Evidence map›Paper›PMID 23416054›Full record

ArticleCell reports2013

Chimeras reveal a single lipid-interface residue that controls MscL channel kinetics as well as mechanosensitivity.

Li-Min Yang, Dalian Zhong, Paul Blount

Abstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Asymmetric Nature of MscL Opening Revealed by Molecular Dynamics Simulations.Journal of chemical information and modeling · 2025
    Article
  3. Article
  4. Mechanosensitive channel MscL gating transitions coupling with constriction point shift.Protein science : a publication of the Protein Society · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. A new antibiotic with potent activity targets MscL.The Journal of antibiotics · 2015
    Article
  14. Article
  15. Electrostatics at the membrane define MscL channel mechanosensitivity and kinetics.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
  16. Article
  17. 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

3 authors.

Li-Min YangDepartment of Physiology, UT Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9040, USA.
Dalian Zhong
Paul Blount

Funding

MOLECULAR MECHANISMS OF MECHANOSENSITIVE CHANNEL GATINGR01GM061028 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI BLOUNT, PAUL · 2000 to 2017
$4.7M
High Throughput Screening: Bacterial Mechanosensitive Channels as Drug TargetsR03AI080807 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI BLOUNT, PAUL · 2009 to 2010
$157k
NIAID NIH HHS AI080807NIAID NIH HHS R03 AI080807NIGMS NIH HHS GM061028NIGMS NIH HHS R01 GM061028
6 · The paper itself

Abstract

MscL, the highly conserved bacterial mechanosensitive channel of large conductance, serves as an osmotic "emergency release valve," is among the best-studied mechanosensors, and is a paradigm of how a channel senses and responds to membrane tension. Although all homologs tested thus far encode channel activity, many show functional differences. We tested Escherichia coli and Staphylococcus aureus chimeras and found that the periplasmic region of the protein, particularly E. coli I49 and the equivalent S. aureus F47 at the periplasmic lipid-aqueous interface of the first transmembrane domain, drastically influences both the open dwell time and the threshold of channel opening. One mutant shows a severe hysteresis, confirming the importance of this residue in determining the energy barriers for channel gating. We propose that this site acts similarly to a spring for a clasp knife, adjusting the resistance for obtaining and stabilizing an open or closed channel structure.

Indexed as

Amino Acid SequenceDNA Mutational AnalysisEscherichia coliEscherichia coli ProteinsHydrophobic and Hydrophilic InteractionsIon Channel GatingIon ChannelsKineticsMolecular Sequence DataMutagenesis, Site-DirectedPeriplasmProtein Structure, TertiaryRecombinant Fusion ProteinsSequence AlignmentStaphylococcus aureusEscherichia coli ProteinsIon ChannelsMscL protein, E coliRecombinant Fusion Proteins

Identifiers

PMID23416054
PMCPMC3593973

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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.