thal, D. M., Mistry, S. N., Sexton, P. M., …Christopoulos, A. (2014). Molecular determinants of allosteric modulation at the M1 muscarinic acetylcholine receptor. Journal of Biological Chemistry, 289(9), 6067-6079. https://doi.org/10.1074/jbc.M113.539080

Journal Article Type Article
Acceptance Date Jan 16, 2014
Online Publication Date Jan 17, 2014
Publication Date Feb 28, 2014
Deposit Date Oct 9, 2015
Publicly Available Date Oct 9, 2015
Journal Journal of Biological Chemistry
Electronic ISSN 0021-9258
Publisher American Society for Biochemistry and Molecular Biology
Peer Reviewed Peer Reviewed
Volume 289
Issue 9
Pages 6067-6079
DOI https://doi.org/10.1074/jbc.M113.539080
Keywords Allosteric modulation; Molecular determinants; Muscarinic acetylcholine receptors; Muscarinic acetylcholine receptors (machr); Pharmacological properties; Positive allosteric modulator; Site directed mutagenesis; Trans-membrane domains; Activation analysi
Public URL http://eprints.nottingham.ac.uk/id/eprint/30415
Publisher URL http://www.jbc.org/content/289/9/6067
Copyright Statement Copyright information regarding this work can be found at the following address: http://eprints.nottingh.../end_user_agreement.pdf
Additional Information This research was originally published in Journal of Biological Chemistry. Alaa Abdul-Ridha, Laura López, Peter Keov, David M. Thal, Shailesh N. Mistry, Patrick M. Sexton, Meritxell Canals and Arthur Christopoulos. Molecular determinants of allosteric modulation at the M1 muscarinic acetylcholine receptor. Journal of Biological Chemistry. 2014. 289:6067-6079. © the American Society for Biochemistry and Molecular Biology.

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Copyright Statement
Copyright information regarding this work can be found at the following address: http://eprints.nottingham.ac.uk/end_user_agreement.pdf





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