Disrupting Pheromone Signaling in Insects: Design, Synthesis, and Evaluation of an Inhibitor

Sex pheromones mediate mate recognition in insects through interactions with pheromone-binding proteins (PBPs). Targeting this pathway with pheromone analogs offers a species-specific approach to pest management. Here, we report the design, synthesis, and evaluation of a pheromone analog, (6<i>E</i>,11<i>Z</i>)-heptadeca-6,11-dien-1-yl acetate as an inhibitor of <i>Antheraea polyphemus</i> PBP1 (ApolPBP1). Molecular docking predicted potential binding orientations and interactions within the pocket. Fluorescence-based binding assays revealed a 4-fold higher dissociation constant, and 2D [<sup>1</sup>H, <sup>15</sup>N] HSQC NMR titrations confirmed reduced affinity, with ApolPBP1 transitioning to the bound state only at higher analog concentrations. Overall, these findings highlight the sensitivity of PBPs to subtle structural modifications in their ligands and emphasize the importance of preserving key molecular interactions for effective binding.

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Publication Details

Journal
ACS Omega
Published
2026-01-16
DOI
https://doi.org/10.1021/acsomega.5c06376
Citations
1
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
23.21
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article

Disrupting Pheromone Signaling in Insects: Design, Synthesis, and Evaluation of an Inhibitor

Sarah R. Moor, James R. Howard, Eric V. Anslyn, Smita Mohanty et al.
1 citations
ACS Omega
Neurobiology and Insect Physiology Research
23.21
article

Disrupting Pheromone Signaling in Insects: Design, Synthesis, and Evaluation of an Inhibitor

Sarah R. Moor, James R. Howard, Eric V. Anslyn, Smita Mohanty, Anna Lidskog, Josef M. Maier, Pratikshya Paudel, Ishani Ray, Omar Al Danoon
article en
1 citations

Abstract

Sex pheromones mediate mate recognition in insects through interactions with pheromone-binding proteins (PBPs). Targeting this pathway with pheromone analogs offers a species-specific approach to pest management. Here, we report the design, synthesis, and evaluation of a pheromone analog, (6<i>E</i>,11<i>Z</i>)-heptadeca-6,11-dien-1-yl acetate as an inhibitor of <i>Antheraea polyphemus</i> PBP1 (ApolPBP1). Molecular docking predicted potential binding orientations and interactions within the pocket. Fluorescence-based binding assays revealed a 4-fold higher dissociation constant, and 2D [<sup>1</sup>H, <sup>15</sup>N] HSQC NMR titrations confirmed reduced affinity, with ApolPBP1 transitioning to the bound state only at higher analog concentrations. Overall, these findings highlight the sensitivity of PBPs to subtle structural modifications in their ligands and emphasize the importance of preserving key molecular interactions for effective binding.

ACS OmegaVol. 11(8)
Oklahoma State University Oklahoma City (US), The University of Texas at Austin (US)
Zero hunger
Openalex Percentile: Top 3%
Neurobiology and Insect Physiology Research
23.21
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Disrupting Pheromone Signaling in Insects: Design, Synthesis, and Evaluation of an Inhibitor — Sarah R. Moor, James R. Howard, et al. · ACS Omega (2026) | TGRS Research Map | TGRS