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 AbstractTranscription factor regulatory modules provide the molecular mechanisms for functional redundancy observed among transcription factors in yeast    Next AbstractReview on plant terpenoid emissions worldwide and in China »

Biochemistry


Title:Systematic analysis of the Saccharomyces cerevisiae alpha-factor containing lactam constraints of different ring size
Author(s):Yang W; McKinney A; Becker JM; Naider F;
Address:"Department of Chemistry, College of Staten Island, City University of New York 10314"
Journal Title:Biochemistry
Year:1995
Volume:34
Issue:4
Page Number:1308 - 1315
DOI: 10.1021/bi00004a025
ISSN/ISBN:0006-2960 (Print) 0006-2960 (Linking)
Abstract:"Eight cyclic analogs and corresponding linear homologs of the alpha-factor mating pheromone (WHWLQLKPGQPMY) of Saccharomyces cerevisiae were synthesized using solid-phase procedures on a phenylacetamidomethyl support. On-resin lactamization of the side chains of residues 7 and 10 to form rings containing from 14 to 18 atoms was effected by the BOP reagent. All peptides were highly homogeneous and gave expected molecular ions by FAB mass spectrometry. The constrained analogs had biological activities varying from 10% to less than 0.1% of that of [Nle12]-alpha-factor. In all cases, cyclic analogs with Glu in position 10 were more active than the homolog with Asp at this position. This trend was also found with the corresponding linear pheromones, suggesting that a gamma-carbonyl in position 10 is an important determinant of pheromone potency. The cyclic peptides had from 50- to 20000-fold lower affinities for the alpha-factor receptor than for [Nle12]-alpha-factor, as judged using a competition binding assay. Circular dichroism studies indicate that the cyclic lactam-containing region of cyclo7.10[Orn7, Glu10,Nle12]-alpha-factor retains a beta-turn-like structure similar to that found in the corresponding model tetrapeptide. The results show that covalently constrained analogs of the linear pheromone can maintain biological activity, despite binding poorly to the receptor, and indicate that a beta-turn-like structure in the center of the pheromone allows signal transduction"
Keywords:"Binding, Competitive Circular Dichroism Fungal Proteins/chemistry Lactams Mating Factor Peptides/*chemistry Peptides, Cyclic/chemistry Pheromones/*chemistry Protein Structure, Secondary Saccharomyces cerevisiae/*chemistry/growth & development Structure-Ac;"
Notes:"MedlineYang, W McKinney, A Becker, J M Naider, F eng GM22086/GM/NIGMS NIH HHS/ GM22087/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1995/01/31 Biochemistry. 1995 Jan 31; 34(4):1308-15. doi: 10.1021/bi00004a025"

 
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