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Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds.

Publication ,  Journal Article
Ahmed, L; Zhang, Y; Block, E; Buehl, M; Corr, MJ; Cormanich, RA; Gundala, S; Matsunami, H; O'Hagan, D; Ozbil, M; Pan, Y; Sekharan, S; Ten, N ...
Published in: Proc Natl Acad Sci U S A
April 24, 2018

Understanding olfaction at the molecular level is challenging due to the lack of crystallographic models of odorant receptors (ORs). To better understand the molecular mechanism of OR activation, we focused on chiral (R)-muscone and other musk-smelling odorants due to their great importance and widespread use in perfumery and traditional medicine, as well as environmental concerns associated with bioaccumulation of musks with estrogenic/antiestrogenic properties. We experimentally and computationally examined the activation of human receptors OR5AN1 and OR1A1, recently identified as specifically responding to musk compounds. OR5AN1 responds at nanomolar concentrations to musk ketone and robustly to macrocyclic sulfoxides and fluorine-substituted macrocyclic ketones; OR1A1 responds only to nitromusks. Structural models of OR5AN1 and OR1A1 based on quantum mechanics/molecular mechanics (QM/MM) hybrid methods were validated through direct comparisons with activation profiles from site-directed mutagenesis experiments and analysis of binding energies for 35 musk-related odorants. The experimentally found chiral selectivity of OR5AN1 to (R)- over (S)-muscone was also computationally confirmed for muscone and fluorinated (R)-muscone analogs. Structural models show that OR5AN1, highly responsive to nitromusks over macrocyclic musks, stabilizes odorants by hydrogen bonding to Tyr260 of transmembrane α-helix 6 and hydrophobic interactions with surrounding aromatic residues Phe105, Phe194, and Phe207. The binding of OR1A1 to nitromusks is stabilized by hydrogen bonding to Tyr258 along with hydrophobic interactions with surrounding aromatic residues Tyr251 and Phe206. Hydrophobic/nonpolar and hydrogen bonding interactions contribute, respectively, 77% and 13% to the odorant binding affinities, as shown by an atom-based quantitative structure-activity relationship model.

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Published In

Proc Natl Acad Sci U S A

DOI

EISSN

1091-6490

Publication Date

April 24, 2018

Volume

115

Issue

17

Start / End Page

E3950 / E3958

Location

United States

Related Subject Headings

  • Receptors, Odorant
  • Protein Structure, Secondary
  • Protein Stability
  • Mutagenesis, Site-Directed
  • Models, Molecular
  • Hydrophobic and Hydrophilic Interactions
  • Hydrogen Bonding
  • Humans
  • HEK293 Cells
  • Cycloparaffins
 

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Ahmed, L., Zhang, Y., Block, E., Buehl, M., Corr, M. J., Cormanich, R. A., … Zhuang, H. (2018). Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds. Proc Natl Acad Sci U S A, 115(17), E3950–E3958. https://doi.org/10.1073/pnas.1713026115
Ahmed, Lucky, Yuetian Zhang, Eric Block, Michael Buehl, Michael J. Corr, Rodrigo A. Cormanich, Sivaji Gundala, et al. “Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds.Proc Natl Acad Sci U S A 115, no. 17 (April 24, 2018): E3950–58. https://doi.org/10.1073/pnas.1713026115.
Ahmed L, Zhang Y, Block E, Buehl M, Corr MJ, Cormanich RA, et al. Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds. Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):E3950–8.
Ahmed, Lucky, et al. “Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds.Proc Natl Acad Sci U S A, vol. 115, no. 17, Apr. 2018, pp. E3950–58. Pubmed, doi:10.1073/pnas.1713026115.
Ahmed L, Zhang Y, Block E, Buehl M, Corr MJ, Cormanich RA, Gundala S, Matsunami H, O’Hagan D, Ozbil M, Pan Y, Sekharan S, Ten N, Wang M, Yang M, Zhang Q, Zhang R, Batista VS, Zhuang H. Molecular mechanism of activation of human musk receptors OR5AN1 and OR1A1 by (R)-muscone and diverse other musk-smelling compounds. Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):E3950–E3958.
Journal cover image

Published In

Proc Natl Acad Sci U S A

DOI

EISSN

1091-6490

Publication Date

April 24, 2018

Volume

115

Issue

17

Start / End Page

E3950 / E3958

Location

United States

Related Subject Headings

  • Receptors, Odorant
  • Protein Structure, Secondary
  • Protein Stability
  • Mutagenesis, Site-Directed
  • Models, Molecular
  • Hydrophobic and Hydrophilic Interactions
  • Hydrogen Bonding
  • Humans
  • HEK293 Cells
  • Cycloparaffins