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 AbstractStructure-activity relationships of the yeast alpha-factor    Next AbstractStudies on the yeast alpha-mating factor: a model for mammalian peptide hormones »

Biopolymers


Title:Synthetic probes for the alpha-factor receptor
Author(s):Naider F; Yaron A; Ewenson A; Tallon M; Xue CB; Srinivasan JV; Eriotou-Bargiota E; Becker JM;
Address:"Department of Chemistry, College of Staten Island, CUNY 10314"
Journal Title:Biopolymers
Year:1990
Volume:29
Issue:1
Page Number:237 - 245
DOI: 10.1002/bip.360290128
ISSN/ISBN:0006-3525 (Print) 0006-3525 (Linking)
Abstract:"The binding of the tridecapeptide yeast mating pheromone, alpha-factor, to its receptor represents an excellent model for the investigation of peptide hormone-receptor interactions. In this paper we present a number of strategies to probe the binding site of the alpha-factor receptor, and discuss the synthesis of probes containing radioactive and affinity tags. Preferential acylation of the alpha- or epsilon-amine in [Nle12]-alpha-factor was accomplished using 3-[3,5-diiodo-4-hydroxyphenyl] propanoic acid hydroxysuccinimide ester (diiodo Bolton-Hunter reagent). At pH 8.0 in a N-N-dimethylformamide/water mixture the ratio of epsilon- to alpha-acylation was 2.15 to 1, whereas at pH 6.5 in a 1,2-dimethoxyethane/water mixture alpha-acylation was favored by more than 3 to 1. The product distribution was found to depend on pH, organic cosolvent, and the ratio of organic solvent and aqueous buffer. Product distributions were followed using analytical high performance liquid chromatography and the products were characterized enzymatically and by mass spectrometry. Citraconic anhydride preferentially alpha-acylated [Nle12]-alpha-factor and served as a temporary masking group during the synthesis of epsilon-Bolton-Hunter acylated pheromone. Biotin or diiodo Bolton-Hunter reagents were also directly incorporated into [Nle12]-alpha-factor or Lys[Nle12]-alpha-factor during peptide synthesis. The peptides were assembled on a chloromethyl polystyrene resin or on a (phenylacetamido)methyl resin, and cleaved using anhydrous hydrogen fluoride (HF). Probes were inserted on amino groups either prior (biotin) or subsequent (Bolton-Hunter reagent) to HF cleavage. The biological activity of the synthetic peptides was characterized using growth arrest assays.(ABSTRACT TRUNCATED AT 250 WORDS)"
Keywords:"Amino Acid Sequence Binding Sites Hydrogen-Ion Concentration Mating Factor *Molecular Probes/chemical synthesis Molecular Sequence Data Peptides/*metabolism Pheromones/*metabolism Receptors, Cell Surface/*metabolism Receptors, Mating Factor *Receptors, Pe;"
Notes:"MedlineNaider, F Yaron, A Ewenson, A Tallon, M Xue, C B Srinivasan, J V Eriotou-Bargiota, E Becker, J M eng GM22086/GM/NIGMS NIH HHS/ GM22087/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1990/01/01 Biopolymers. 1990 Jan; 29(1):237-45. doi: 10.1002/bip.360290128"

 
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