Evidence map›Paper›PMID 21166473›Full record

ArticleBiochemistry2011

A thermodynamic approach to the mechanism of cell-penetrating peptides in model membranes.

Alesia N McKeown, Jeffrey L Naro, Laura J Huskins, Paulo F Almeida

Abstract read
In one paragraph

Article in Biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Latarcins: versatile spider venom peptides.Cellular and molecular life sciences : CMLS · 2015
    Review
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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

4 authors at 1 institution in 1 country.

Alesia N McKeownDepartment of Chemistry and Biochemistry, University of North Carolina, Wilmington, North Carolina 28403, United States.
Jeffrey L Naro
Laura J Huskins
Paulo F Almeida
University of North Carolina Wilmington · US

Funding

Mechanisms of amphipathic and cargo delivery peptidesR15GM072507 · NIGMS · UNIVERSITY OF NORTH CAROLINA WILMINGTON · PI ALMEIDA, PAULO F · 2005 to 2012
$758k
NIGMS NIH HHS GM072507NIGMS NIH HHS R15 GM072507
6 · The paper itself

Abstract

We report a first test of the hypothesis that the mechanism of antimicrobial, cytolytic, and amphipathic cell-penetrating peptides in model membranes is determined by the thermodynamics of insertion of the peptide into the lipid bilayer from the surface-associated state. Three peptides were designed with minimal mutations relative to the sequence of TP10W, the Y3W variant of transportan 10, which is a helical, amphipathic cell-penetrating peptide previously studied. Binding to 1-palmitoyl-2-oleoylphosphatidylcholine (POPC) membranes and release of dye from those vesicles were assessed by stopped-flow fluorescence, and the secondary structure of the peptides on the membrane was determined by circular dichroism. The Gibbs energy of binding determined experimentally was in excellent agreement with that calculated using the Wimley-White interfacial hydrophobicity scale, taking into account the helical content of the membrane-associated peptide. Release of dye from POPC vesicles remained graded, as predicted by the hypothesis. More significantly, as the Gibbs energy of insertion into the bilayer became more unfavorable, which was estimated using the Wimley-White octanol hydrophobicity scale, dye release became slower, in quantitative agreement with the prediction.

Indexed as

Amino Acid SequenceCell MembraneCell-Penetrating PeptidesKineticsLipid BilayersModels, BiologicalMolecular Sequence DataThermodynamicsCell-Penetrating PeptidesLipid Bilayers

Identifiers

PMID21166473
PMCPMC3035854
OpenAlexW2043153340

What OpenQuestion holds

Textmetadata
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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.