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 AbstractPotential application of electronic olfaction systems in feedstuffs analysis and animal nutrition    Next AbstractRevisiting the specificity of Mamestra brassicae and Antheraea polyphemus pheromone-binding proteins with a fluorescence binding assay »

Eur J Biochem


Title:Recombinant pheromone binding protein 1 from Mamestra brassicae (MbraPBP1). Functional and structural characterization
Author(s):Campanacci V; Longhi S; Nagnan-Le Meillour P; Cambillau C; Tegoni M;
Address:"AFMB, UPR 9039-CNRS, Marseille, France"
Journal Title:Eur J Biochem
Year:1999
Volume:264
Issue:3
Page Number:707 - 716
DOI: 10.1046/j.1432-1327.1999.00666.x
ISSN/ISBN:0014-2956 (Print) 0014-2956 (Linking)
Abstract:"Pheromone binding proteins (PBPs) are small proteins (17 kDa on average) present at high concentrations ( approximately 10 mM) in the sensillum lymph of Lepidoptera antennae, where they play a key role in the perception of pheromones. By expression in Escherichia coli, we have obtained large quantities (2-3 mg.L-1) of pure, soluble, Mamestra brassicae PBP1 (MbraPBP1). These quantities are compatible with the requirements of X-ray and NMR studies. The recombinant protein has been characterized by native-polyacrylamide gel electrophoresis, Western blotting, N-terminal sequencing, mass spectrometry, gel filtration, circular dichroism, and NMR. Moreover, the recombinant MbraPBP1 has been shown to be able to bind the specific pheromone and a structural analogue, Z11-16:TFMK (cis-11-hexadecenyl trifluoromethyl ketone), in displacement experiments. Our results on MbraPBP1 confirm and extend previous findings on PBPs. MbraPBP1 and two PBPs from different species have been found to exist as dimers under nondenaturing conditions. The CD and structural prediction data confirm a markedly helical structure for insect PBPs rather than the beta-barrel fold found in vertebrates odorant binding proteins. We have tentatively identified the location of the helices and the short beta-strands with respect to the binding site. Currently we have obtained small diffracting crystals of the recombinant MbraPBP1 and determined their space group and molecular content"
Keywords:"Amino Acid Sequence Animals Base Sequence Carrier Proteins/*chemistry/genetics/*metabolism Circular Dichroism Crystallization DNA Primers/genetics Escherichia coli/genetics Gene Expression Genes, Insect Insect Proteins/*chemistry/genetics/*metabolism Lepi;"
Notes:"MedlineCampanacci, V Longhi, S Nagnan-Le Meillour, P Cambillau, C Tegoni, M eng England 1999/09/22 Eur J Biochem. 1999 Sep; 264(3):707-16. doi: 10.1046/j.1432-1327.1999.00666.x"

 
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 26-12-2024