Evidence map›Paper›PMID 31941768›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2020

Life with Bacterial Mechanosensitive Channels, from Discovery to Physiology to Pharmacological Target.

Paul Blount, Irene Iscla

Abstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Lipid Regulation of Mechanosensitive Ion Channels.International journal of molecular sciences · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Effects ofMicroorganisms · 2024
    Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Mechanosensitive channel MscL gating transitions coupling with constriction point shift.Protein science : a publication of the Protein Society · 2024
    Article
  18. Article
  19. Article
  20. Mechanosensing in Metabolism.Comprehensive Physiology · 2023
    Review
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

2 authors.

Paul BlountDepartment of Physiology, UT Southwestern Medical Center, Dallas, Texas, USA paul.blount@utsouthwestern.edu irene.iscla@utsouthwestern.edu.
Irene IsclaDepartment of Physiology, UT Southwestern Medical Center, Dallas, Texas, USA paul.blount@utsouthwestern.edu irene.iscla@utsouthwestern.edu.

Funding

Using Small Compounds as Probes for Studying Mechanosensitive Channel GatingR01GM121780 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI BLOUNT, PAUL · 2017 to 2020
$1.1M
NIGMS NIH HHS R01 GM121780
6 · The paper itself

Abstract

General principles in biology have often been elucidated from the study of bacteria. This is true for the bacterial mechanosensitive channel of large conductance, MscL, the channel highlighted in this review. This channel functions as a last-ditch emergency release valve discharging cytoplasmic solutes upon decreases in osmotic environment. Opening the largest gated pore, MscL passes molecules up to 30 Å in diameter; exaggerated conformational changes yield advantages for study, including

Indexed as

Anti-Bacterial AgentsBacteriaBacterial Physiological PhenomenaCell MembraneEscherichia coliEscherichia coli ProteinsIon ChannelsOsmoregulationAnti-Bacterial AgentsEscherichia coli ProteinsIon ChannelsMscL protein, E colidrug targetsion channelsmechanosensitive channelsmembrane biophysicsmembrane channel proteinsmembrane transportosmoregulationphysiology

Identifiers

PMID31941768
PMCPMC7167205

What OpenQuestion holds

Textmetadata
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.