The structural study of mutation-induced inactivation of human muscarinic receptor M4
Source abstract
Abstract
Human muscarinic receptor M4 belongs to the class A subfamily of the G-protein-coupled receptors (GPCRs). M4 has emerged as an attractive drug target for the treatment of Alzheimer's disease and schizophrenia. Recent results showed that M4-mediated cholinergic transmission is related to motor symptoms in Parkinson's disease. Selective ligand design for the five muscarinic acetylcholine receptor (mAchR) subtypes currently remains challenging owing to the high sequence and structural similarity of their orthosteric binding pockets. In order to obtain M4-selective antagonists, a new approach was tried to lock M4 into an inactive form by rationally designing an N4497.49R mutation, which mimics the allosteric sodium binding in the conserved sodium site usually found in class A GPCRs. In addition, the crystal structure of the mutation-induced inactive M4 was determined. By comparative analysis with other mAchR structures, followed by functional assays, the N4497.49R mutation was shown to stabilize M4 into an inactive state. Virtual screening of a focused ligand library using the crystal structure showed that the inactive M4 prefers antagonists much more than agonists. This study provides a powerful mutation strategy to stabilize GPCRs in inactive states and facilitate their structure determination.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Receptor Mechanisms and Signaling · Monoclonal and Polyclonal Antibodies Research · Mass Spectrometry Techniques and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (55)
Show source-provided references
1. Alexandrov · Structure · 2008 · 16 · 35110.1016/j.str.2008.02.004 ↗
2. Ballesteros · Methods Neurosci. · 1995 · 25 · 36610.1016/S1043-9471(05)80049-7 ↗
3. Bernard · J. Neurosci. · 1992 · 12 · 359110.1523/JNEUROSCI.12-09-03591.1992 ↗
4. Bois · J. Chem. Neuroanat. · 2005 · 29 · 28210.1016/j.jchemneu.2005.03.005 ↗
5. Burger · J. Gen. Physiol. · 2018 · 150 · 136010.1085/jgp.201711979 ↗
6. Caffrey · Nat. Protoc. · 2009 · 4 · 70610.1038/nprot.2009.31 ↗
7. Chan · Proc. Natl Acad. Sci. USA · 2008 · 105 · 1097810.1073/pnas.0800567105 ↗
8. Chen · Acta Cryst. D · 2010 · 66 · 1210.1107/S0907444909042073 ↗
9. Darden · J. Chem. Phys. · 1993 · 98 · 1008910.1063/1.464397 ↗
10. Eglen · Handb. Exp. Pharmacol. · 2012 · 208 · 310.1007/978-3-642-23274-9_1 ↗
11. Eglen · Pharmacol. Rev. · 1996 · 48 · 531
12. Emsley · Acta Cryst. D · 2010 · 66 · 48610.1107/S0907444910007493 ↗
13. Eskow Jaunarajs · Prog. Neurobiol. · 2015 · 127-128 · 9110.1016/j.pneurobio.2015.02.002 ↗
14. Farkas · Brain Res. · 2002 · 954 · 3210.1016/S0006-8993(02)03300-0 ↗
15. Fenalti · Nature · 2014 · 506 · 19110.1038/nature12944 ↗
