Evidence map›Paper›PMID 20513760›Full record

ArticleThe Journal of general physiology2010

Adaptive behavior of bacterial mechanosensitive channels is coupled to membrane mechanics.

Vladislav Belyy, Kishore Kamaraju, Bradley Akitake, Andriy Anishkin, Sergei Sukharev

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 75 citations in OpenAlex.

  1. The MscS channel frombioRxiv : the preprint server for biology · 2026
    Article
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  3. Article
  4. Review
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  6. Article
  7. Article
  8. Review
  9. Physics of mechanotransduction by Piezo ion channels.The Journal of general physiology · 2022
    Review
  10. Article
  11. Article
  12. Cellular transduction of mechanical oscillations in plants by the plasma-membrane mechanosensitive channel MSL10.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Article
  15. Article
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  20. Dynamics of Escherichia coli's passive response to a sudden decrease in external osmolarity.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Vladislav BelyyDepartment of Biology, University of Maryland, College Park, MD 20742, USA.
Kishore Kamaraju
Bradley Akitake
Andriy Anishkin
Sergei Sukharev
University of Maryland, College Park · US

Funding

Functional Cycle of a Mechanosensitive ChannelR01GM075225 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI SUKHAREV, SERGEI I · 2006 to 2009
$1.1M
Howard Hughes Medical InstituteNIGMS NIH HHS GM075225NIGMS NIH HHS R01 GM075225NINDS NIH HHS NS03931405A
6 · The paper itself

Abstract

Mechanosensitive channel of small conductance (MscS), a tension-driven osmolyte release valve residing in the inner membrane of Escherichia coli, exhibits a complex adaptive behavior, whereas its functional counterpart, mechanosensitive channel of large conductance (MscL), was generally considered nonadaptive. In this study, we show that both channels exhibit similar adaptation in excised patches, a process that is completely separable from inactivation prominent only in MscS. When a membrane patch is held under constant pressure, adaptation of both channels is manifested as a reversible current decline. Their dose-response curves recorded with 1-10-s ramps of pressure are shifted toward higher tension relative to the curves measured with series of pulses, indicating decreased tension sensitivity. Prolonged exposure of excised patches to subthreshold tensions further shifts activation curves for both MscS and MscL toward higher tension with similar magnitude and time course. Whole spheroplast MscS recordings performed with simultaneous imaging reveal activation curves with a midpoint tension of 7.8 mN/m and the slope corresponding to approximately 15-nm(2) in-plane expansion. Inactivation was retained in whole spheroplast mode, but no adaptation was observed. Similarly, whole spheroplast recordings of MscL (V23T mutant) indicated no adaptation, which was present in excised patches. MscS activities tried in spheroplast-attached mode showed no adaptation when the spheroplasts were intact, but permeabilized spheroplasts showed delayed adaptation, suggesting that the presence of membrane breaks or edges causes adaptation. We interpret this in the framework of the mechanics of the bilayer couple linking adaptation of channels in excised patches to the relaxation of the inner leaflet that is not in contact with the glass pipette. Relaxation of one leaflet results in asymmetric redistribution of tension in the bilayer that is less favorable for channel opening.

Indexed as

Ion Channel GatingMechanotransduction, CellularAdaptation, PhysiologicalEscherichia coliEscherichia coli ProteinsIon ChannelsMembrane PotentialsModels, MolecularPatch-Clamp TechniquesPressureProtein ConformationSpheroplastsStructure-Activity RelationshipTime FactorsEscherichia coli ProteinsIon ChannelsMscL protein, E coliMscS protein, E coli

Identifiers

PMID20513760
PMCPMC2888061
OpenAlexW1999164955

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.