Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel

TRPV are cation channels activated by physical and chemical stimuli. Here the authors show that nicotinamide is a soluble, endogenous agonist for orthologous TRPV channels fromC. elegans and Drosophila, unveiling a metabolic-based regulation for TRPV channel activity.

Bibliographic Details
Main Authors: Awani Upadhyay, Aditya Pisupati, Timothy Jegla, Matt Crook, Keith J. Mickolajczyk, Matthew Shorey, Laura E. Rohan, Katherine A. Billings, Melissa M. Rolls, William O. Hancock, Wendy Hanna-Rose
Format: Article
Language:English
Published: Nature Portfolio 2016-10-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms13135
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author Awani Upadhyay
Aditya Pisupati
Timothy Jegla
Matt Crook
Keith J. Mickolajczyk
Matthew Shorey
Laura E. Rohan
Katherine A. Billings
Melissa M. Rolls
William O. Hancock
Wendy Hanna-Rose
author_facet Awani Upadhyay
Aditya Pisupati
Timothy Jegla
Matt Crook
Keith J. Mickolajczyk
Matthew Shorey
Laura E. Rohan
Katherine A. Billings
Melissa M. Rolls
William O. Hancock
Wendy Hanna-Rose
author_sort Awani Upadhyay
collection DOAJ
description TRPV are cation channels activated by physical and chemical stimuli. Here the authors show that nicotinamide is a soluble, endogenous agonist for orthologous TRPV channels fromC. elegans and Drosophila, unveiling a metabolic-based regulation for TRPV channel activity.
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spelling doaj.art-dfd0ef3108b94258be603a05f7ad9bb72022-12-21T19:25:59ZengNature PortfolioNature Communications2041-17232016-10-017111110.1038/ncomms13135Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channelAwani Upadhyay0Aditya Pisupati1Timothy Jegla2Matt Crook3Keith J. Mickolajczyk4Matthew Shorey5Laura E. Rohan6Katherine A. Billings7Melissa M. Rolls8William O. Hancock9Wendy Hanna-Rose10Department of Biochemistry and Molecular Biology, The Pennsylvania State UniversityDepartment of Biology, The Pennsylvania State UniversityDepartment of Biology, The Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology, The Pennsylvania State UniversityDepartment of Biomedical Engineering, The Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology, The Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology, The Pennsylvania State UniversityDepartment of Biology, The Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology, The Pennsylvania State UniversityDepartment of Biomedical Engineering, The Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology, The Pennsylvania State UniversityTRPV are cation channels activated by physical and chemical stimuli. Here the authors show that nicotinamide is a soluble, endogenous agonist for orthologous TRPV channels fromC. elegans and Drosophila, unveiling a metabolic-based regulation for TRPV channel activity.https://doi.org/10.1038/ncomms13135
spellingShingle Awani Upadhyay
Aditya Pisupati
Timothy Jegla
Matt Crook
Keith J. Mickolajczyk
Matthew Shorey
Laura E. Rohan
Katherine A. Billings
Melissa M. Rolls
William O. Hancock
Wendy Hanna-Rose
Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
Nature Communications
title Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
title_full Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
title_fullStr Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
title_full_unstemmed Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
title_short Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel
title_sort nicotinamide is an endogenous agonist for a c elegans trpv osm 9 and ocr 4 channel
url https://doi.org/10.1038/ncomms13135
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