16. Flynn · Synapse · 1993 · 14 · 28310.1002/syn.890140406 ↗
17. Fredriksson · Mol. Pharmacol. · 2003 · 63 · 125610.1124/mol.63.6.1256 ↗
18. Freund · Exp. Gerontol. · 1986 · 21 · 3710.1016/0531-5565(86)90016-1 ↗
19. Haga · Nature · 2012 · 482 · 54710.1038/nature10753 ↗
20. Horcajada · J. Biol. Chem. · 2006 · 281 · 292310.1074/jbc.M507394200 ↗
21. Huang · Nature · 2015 · 524 · 31510.1038/nature14886 ↗
22. Hulme · Annu. Rev. Pharmacol. Toxicol. · 1990 · 30 · 63310.1146/annurev.pa.30.040190.003221 ↗
23. Humphrey · J. Mol. Graph. · 1996 · 14 · 3310.1016/0263-7855(96)00018-5 ↗
24. Jo · J. Comput. Chem. · 2008 · 29 · 185910.1002/jcc.20945 ↗
25. Kabsch · Acta Cryst. D · 2010 · 66 · 12510.1107/S0907444909047337 ↗
26. Karplus · Science · 2012 · 336 · 103010.1126/science.1218231 ↗
27. Kato · Circ. J. · 2006 · 70 · 165810.1253/circj.70.1658 ↗
28. Katritch · Trends Biochem. Sci. · 2014 · 39 · 23310.1016/j.tibs.2014.03.002 ↗
29. Kruse · Nature · 2012 · 482 · 55210.1038/nature10867 ↗
30. Kruse · Nature · 2013 · 504 · 10110.1038/nature12735 ↗
31. Lam · J. Optom. · 2010 · 3 · 3710.3921/joptom.2010.37 ↗
32. Liebschner · Acta Cryst. D · 2019 · 75 · 86110.1107/S2059798319011471 ↗
33. Liu · Proc. Natl Acad. Sci. USA · 2018 · 115 · 1204610.1073/pnas.1813988115 ↗
34. Liu · Science · 2012 · 337 · 23210.1126/science.1219218 ↗
35. Lomize · Nucleic Acids Res. · 2012 · 40 · D37010.1093/nar/gkr703 ↗
36. Maeda · Science · 2019 · 364 · 55210.1126/science.aaw5188 ↗
37. Maier · J. Chem. Theory Comput. · 2015 · 11 · 369610.1021/acs.jctc.5b00255 ↗
38. McCoy · J. Appl. Cryst. · 2007 · 40 · 65810.1107/S0021889807021206 ↗
39. Miller-Gallacher · PLoS One · 2014 · 9 · e9272710.1371/journal.pone.0092727 ↗
40. Peng · Cell · 2018 · 172 · 71910.1016/j.cell.2018.01.001 ↗
41. Popov · Curr. Opin. Struct. Biol. · 2019 · 55 · 2510.1016/j.sbi.2019.02.010 ↗
42. Popov · eLife · 2018 · 7 · e3472910.7554/eLife.34729 ↗
43. Roe · J. Chem. Theory Comput. · 2013 · 9 · 308410.1021/ct400341p ↗
44. Ryckaert · J. Comput. Phys. · 1977 · 23 · 32710.1016/0021-9991(77)90098-5 ↗
45. Smart · Acta Cryst. D · 2012 · 68 · 36810.1107/S0907444911056058 ↗
46. Suno · Nat. Chem. Biol. · 2018 · 14 · 115010.1038/s41589-018-0152-y ↗
47. Thal · Nature · 2016 · 531 · 33510.1038/nature17188 ↗
48. Vickery · Structure · 2018 · 26 · 17110.1016/j.str.2017.11.013 ↗
49. Wang · J. Comput. Chem. · 2004 · 25 · 115710.1002/jcc.20035 ↗
50. Winn · Acta Cryst. D · 2011 · 67 · 23510.1107/S0907444910045749 ↗
51. Yang · ACS Med. Chem. Lett. · 2019 · 10 · 94110.1021/acsmedchemlett.9b00106 ↗
52. Yazdani · J. Optom. · 2018 · 11 · 13510.1016/j.optom.2017.09.001 ↗
53. Yin · Nat. Struct. Mol. Biol. · 2016 · 23 · 29310.1038/nsmb.3183 ↗
54. Zhang · Nature · 2012 · 492 · 38710.1038/nature11701 ↗
55. Ztaou · J. Neurosci. · 2016 · 36 · 916110.1523/JNEUROSCI.0873-16.2016 ↗