Evidence map›Paper›PMID 19931583›Full record

ArticlePeptides2010

Antimicrobial mechanism of pore-forming protegrin peptides: 100 pores to kill E. coli.

Dan Bolintineanu, Ehsan Hazrati, H Ted Davis, Robert I Lehrer, Yiannis N Kaznessis

Abstract read
In one paragraph

Article in Peptides, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Insect Antimicrobial Peptides as Guardians of Immunity and Beyond: A Review.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Concerted Rolling and Penetration of Peptides during Membrane Binding.Journal of chemical theory and computation · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Computational studies of peptide-induced membrane pore formation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  14. Manganese transport is essential for NEnvironmental microbiology · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Antimicrobial combinations: Bliss independence and Loewe additivity derived from mechanistic multi-hit models.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Article
  19. Review
  20. 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 2 institutions in 1 country.

Dan BolintineanuDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN 55455-0132, USA.
Ehsan Hazrati
H Ted Davis
Robert I Lehrer
Yiannis N Kaznessis
University of Minnesota · USUniversity of California, Los Angeles · US

Funding

Computational Modeling /Design of Antimicrobial PeptidesR01GM070989 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI KAZNESSIS, YIANNIS · 2005 to 2009
$1.1M
NIGMS NIH HHS GM 070989NIGMS NIH HHS R01 GM070989
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs), important effector molecules of the innate immune system, also provide templates for designing novel antibiotics. Protegrin, an especially potent AMP found in porcine leukocytes, was recently shown to form octameric transmembrane pores. We have employed a combination of experiments and models spanning length scales from the atomistic to the cellular level in order to elucidate the microbicidal mechanism of protegrin. Comparison of the modeling and experimental data suggests that approximately 10-100 protegrin pores are necessary to explain the observed rates of potassium leakage and Escherichia coli death in exponential-phase bacteria. The kinetics of viability loss suggest that bacterial death results largely from uncontrolled ion exchange processes and decay of transmembrane potential. However, ion exchange processes alone cannot account for the experimentally observed cell swelling and osmotic lysis-a redundant "overkill" mechanism most likely to occur in locales with high protegrin concentrations. Although our study is limited to protegrin and E. coli, the timeline of events described herein is likely shared by other AMPs that act primarily by permeabilizing microbial membranes. This work provides many of the missing links in describing antimicrobial action, as well as providing a quantitative connection between several previous experimental and simulation studies of protegrin.

Indexed as

Models, TheoreticalAnti-Infective AgentsAntimicrobial Cationic PeptidesEscherichia coliIonsMembrane PotentialsMolecular Dynamics SimulationProtein ConformationAnti-Infective AgentsAntimicrobial Cationic PeptidesIons

Identifiers

PMID19931583
PMCPMC2825693
OpenAlexW2097096403

What OpenQuestion holds

Textmetadata
LicenceTDM
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.