Evidence map›Paper›PMID 34251525›Full record

ArticleAmino acids2021

Membrane interactions of Ocellatins. Where do antimicrobial gaps stem from?

José Muñoz-López, Jade C L Oliveira, Daniel A G R Michel, Carolina S Ferreira, Francisco Gomes Neto, Evgeniy S Salnikov, Rodrigo M Verly, Burkhard Bechinger, Jarbas M Resende

Abstract read
PubMed Publisher
In one paragraph

Article in Amino acids, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Comparative Structural and Biophysical Investigation ofAntibiotics (Basel, Switzerland) · 2025
    Article
  3. 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

9 authors at 4 institutions in 2 countries.

José Muñoz-LópezDepartamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, P.O. Box 486, Belo Horizonte, MG, 31270-901, Brazil.
Jade C L OliveiraDepartamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, P.O. Box 486, Belo Horizonte, MG, 31270-901, Brazil.
Daniel A G R MichelDepartamento de Química, Universidade Federal Dos Vales do Jequitinhonha e Mucuri, Diamantina, MG, 39100-000, Brazil.
Carolina S FerreiraDepartamento de Química, Universidade Federal Dos Vales do Jequitinhonha e Mucuri, Diamantina, MG, 39100-000, Brazil.
Francisco Gomes NetoLaboratório de Toxinologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, 21040-900, Brazil.
Evgeniy S SalnikovUMR7177, Institut de Chimie, Université de Strasbourg/CNRS, 4, rue Blaise Pascal , 67000, Strasbourg, France.
Rodrigo M VerlyDepartamento de Química, Universidade Federal Dos Vales do Jequitinhonha e Mucuri, Diamantina, MG, 39100-000, Brazil.
Burkhard BechingerUMR7177, Institut de Chimie, Université de Strasbourg/CNRS, 4, rue Blaise Pascal , 67000, Strasbourg, France.
Jarbas M ResendeDepartamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, P.O. Box 486, Belo Horizonte, MG, 31270-901, Brazil. jmr@ufmg.br.
Universidade Federal de Minas Gerais · BRUniversidade Federal dos Vales do Jequitinhonha e Mucuri · BRCentre National de la Recherche Scientifique · FRFundação Oswaldo Cruz · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 311391/2020-6Conselho Nacional de Desenvolvimento Científico e Tecnológico 312418/2017-5
6 · The paper itself

Abstract

The antimicrobial peptides Ocellatin-LB1, -LB2 and -F1, isolated from frogs, are identical from residue 1 to 22, which correspond to the -LB1 sequence, whereas -LB2 carries an extra N and -F1 additional NKL residues at their C-termini. Despite the similar sequences, previous investigations showed different spectra of activities and biophysical investigations indicated a direct correlation between both membrane-disruptive properties and activities, i.e., ocellatin-F1 > ocellatin-LB1 > ocellatin-LB2. This study presents experimental evidence as well as results from theoretical studies that contribute to a deeper understanding on how these peptides exert their antimicrobial activities and how small differences in the amino acid composition and their secondary structure can be correlated to these activity gaps. Solid-state NMR experiments allied to the simulation of anisotropic NMR parameters allowed the determination of the membrane topologies of these ocellatins. Interestingly, the extra Asn residue at the Ocellatin-LB2 C-terminus results in increased topological flexibility, which is mainly related to wobbling of the helix main axis as noticed by molecular dynamics simulations. Binding kinetics and thermodynamics of the interactions have also been assessed by Surface Plasmon Resonance and Isothermal Titration Calorimetry. Therefore, these investigations allowed to understand in atomic detail the relationships between peptide structure and membrane topology, which are in tune within the series -F1 >  > -LB1 ≥ -LB2, as well as how peptide dynamics can affect membrane topology, insertion and binding.

Indexed as

AnimalsAntimicrobial Cationic PeptidesAnuraCalorimetryCell MembraneKineticsMagnetic Resonance SpectroscopyMolecular Dynamics SimulationSurface Plasmon ResonanceThermodynamicsAntimicrobial Cationic PeptidesAmphipathic peptideAntimicrobial peptidesMembrane peptide dynamicsOcellatinsPeptide–membrane interactionsSolid-state NMR spectroscopy

Identifiers

PMID34251525
OpenAlexW3183032281

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.