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The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis

Although mechanoelectrical transducer (MET) channels have been extensively studied, uncertainty persists about their molecular architecture and single-channel conductance. We made electrical measurements from mouse cochlear outer hair cells (OHCs) to reexamine the MET channel conductance comparing t...

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Detalles Bibliográficos
Autores principales: Beurg, Maryline, Nam, Jong-Hoon, Fettiplace, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383808/
https://www.ncbi.nlm.nih.gov/pubmed/34411238
http://dx.doi.org/10.1085/jgp.202112959
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author Beurg, Maryline
Nam, Jong-Hoon
Fettiplace, Robert
author_facet Beurg, Maryline
Nam, Jong-Hoon
Fettiplace, Robert
author_sort Beurg, Maryline
collection PubMed
description Although mechanoelectrical transducer (MET) channels have been extensively studied, uncertainty persists about their molecular architecture and single-channel conductance. We made electrical measurements from mouse cochlear outer hair cells (OHCs) to reexamine the MET channel conductance comparing two different methods. Analysis of fluctuations in the macroscopic currents showed that the channel conductance in apical OHCs determined from nonstationary noise analysis was about half that of single-channel events recorded after tip link destruction. We hypothesized that this difference reflects a bandwidth limitation in the noise analysis, which we tested by simulations of stochastic fluctuations in modeled channels. Modeling indicated that the unitary conductance depended on the relative values of the channel activation time constant and the applied low-pass filter frequency. The modeling enabled the activation time constant of the channel to be estimated for the first time, yielding a value of only a few microseconds. We found that the channel conductance, assayed with both noise and recording of single-channel events, was reduced by a third in a new deafness mutant, Tmc1 p.D528N. Our results indicate that noise analysis is likely to underestimate MET channel amplitude, which is better characterized from recordings of single-channel events.
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spelling pubmed-83838082021-09-01 The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis Beurg, Maryline Nam, Jong-Hoon Fettiplace, Robert J Gen Physiol Article Although mechanoelectrical transducer (MET) channels have been extensively studied, uncertainty persists about their molecular architecture and single-channel conductance. We made electrical measurements from mouse cochlear outer hair cells (OHCs) to reexamine the MET channel conductance comparing two different methods. Analysis of fluctuations in the macroscopic currents showed that the channel conductance in apical OHCs determined from nonstationary noise analysis was about half that of single-channel events recorded after tip link destruction. We hypothesized that this difference reflects a bandwidth limitation in the noise analysis, which we tested by simulations of stochastic fluctuations in modeled channels. Modeling indicated that the unitary conductance depended on the relative values of the channel activation time constant and the applied low-pass filter frequency. The modeling enabled the activation time constant of the channel to be estimated for the first time, yielding a value of only a few microseconds. We found that the channel conductance, assayed with both noise and recording of single-channel events, was reduced by a third in a new deafness mutant, Tmc1 p.D528N. Our results indicate that noise analysis is likely to underestimate MET channel amplitude, which is better characterized from recordings of single-channel events. Rockefeller University Press 2021-08-19 /pmc/articles/PMC8383808/ /pubmed/34411238 http://dx.doi.org/10.1085/jgp.202112959 Text en © 2021 Beurg et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Beurg, Maryline
Nam, Jong-Hoon
Fettiplace, Robert
The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title_full The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title_fullStr The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title_full_unstemmed The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title_short The speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
title_sort speed of the hair cell mechanotransducer channel revealed by fluctuation analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383808/
https://www.ncbi.nlm.nih.gov/pubmed/34411238
http://dx.doi.org/10.1085/jgp.202112959
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