Evidence map›Paper›PMID 22108384›Full record

ArticlemBio2011

Unbalanced charge distribution as a determinant for dependence of a subset of Escherichia coli membrane proteins on the membrane insertase YidC.

Andrew N Gray, Josephine M Henderson-Frost, Dana Boyd, Shirin Sharafi, Shirin Shirafi, Hironori Niki, Marcia B Goldberg

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in mBio, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. The versatile role of YidC in membrane protein biosynthesis and quality control.Biochimica et biophysica acta. Molecular cell research · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. YidC/Alb3/Oxa1 Family of Insertases.The Journal of biological chemistry · 2015
    Review
  9. Article
  10. Article
  11. Article
  12. Enhanced group II intron retrohoming in magnesium-deficient Escherichia coli via selection of mutations in the ribozyme core.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  13. Article
  14. The Sec-dependent pathway.Research in microbiology
    Review
4 · The record

Corrections and comments

  • Erratum issued
    Shirafi, Shirin [corrected to Sharafi, Shirin]
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Andrew N GrayDepartment of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Josephine M Henderson-Frost
Dana Boyd
Shirin Sharafi
Shirin Shirafi
Hironori Niki
Marcia B Goldberg
Massachusetts General Hospital · USHarvard University · USNational Institute of Genetics · JP

Funding

MECHANISM AND FUNCTION OF UNIPOLARITY OF SHIGELLA ICSAR01AI035817 · NIAID · YESHIVA UNIVERSITY · PI GOLDBERG, MARCIA B · 1994 to 2009
$3.9M
NIAID NIH HHS AI035817NIAID NIH HHS R01 AI035817
6 · The paper itself

Abstract

unlabelledMembrane proteins are involved in numerous essential cell processes, including transport, gene regulation, motility, and metabolism. To function properly, they must be inserted into the membrane and folded correctly. YidC, an essential protein in Escherichia coli with homologues in other bacteria, Archaea, mitochondria, and chloroplasts, functions by incompletely understood mechanisms in the insertion and folding of certain membrane proteins. Using a genome-scale approach, we identified 69 E. coli membrane proteins that, in the absence of YidC, exhibited aberrant localization by microscopy. Further examination of a subset revealed biochemical defects in membrane insertion in the absence of YidC, indicating their dependence on YidC for proper membrane insertion or folding. Membrane proteins possessing an unfavorable distribution of positively charged residues were significantly more likely to depend on YidC for membrane insertion. Correcting the charge distribution of a charge-unbalanced YidC-dependent membrane protein abrogated its requirement for YidC, while perturbing the charge distribution of a charge-balanced YidC-independent membrane protein rendered it YidC dependent, demonstrating that charge distribution can be a necessary and sufficient determinant of YidC dependence. These findings provide insights into a mechanism by which YidC promotes proper membrane protein biogenesis and suggest a critical function of YidC in all organisms and organelles that express it. IMPORTANCE: Biological membranes are fundamental components of cells, providing barriers that enclose the cell and separate compartments. Proteins inserted into biological membranes serve critical functions in molecular transport, molecular partitioning, and other essential cell processes. The mechanisms involved in the insertion of proteins into membranes, however, are incompletely understood. The YidC protein is critical for the insertion of a subset of proteins into membranes across an evolutionarily wide group of organisms. Here we identify a large group of proteins that depend on YidC for membrane insertion in Escherichia coli, and we identify unfavorable distribution of charge as an important determinant of YidC dependence for proper membrane insertion.

Indexed as

Cell MembraneEscherichia coliEscherichia coli ProteinsMembrane ProteinsMembrane Transport ProteinsProtein TransportEscherichia coli ProteinsMembrane ProteinsMembrane Transport ProteinsYIDC protein, E coli

Identifiers

PMID22108384
PMCPMC3225971
OpenAlexW2106424758

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.