Evidence map›Paper›PMID 35359712›Full record

ArticleFrontiers in microbiology2022

The Screen of a Phage Display Library Identifies a Peptide That Binds to the Surface of

Jéssica I de Paula, Eduardo J Lopes-Torres, Marcelo Jacobs-Lorena, Marcia Cristina Paes, Sung-Jae Cha

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Peptide selection via phage display to inhibitFrontiers in microbiology · 2024
    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 3 institutions in 2 countries.

Jéssica I de PaulaLaboratório de Interação Tripanossomatídeos e Vetores - Departamento de Bioquímica, IBRAG - UERJ, Rio de Janeiro, Brazil.
Eduardo J Lopes-TorresLaboratório de Helmintologia Romero Lascasas Porto, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
Marcelo Jacobs-LorenaJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology and Malaria Research Institute, Baltimore, MD, United States.
Marcia Cristina PaesLaboratório de Interação Tripanossomatídeos e Vetores - Departamento de Bioquímica, IBRAG - UERJ, Rio de Janeiro, Brazil.
Sung-Jae ChaJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology and Malaria Research Institute, Baltimore, MD, United States.
Johns Hopkins University · USInstituto Nacional de Ciência e Tecnologia em Entomologia Molecular · BRUniversidade do Estado do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chagas is a neglected tropical disease caused by the protozoan parasite Methods: Three selection rounds of a phage peptide display library for isolation of phages that bind to trypomastigotes, resulted in the identification of the N3 dodecapeptide. N3 peptide binding to Results: Phage display screening identified the N3 peptide that binds preferentially to the surface of the trypomastigote and amastigote infective forms as opposed to non-infective epimastigotes. Importantly, the N3 peptide, but not a control scrambled peptide, inhibits trypomastigote invasion of Vero cells by 50%. Conclusion: The N3 peptide specifically binds to

Indexed as

infectionpeptide libraryphage displayTrypanosoma cruzitrypomastigote

Identifiers

PMID35359712
PMCPMC8960960
OpenAlexW4220731492

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.