Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractFresh knowledge for an old relationship: new discoveries in molecular mycorrhizal research    Next AbstractInsect pheromone olfaction: new targets for the design of species-selective pest control agents »

Biochemistry


Title:Discrimination of pheromone enantiomers by two pheromone binding proteins from the gypsy moth Lymantria dispar
Author(s):Plettner E; Lazar J; Prestwich EG; Prestwich GD;
Address:"Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, British Columbia V5A 1S6, Canada"
Journal Title:Biochemistry
Year:2000
Volume:39
Issue:30
Page Number:8953 - 8962
DOI: 10.1021/bi000461x
ISSN/ISBN:0006-2960 (Print) 0006-2960 (Linking)
Abstract:"The gypsy moth, Lymantria dispar, uses (7R, 8S)-cis-2-methyl-7, 8-epoxyoctadecane, (+)-disparlure, as a sex pheromone. The (-) enantiomer of the pheromone is a strong behavioral antagonist. Specialized sensory hairs, sensillae, on the antennae of male moths detect the pheromone. Once the pheromone enters a sensillum, the very abundant pheromone binding protein (PBP) transports the odorant to the sensory neuron. We have expressed the two PBPs found in gypsy moth antennae, PBP1 and PBP2, and we have studied the affinity of these recombinant PBPs for the enantiomers of disparlure. To study pheromone binding under equilibrium conditions, we developed and validated a binding assay. We have addressed the two major problems with hydrophobic ligands in aqueous solution: (1) concentration-dependent adsorption of the ligand on vial surfaces and (2) separation of the protein-bound ligand from the material remaining free in solution. We used this assay to demonstrate for the first time that pheromone binding to PBP is reversible and that the two PBPs from L. dispar differ in their enantiomer binding preference. PBP1 has a higher affinity for the (-) enantiomer, while PBP2 has a higher affinity for the (+) enantiomer. The PBP from the wild silk moth, Antheraea polyphemus (Apol-3) bound the disparlure enantiomers more weakly than either of the L. dispar PBPs, but Apol-3 was also able to discriminate the enantiomers. We have observed extensive aggregation of both L. dispar PBPs and an increase in pheromone binding at high (>2 microM) PBP concentrations. We present a model of disparlure binding to the two PBPs"
Keywords:Alkanes/*metabolism Amino Acid Sequence Animals Carrier Proteins/genetics/*metabolism Insect Proteins/genetics/*metabolism Kinetics Molecular Sequence Data Moths/*metabolism Pheromones/*metabolism Recombinant Proteins/genetics/metabolism Sequence Homology;
Notes:"MedlinePlettner, E Lazar, J Prestwich, E G Prestwich, G D eng Comparative Study Research Support, U.S. Gov't, Non-P.H.S. 2000/07/29 Biochemistry. 2000 Aug 1; 39(30):8953-62. doi: 10.1021/bi000461x"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-06-2024