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 AbstractCyclin B proteolysis and the cyclin-dependent kinase inhibitor rum1p are required for pheromone-induced G1 arrest in fission yeast    Next AbstractClassification and genetic targeting of cell types in the primary taste and premotor center of the adult Drosophila brain »

J Insect Physiol


Title:Molecular modeling of the binding of pheromone biosynthesis activating neuropeptide to its receptor
Author(s):Stern PS; Yu L; Choi MY; Jurenka RA; Becker L; Rafaeli A;
Address:"Chemical Physics Department, Weizmann Institute of Science, 76100 Rehovot, Israel"
Journal Title:J Insect Physiol
Year:2007
Volume:20070401
Issue:8
Page Number:803 - 818
DOI: 10.1016/j.jinsphys.2007.03.012
ISSN/ISBN:0022-1910 (Print) 0022-1910 (Linking)
Abstract:"Moth sex-pheromone biosynthesis follows a circadian cycle, which is cued by the release of the neurohormone pheromone biosynthesis activating neuropeptide (PBAN) to the hemolymph. PBAN binds to a G protein-coupled receptor (GPCR), in pheromone glands, (PG) initially identified by us in Helicoverpa zea moths (HezPBAN-R). In this study, the sequences of the seven transmembrane helices of HezPBAN-R were identified, built, packed and oriented correctly after multiple sequence alignment of the HezPBAN-R and several other GPCRs using the X-ray structure of rhodopsin as a template. Molecular dynamics simulations were run on three different beta-turn types of the C-terminal hexapeptide of PBAN and the results clustered into 12 structurally distinct groups. The lowest energy conformation from each group was used for computer-simulated docking with the model of the HezPBAN-R. Highest scoring complexes were examined and putative binding sites were identified. Experimental studies, using in vitro PG, revealed lower levels of pheromonotropic activity when challenged with pyrokinin-like peptides than with HezPBAN as ligand. Thus, the Drosophila melanogaster pyrokinin-1 receptor (CG9918) was chosen to create chimera receptors by exchanging between the three extracellular loops of the HezPBAN-R and the CG9918 for in silico mutagenesis experiments. The predicted docking model was validated with experimental data obtained from expressed chimera receptors in Sf9 cells"
Keywords:"Amino Acid Sequence Animals Binding Sites Models, Molecular Molecular Sequence Data Moths/*metabolism Neuropeptides/chemistry/*metabolism Protein Structure, Tertiary;"
Notes:"MedlineStern, Peter S Yu, Lian Choi, Man-Yeon Jurenka, Russell A Becker, Liron Rafaeli, Ada eng Research Support, Non-U.S. Gov't England 2007/05/22 J Insect Physiol. 2007 Aug; 53(8):803-18. doi: 10.1016/j.jinsphys.2007.03.012. Epub 2007 Apr 1"

 
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 24-12-2024