Evidence map›Paper›PMID 39005792›Full record

ArticleACS omega2024

Anti-Staphy Peptides Rationally Designed from Cry10Aa Bacterial Protein.

Thuanny Borba Rios, Mariana Rocha Maximiano, Fabiano Cavalcanti Fernandes, Gabriella Cavalcante Amorim, William Farias Porto, Danieli Fernanda Buccini, Valentina Nieto Marín, Gabriel Cidade Feitosa, Carlos Daniel Pereira Freitas, Juliana Bueno Barra and 4 more

Abstract read
In one paragraph

Article in ACS omega, 2024. 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
–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

3 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Thuanny Borba RiosS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia Universidade Católica Dom Bosco, Av. Tamandaré, 6000-Jardim Seminario, Campo Grande, MS 79117-900, Brazil.
Mariana Rocha MaximianoS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia Universidade Católica Dom Bosco, Av. Tamandaré, 6000-Jardim Seminario, Campo Grande, MS 79117-900, Brazil.
Fabiano Cavalcanti FernandesCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia Universidade Católica de Brasília, St. de Grandes Áreas Norte 916-Asa Norte, Brasília, DF 70790-160, Brazil.
Gabriella Cavalcante AmorimCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia Universidade Católica de Brasília, St. de Grandes Áreas Norte 916-Asa Norte, Brasília, DF 70790-160, Brazil.
William Farias PortoPorto Reports, Brasília, DF 70770-917, Brazil.
Danieli Fernanda BucciniS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia Universidade Católica Dom Bosco, Av. Tamandaré, 6000-Jardim Seminario, Campo Grande, MS 79117-900, Brazil.
Valentina Nieto MarínS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia Universidade Católica Dom Bosco, Av. Tamandaré, 6000-Jardim Seminario, Campo Grande, MS 79117-900, Brazil.
Gabriel Cidade FeitosaCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia Universidade Católica de Brasília, St. de Grandes Áreas Norte 916-Asa Norte, Brasília, DF 70790-160, Brazil.
Carlos Daniel Pereira FreitasLaboratório de RMN, Instituto de Química, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil.
Juliana Bueno BarraLaboratório de RMN, Instituto de Química, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil.
Antonio AlonsoInstituto de Física, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil.
Maria Fátima Grossi de SáCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia Universidade Católica de Brasília, St. de Grandes Áreas Norte 916-Asa Norte, Brasília, DF 70790-160, Brazil.
Luciano Morais LiãoLaboratório de RMN, Instituto de Química, Universidade Federal de Goiás, Goiânia, GO 74690-900, Brazil.ORCID https://orcid.org/0000-0001-9985-2980
Octávio Luiz FrancoS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia Universidade Católica Dom Bosco, Av. Tamandaré, 6000-Jardim Seminario, Campo Grande, MS 79117-900, Brazil.ORCID https://orcid.org/0000-0001-9546-0525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial infections pose a significant threat to human health, constituting a major challenge for healthcare systems. Antibiotic resistance is particularly concerning in the context of treating staphylococcal infections. In addressing this challenge, antimicrobial peptides (AMPs), characterized by their hydrophobic and cationic properties, unique mechanism of action, and remarkable bactericidal and immunomodulatory capabilities, emerge as promising alternatives to conventional antibiotics for tackling bacterial multidrug resistance. This study focuses on the Cry10Aa protein as a template for generating AMPs due to its membrane-penetrating ability. Leveraging the Joker algorithm, six peptide variants were derived from α-helix 3 of Cry10Aa, known for its interaction with lipid bilayers. In vitro, antimicrobial assays determined the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) required for inhibiting the growth of

Identifiers

PMID39005792
PMCPMC11238290

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.