High-throughput random mutagenesis screen reveals TRPM8 residues specifically required for activation by menthol View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-03-05

AUTHORS

Michael Bandell, Adrienne E Dubin, Matt J Petrus, Anthony Orth, Jayanti Mathur, Sun Wook Hwang, Ardem Patapoutian

ABSTRACT

Menthol is a cooling compound derived from mint leaves and is extensively used as a flavoring chemical. Menthol activates transient receptor potential melastatin 8 (TRPM8), an ion channel also activated by cold, voltage and phosphatidylinositol-4,5-bisphosphate (PIP2). Here we investigated the mechanism by which menthol activates mouse TRPM8. Using a new high-throughput approach, we screened a random mutant library consisting of ∼14,000 individual TRPM8 mutants for clones that are affected in their response to menthol while retaining channel function. We identified determinants of menthol sensitivity in two regions: putative transmembrane segment 2 (S2) and the C-terminal TRP domain. Analysis of these mutants indicated that activation by menthol involves a gating mechanism distinct and separable from gating by cold, voltage or PIP2. Notably, TRP domain mutations mainly attenuated menthol efficacy, suggesting that this domain influences events downstream of initial binding. In contrast, S2 mutations strongly shifted the concentration dependence of menthol activation, raising the possibility that S2 influences menthol binding.Note: The AOP version of this article was corrected on 19 March 2006. Please see the PDF for details. More... »

PAGES

493-500

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nn1665

DOI

http://dx.doi.org/10.1038/nn1665

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1021696391

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16520735


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