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 AbstractGenetic Dissection of Sexual Reproduction in a Primary Homothallic Basidiomycete    Next AbstractInvolvement of thermophilic archaea in the biocorrosion of oil pipelines »

J Biol Chem


Title:"Expression and purification of the Saccharomyces cerevisiae alpha-factor receptor (Ste2p), a 7-transmembrane-segment G protein-coupled receptor"
Author(s):David NE; Gee M; Andersen B; Naider F; Thorner J; Stevens RC;
Address:"Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, California 94720, USA"
Journal Title:J Biol Chem
Year:1997
Volume:272
Issue:24
Page Number:15553 - 15561
DOI: 10.1074/jbc.272.24.15553
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"A plasmid vector was developed that permitted high-level expression of a functional form of the Saccharomyces cerevisiae alpha-factor receptor (the STE2 gene product) tagged at its C-terminal end with an epitope (FLAG) and a His6 tract. When expressed in yeast from this plasmid, Ste2p was produced at a level at least 3-fold higher than that reported previously for any other 7-transmembrane-segment receptor expressed in the same cells. For purification, isolated cell membranes containing the overexpressed receptor were solubilized with detergent under specific conditions and subjected to immobilized metal affinity chromatography. Yields as high as 1 mg of nearly homogeneous (95%) receptor were routinely obtained even from relatively small scale preparations (60 g of frozen cell paste). The purified receptor was reconstituted into artificial phospholipid vesicles. Radioligand binding studies demonstrated that the purified receptor, in the reconstituted vesicles, bound its tridecapeptide ligand (alpha-factor) with a KD (155 nM) consistent with the affinity expected for this receptor in the absence of its associated G protein. Efficient restoration of ligand binding activity upon reconstitution required the addition of solubilized membranes prepared from a yeast strain lacking the receptor. Sufficient amounts of active material can be obtained by this procedure to allow physical studies of this receptor and other 7-transmembrane-segment receptors expressed in this system"
Keywords:"Amino Acid Sequence Base Sequence Cloning, Molecular DNA, Recombinant GTP-Binding Proteins/metabolism Mating Factor Molecular Sequence Data Peptides/metabolism Plasmids Radioligand Assay Receptors, Mating Factor Receptors, Peptide/*genetics/isolation & pu;"
Notes:"MedlineDavid, N E Gee, M Andersen, B Naider, F Thorner, J Stevens, R C eng GM07232/GM/NIGMS NIH HHS/ GM22086/GM/NIGMS NIH HHS/ GM22087/GM/NIGMS NIH HHS/ etc. Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1997/06/13 J Biol Chem. 1997 Jun 13; 272(24):15553-61. doi: 10.1074/jbc.272.24.15553"

 
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 29-12-2024