Ostrinia furnacalis PBP2 solution NMR structure: Insight into ligand binding and release mechanisms.


Journal

Protein science : a publication of the Protein Society
ISSN: 1469-896X
Titre abrégé: Protein Sci
Pays: United States
ID NLM: 9211750

Informations de publication

Date de publication:
10 2022
Historique:
revised: 22 08 2022
received: 18 04 2022
accepted: 28 08 2022
entrez: 29 9 2022
pubmed: 30 9 2022
medline: 1 10 2022
Statut: ppublish

Résumé

Ostrinia furnacalis is an invasive lepidopteran agricultural pest that relies on olfaction for mating and reproduction. Male moths have an extremely sensitive olfactory system that can detect the sex pheromones emitted by females over a great distance. Pheromone-binding proteins present in the male moth antenna play a key role in the pheromone uptake, transport, and release at the dendritic membrane of the olfactory neuron. Here, we report the first high-resolution NMR structure of a pheromone-binding protein from an Ostrinia species at pH 6.5. The core of the Ostrinia furnacalis PBP2 (OfurPBP2) consists of six helices, α1a (2-14), α1b (16-22), α2 (27-37), α3 (46-60), α4 (70-80), α5 (84-100), and α6 (107-124) surrounding a large hydrophobic pocket. The structure is stabilized by three disulfide bridges, 19-54, 50-108, and 97-117. In contrast to the unstructured C-terminus of other lepidopteran PBPs, the C-terminus of OfurPBP2 folds into an α-helix (α7) at pH 6.5. The protein has nanomolar affinity towards both pheromone isomers. Molecular docking of both pheromones, E-12 and Z-12-tetradecenyl acetate, to OfurPBP2 revealed that the residues Met5, Lys6, Met8, Thr9, Phe12, Phe36, Trp37, Phe76, Ser115, Phe118, Lys119, Ile122, His123, and Ala128 interact with both isomers, while Thr9 formed a hydrogen bond with the acetate head group. NMR structure and thermal unfolding studies with CD suggest that ligand release at pH 4.5 is likely due to the partial unfolding of the protein.

Identifiants

pubmed: 36173163
doi: 10.1002/pro.4438
pmc: PMC9514217
doi:

Substances chimiques

Carrier Proteins 0
Disulfides 0
Insect Proteins 0
Ligands 0
Pheromones 0
Sex Attractants 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e4438

Informations de copyright

© 2022 The Protein Society.

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Auteurs

Salik R Dahal (SR)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

Jacob L Lewellen (JL)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

Shine Ayyappan (S)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

Bharat P Chaudhary (BP)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

Viswanath Nukala (V)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

Smita Mohanty (S)

Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma, USA.

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Classifications MeSH