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TitleStructural basis of odorant recognition by a human odorant receptor.
Journal, issue, pagesNature, Vol. 615, Issue 7953, Page 742-749, Year 2023
Publish dateMar 15, 2023
AuthorsChristian B Billesbølle / Claire A de March / Wijnand J C van der Velden / Ning Ma / Jeevan Tewari / Claudia Llinas Del Torrent / Linus Li / Bryan Faust / Nagarajan Vaidehi / Hiroaki Matsunami / Aashish Manglik /
PubMed AbstractOur sense of smell enables us to navigate a vast space of chemically diverse odour molecules. This task is accomplished by the combinatorial activation of approximately 400 odorant G protein-coupled ...Our sense of smell enables us to navigate a vast space of chemically diverse odour molecules. This task is accomplished by the combinatorial activation of approximately 400 odorant G protein-coupled receptors encoded in the human genome. How odorants are recognized by odorant receptors remains unclear. Here we provide mechanistic insight into how an odorant binds to a human odorant receptor. Using cryo-electron microscopy, we determined the structure of the active human odorant receptor OR51E2 bound to the fatty acid propionate. Propionate is bound within an occluded pocket in OR51E2 and makes specific contacts critical to receptor activation. Mutation of the odorant-binding pocket in OR51E2 alters the recognition spectrum for fatty acids of varying chain length, suggesting that odorant selectivity is controlled by tight packing interactions between an odorant and an odorant receptor. Molecular dynamics simulations demonstrate that propionate-induced conformational changes in extracellular loop 3 activate OR51E2. Together, our studies provide a high-resolution view of chemical recognition of an odorant by a vertebrate odorant receptor, providing insight into how this large family of G protein-coupled receptors enables our olfactory sense.
External linksNature / PubMed:36922591 / PubMed Central
MethodsEM (single particle)
Resolution3.1 - 3.2 Å
Structure data

EMDB-28896, PDB-8f76:
Human olfactory receptor OR51E2 bound to propionate in complex with miniGs399
Method: EM (single particle) / Resolution: 3.1 Å

EMDB-28900: Propionate bound to human olfactory receptor OR51E2 in complex with miniGs399 (transmembrane domain)
Method: EM (single particle) / Resolution: 3.2 Å

Chemicals

ChemComp-PPI:
PROPANOIC ACID / Propionic acid

Source
  • homo sapiens (human)
  • lama glama (llama)
KeywordsMEMBRANE PROTEIN / Human olfactory receptor / G protein-coupled receptor / odorant-binding / sensory transduction

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