Allosteric antagonism of insect odorant receptor ion channels

At a molecular level, insects utilize members of several highly divergent and unrelated families of cell-surface chemosensory receptors for detection of volatile odorants. Most odors are detected via a family of odorant receptors (ORs), which form heteromeric complexes consisting of a well-conserved...

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Veröffentlicht in:PloS one 2012-01, Vol.7 (1), p.e30304
Hauptverfasser: Jones, Patrick L, Pask, Gregory M, Romaine, Ian M, Taylor, Robert W, Reid, Paul R, Waterson, Alex G, Sulikowski, Gary A, Zwiebel, Laurence J
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container_title PloS one
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Pask, Gregory M
Romaine, Ian M
Taylor, Robert W
Reid, Paul R
Waterson, Alex G
Sulikowski, Gary A
Zwiebel, Laurence J
description At a molecular level, insects utilize members of several highly divergent and unrelated families of cell-surface chemosensory receptors for detection of volatile odorants. Most odors are detected via a family of odorant receptors (ORs), which form heteromeric complexes consisting of a well-conserved OR co-receptor (Orco) ion channel and a non-conserved tuning OR that provides coding specificity to each complex. Orco functions as a non-selective cation channel and is expressed in the majority of olfactory receptor neurons (ORNs). As the destructive behaviors of many insects are principally driven by olfaction, Orco represents a novel target for behavior-based control strategies. While many natural and synthetic odorants have been shown to agonize Orco/Or complexes, only a single direct Orco modulator, VUAA1, has been described. In an effort to identify additional Orco modulators, we have investigated the structure/activity relationships around VUAA1. A search of our compound library identified several VUAA1 analogs that were selected for evaluation against HEK cells expressing Orco from the malaria vector Anopheles gambiae (AgOrco). While the majority of compounds displayed no activity, many of these analogs possess no intrinsic efficacy, but instead, act as competitive VUAA1 antagonists. Using calcium mobilization assays, patch clamp electrophysiology, and single sensillum in vivo recording, we demonstrate that one such candidate, VU0183254, is a specific allosteric modulator of OR signaling, capable of broadly inhibiting odor-mediated OR complex activation. We have described and characterized the first Orco antagonist, that is capable of non-competitively inhibiting odorant-evoked activation of OR complexes, thereby providing additional insight into the structure/function of this unique family of ligand-gated ion channels. While Orco antagonists are likely to have limited utility in insect control programs, they represent important pharmacological tools that will facilitate the investigation of the molecular mechanisms underlying insect olfactory signal transduction.
doi_str_mv 10.1371/journal.pone.0030304
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This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Most odors are detected via a family of odorant receptors (ORs), which form heteromeric complexes consisting of a well-conserved OR co-receptor (Orco) ion channel and a non-conserved tuning OR that provides coding specificity to each complex. Orco functions as a non-selective cation channel and is expressed in the majority of olfactory receptor neurons (ORNs). As the destructive behaviors of many insects are principally driven by olfaction, Orco represents a novel target for behavior-based control strategies. While many natural and synthetic odorants have been shown to agonize Orco/Or complexes, only a single direct Orco modulator, VUAA1, has been described. In an effort to identify additional Orco modulators, we have investigated the structure/activity relationships around VUAA1. A search of our compound library identified several VUAA1 analogs that were selected for evaluation against HEK cells expressing Orco from the malaria vector Anopheles gambiae (AgOrco). 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inhibitors</subject><subject>Insect Proteins - genetics</subject><subject>Insect Proteins - physiology</subject><subject>Insects</subject><subject>Ion channels</subject><subject>Ion channels (ligand-gated)</subject><subject>Ion Channels - agonists</subject><subject>Ion Channels - antagonists &amp; inhibitors</subject><subject>Ion Channels - genetics</subject><subject>Ion Channels - physiology</subject><subject>Malaria</subject><subject>Medicine</subject><subject>Modulators</subject><subject>Molecular modelling</subject><subject>Molecular Structure</subject><subject>Mosquitoes</subject><subject>Neuromodulation</subject><subject>Odorant receptors</subject><subject>Odorants</subject><subject>Odors</subject><subject>Olfaction</subject><subject>Olfactory receptor