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« Previous AbstractEnhanced oral availability/pheromonotropic activity of peptidase-resistant topical amphiphilic analogs of pyrokinin/PBAN insect neuropeptides    Next AbstractBiostable beta-amino acid PK/PBAN analogs: agonist and antagonist properties »

Peptides


Title:"An amphiphilic, PK/PBAN analog is a selective pheromonotropic antagonist that penetrates the cuticle of a heliothine insect"
Author(s):Nachman RJ; Teal PE; Aziz OB; Davidovitch M; Zubrzak P; Altstein M;
Address:"Areawide Pest Management Research, Southern Plains Agricultural Research Center, U.S. Department of Agriculture, College Station, TX 77845, USA. nachman@tamu.edu"
Journal Title:Peptides
Year:2009
Volume:20081017
Issue:3
Page Number:616 - 621
DOI: 10.1016/j.peptides.2008.09.024
ISSN/ISBN:0196-9781 (Print) 0196-9781 (Linking)
Abstract:"A linear pyrokinin (PK)/pheromone biosynthesis activating neuropeptide (PBAN) antagonist lead (RYF[dF]PRLa) was structurally modified to impart amphiphilic properties to enhance its ability to transmigrate the hydrophobic cuticle of noctuid moth species and yet retain aqueous solubility in the hemolymph to reach target PK/PBAN receptors within the internal insect environment. The resulting novel PK/PBAN analog, Hex-Suc-A[dF]PRLa (PPK-AA), was synthesized and evaluated as an antagonist in a pheromonotropic assay in Heliothis peltigera against 4 natural PK/PBAN peptide elicitors (PBAN; pheromonotropin, PT; myotropin, MT; leucopyrokinin, LPK) and in a melanotropic assay in Spodoptera littoralis against 3 natural PK/PBAN peptide elicitors (PBAN, PT, LPK). The analog proved to be a potent and efficacious inhibitor of sex pheromone biosynthesis elicited by PBAN (84% at 100 pmol) and PT (54% at 100 pmol), but not by MT and LPK. PPK-AA is a selective pure antagonist (i.e., does not exhibit any agonistic activity) as it failed to inhibit melanization elicited by any of the natural PK/PBAN peptides. The analog was shown to transmigrate isolated cuticle dissected from adult female Heliothis virescens moths to a high extent of 25-30% (130-150 pmol), representing physiologically significant quantities. PPK-AA represents a significant addition to the arsenal of tools available to arthropod endocrinologists studying the endogenous mechanisms of PK/PBAN regulated processes, and a prototype for the development of environmentally friendly pest management agents capable of disrupting the critical process of reproduction"
Keywords:Animals Biological Assay Female Melanotrophs/drug effects Moths/*drug effects Neuropeptides/chemical synthesis/*pharmacology Oligopeptides Pyrrolidonecarboxylic Acid/analogs & derivatives Sex Attractants/*antagonists & inhibitors/biosynthesis Surface-Acti;
Notes:"MedlineNachman, Ronald J Teal, Peter E A Aziz, Orna Ben Davidovitch, Michael Zubrzak, Pawel Altstein, Miriam eng Research Support, Non-U.S. Gov't 2008/11/11 Peptides. 2009 Mar; 30(3):616-21. doi: 10.1016/j.peptides.2008.09.024. Epub 2008 Oct 17"

 
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