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 AbstractSize-resolved gas-particle partitioning characteristics of typical semi-volatile organic compounds in urban atmosphere    Next Abstract"A study of the reactions of H3O+, NO+ and O2+ ions with nine alkoxy alcohols" »

Insect Mol Biol


Title:"Specific involvement of two amino acid residues in cis-nerolidol binding to odorant-binding protein 5 AlinOBP5 in the alfalfa plant bug, Adelphocoris lineolatus (Goeze)"
Author(s):Wang SY; Gu SH; Han L; Guo YY; Zhou JJ; Zhang YJ;
Address:"State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China"
Journal Title:Insect Mol Biol
Year:2013
Volume:20130107
Issue:2
Page Number:172 - 182
DOI: 10.1111/imb.12012
ISSN/ISBN:1365-2583 (Electronic) 0962-1075 (Linking)
Abstract:"Olfaction plays an important role in insects' survival and reproduction. Odorant-binding proteins (OBPs) are considered to be one of the crucial proteins in the insect olfactory pathway. In this study, an antenna-specific OBP of the alfalfa plant bug, Adelphocoris lineolatus AlinOBP5, was expressed and purified in vitro. The binding affinities of AlinOBP5 with sex pheromone analogues of the Miridae and cotton volatiles were investigated by fluorescence competitive binding assays. The binding sites of AlinOBP5 were predicted by three-dimensional structure modelling and molecular docking, and site-directed mutagenesis. AlinOBP5 could not effectively bind with sex pheromone analogues of Miridae but showed high binding abilities with specific cotton volatiles, such as cis-nerolidol, ethyl laurate, beta-ionone, beta-caryophyllene, 2,3-dimethylbenzoic acid and (E)-farnesol. The strongest binding affinity was to cis-nerolidol, suggesting a role of AlinOBP5 in general odorant chemoreception. Based on the relatively strong binding affinity and the reported physiological activity of cis-nerolidol in other insects, we chose cis-nerolidol for further homology modelling and ligand docking. The results of molecular simulation and site-directed mutagenesis indicated that two amino acids, Lys74 and Pro121, in the protein binding pocket are the key amino acids involved in the binding of cis-nerolidol. The Lys74 residue may participate in specific recognition of ligands, and the Pro121 residue plays a crucial role in ligand binding and release by changing the binding pocket environment and stabilizing the conformation of the C-terminus of AlinOBP5"
Keywords:"Amino Acid Sequence Animals Binding Sites Cloning, Molecular Fluorescence Gossypium/metabolism Heteroptera/*physiology Insect Proteins/*chemistry/genetics/*metabolism Ligands Lysine/chemistry/metabolism Medicago sativa Molecular Docking Simulation Molecul;"
Notes:"MedlineWang, S-Y Gu, S-H Han, L Guo, Y-Y Zhou, J-J Zhang, Y-J eng Research Support, Non-U.S. Gov't England 2013/01/09 Insect Mol Biol. 2013 Apr; 22(2):172-82. doi: 10.1111/imb.12012. Epub 2013 Jan 7"

 
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 17-11-2024