neurons</subject><subject>Olfactory Receptor Neurons - drug effects</subject><subject>Olfactory Receptor Neurons - physiology</subject><subject>Organic Chemicals - chemistry</subject><subject>Organic Chemicals - pharmacology</subject><subject>Pharmacology</subject><subject>Phenothiazines - chemistry</subject><subject>Phenothiazines - pharmacology</subject><subject>Receptors</subject><subject>Receptors, Odorant - agonists</subject><subject>Receptors, Odorant - antagonists &amp; 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, Patrick L</au><au>Pask, Gregory M</au><au>Romaine, Ian M</au><au>Taylor, Robert W</au><au>Reid, Paul R</au><au>Waterson, Alex G</au><au>Sulikowski, Gary A</au><au>Zwiebel, Laurence J</au><au>Nighorn, Alan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allosteric antagonism of insect odorant receptor ion channels</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-01-17</date><risdate>2012</risdate><volume>7</volume><issue>1</issue><spage>e30304</spage><pages>e30304-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>At a molecular level, insects utilize members of several highly divergent and unrelated families of cell-surface chemosensory receptors for detection of volatile odorants. Most odors are detected via a family of odorant receptors (ORs), which form heteromeric complexes consisting of a well-conserved OR co-receptor (Orco) ion channel and a non-conserved tuning OR that provides coding specificity to each complex. Orco functions as a non-selective cation channel and is expressed in the majority of olfactory receptor neurons (ORNs). As the destructive behaviors of many insects are principally driven by olfaction, Orco represents a novel target for behavior-based control strategies. While many natural and synthetic odorants have been shown to agonize Orco/Or complexes, only a single direct Orco modulator, VUAA1, has been described. In an effort to identify additional Orco modulators, we have investigated the structure/activity relationships around VUAA1. A search of our compound library identified several VUAA1 analogs that were selected for evaluation against HEK cells expressing Orco from the malaria vector Anopheles gambiae (AgOrco). While the majority of compounds displayed no activity, many of these analogs possess no intrinsic efficacy, but instead, act as competitive VUAA1 antagonists. Using calcium mobilization assays, patch clamp electrophysiology, and single sensillum in vivo recording, we demonstrate that one such candidate, VU0183254, is a specific allosteric modulator of OR signaling, capable of broadly inhibiting odor-mediated OR complex activation. We have described and characterized the first Orco antagonist, that is capable of non-competitively inhibiting odorant-evoked activation of OR complexes, thereby providing additional insight into the structure/function of this unique family of ligand-gated ion channels. While Orco antagonists are likely to have limited utility in insect control programs, they represent important pharmacological tools that will facilitate the investigation of the molecular mechanisms underlying insect olfactory signal transduction.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22272331</pmid><doi>10.1371/journal.pone.0030304</doi><tpages>e30304</tpages><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Activation
Allosteric properties
Allosteric Regulation - drug effects
Analogs
Animal behavior
Animals
Anopheles
Anopheles gambiae
Antagonists
Biology
Calcium
Calcium antagonists
Cell surface
Cellular signal transduction
Chemistry
Chemoreception
Coding
Control programs
Culicidae
Dose-Response Relationship, Drug
Drosophila
Electrophysiology
Evoked Potentials - drug effects
Female
HEK293 Cells
Humans
Insect control
Insect Proteins - agonists
Insect Proteins - antagonists & inhibitors
Insect Proteins - genetics
Insect Proteins - physiology
Insects
Ion channels
Ion channels (ligand-gated)
Ion Channels - agonists
Ion Channels - antagonists & inhibitors
Ion Channels - genetics
Ion Channels - physiology
Malaria
Medicine
Modulators
Molecular modelling
Molecular Structure
Mosquitoes
Neuromodulation
Odorant receptors
Odorants
Odors
Olfaction
Olfactory receptor neurons
Olfactory Receptor Neurons - drug effects
Olfactory Receptor Neurons - physiology
Organic Chemicals - chemistry
Organic Chemicals - pharmacology
Pharmacology
Phenothiazines - chemistry
Phenothiazines - pharmacology
Receptors
Receptors, Odorant - agonists
Receptors, Odorant - antagonists & inhibitors
Receptors, Odorant - genetics
Receptors, Odorant - physiology
Signal transduction
Signaling
Software
Structure-Activity Relationship
Structure-function relationships
Studies
Thioglycolates - chemistry
Thioglycolates - pharmacology
Triazoles - chemistry
Triazoles - pharmacology
Vector-borne diseases
title Allosteric antagonism of insect odorant receptor ion channels
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