Evidence map›Paper›PMID 27874004›Full record

ArticleNature communications2016

Spontaneous formation of structurally diverse membrane channel architectures from a single antimicrobial peptide.

Yukun Wang, Charles H Chen, Dan Hu, Martin B Ulmschneider, Jakob P Ulmschneider

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

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  20. Predicting Membrane-Active Peptide Dynamics in Fluidic Lipid Membranes.Methods in molecular biology (Clifton, N.J.) · 2022
    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.

Yukun WangInstitute of Natural Sciences, Shanghai Jiao-Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Charles H ChenInstitute of NanoBioTechnology, Johns Hopkins University, 204C Schaffer Hall, 3400 North Charles Street, Baltimore, Maryland 21218-2681, USA.
Dan HuInstitute of Natural Sciences, Shanghai Jiao-Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Martin B UlmschneiderInstitute of NanoBioTechnology, Johns Hopkins University, 204C Schaffer Hall, 3400 North Charles Street, Baltimore, Maryland 21218-2681, USA.
Jakob P UlmschneiderInstitute of Natural Sciences, Shanghai Jiao-Tong University, 800 Dongchuan Road, Shanghai 200240, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many antimicrobial peptides (AMPs) selectively target and form pores in microbial membranes. However, the mechanisms of membrane targeting, pore formation and function remain elusive. Here we report an experimentally guided unbiased simulation methodology that yields the mechanism of spontaneous pore assembly for the AMP maculatin at atomic resolution. Rather than a single pore, maculatin forms an ensemble of structurally diverse temporarily functional low-oligomeric pores, which mimic integral membrane protein channels in structure. These pores continuously form and dissociate in the membrane. Membrane permeabilization is dominated by hexa-, hepta- and octamers, which conduct water, ions and small dyes. Pores form by consecutive addition of individual helices to a transmembrane helix or helix bundle, in contrast to current poration models. The diversity of the pore architectures-formed by a single sequence-may be a key feature in preventing bacterial resistance and could explain why sequence-function relationships in AMPs remain elusive.

Indexed as

Amino Acid SequenceAmphibian ProteinsAntimicrobial Cationic PeptidesCircular DichroismLipid BilayersModels, MolecularMolecular Dynamics SimulationProtein BindingProtein ConformationProtein StabilityThermodynamicsAmphibian ProteinsAntimicrobial Cationic PeptidesLipid Bilayersmaculatin-1.1 protein, Litoria

Identifiers

PMID27874004
PMCPMC5121426

What OpenQuestion holds

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Registered trials

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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.