Evidence map›Paper›PMID 39201537›Full record

ArticleInternational journal of molecular sciences2024

Protein Language Models and Machine Learning Facilitate the Identification of Antimicrobial Peptides.

David Medina-Ortiz, Seba Contreras, Diego Fernández, Nicole Soto-García, Iván Moya, Gabriel Cabas-Mora, Álvaro Olivera-Nappa

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Peptipedia v2.0: a peptide sequence database and user-friendly web platform. A major update.Database : the journal of biological databases and curation · 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

7 authors.

David Medina-OrtizDepartamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210005, Chile.ORCID 0000-0002-8369-5746
Seba ContrerasMax Planck Institute for Dynamics and Self-Organization, Am Faßberg 17, 37077 Göttingen, Germany.ORCID 0000-0001-8909-774X
Diego FernándezDepartamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210005, Chile.
Nicole Soto-GarcíaDepartamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210005, Chile.ORCID 0009-0001-1438-1938
Iván MoyaDepartamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210005, Chile.ORCID 0000-0002-0458-378X
Gabriel Cabas-MoraDepartamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210005, Chile.ORCID 0009-0004-2344-9860
Álvaro Olivera-NappaCentre for Biotechnology and Bioengineering, CeBiB, Universidad de Chile, Santiago 8370456, Chile.ORCID 0000-0001-6053-7019

Funding

Agencia Nacional de Investigación y Desarrollo PIA project FB0001Agencia Nacional de Investigación y Desarrollo ``SUBVENCION A INSTALACION EN LA ACADEMIA CONVOCATORIA ANO 2022", Folio 85220004Max Planck Society NA
6 · The paper itself

Abstract

Peptides are bioactive molecules whose functional versatility in living organisms has led to successful applications in diverse fields. In recent years, the amount of data describing peptide sequences and function collected in open repositories has substantially increased, allowing the application of more complex computational models to study the relations between the peptide composition and function. This work introduces AMP-Detector, a sequence-based classification model for the detection of peptides' functional biological activity, focusing on accelerating the discovery and de novo design of potential antimicrobial peptides (AMPs). AMP-Detector introduces a novel sequence-based pipeline to train binary classification models, integrating protein language models and machine learning algorithms. This pipeline produced 21 models targeting antimicrobial, antiviral, and antibacterial activity, achieving average precision exceeding 83%. Benchmark analyses revealed that our models outperformed existing methods for AMPs and delivered comparable results for other biological activity types. Utilizing the Peptide Atlas, we applied AMP-Detector to discover over 190,000 potential AMPs and demonstrated that it is an integrative approach with generative learning to aid in de novo design, resulting in over 500 novel AMPs. The combination of our methodology, robust models, and a generative design strategy offers a significant advancement in peptide-based drug discovery and represents a pivotal tool for therapeutic applications.

Indexed as

Antimicrobial PeptidesMachine LearningAlgorithmsAmino Acid SequenceAntimicrobial Cationic PeptidesComputational BiologyDrug DiscoveryAntimicrobial Cationic PeptidesAntimicrobial Peptidesantimicrobial peptidesgenerative learningmachine learningpeptide designpeptide discoveryprotein language models

Identifiers

PMID39201537
PMCPMC11487388

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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.