Evidence map›Paper›PMID 40806517›Full record

ArticleInternational journal of molecular sciences2025

Computational Design of Potentially Multifunctional Antimicrobial Peptide Candidates via a Hybrid Generative Model.

Fangli Ying, Wilten Go, Zilong Li, Chaoqian Ouyang, Aniwat Phaphuangwittayakul, Riyad Dhuny

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Review
  2. Review
  3. Review
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

6 authors.

Fangli YingDepartment of Computer Science and Engineering, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.ORCID 0000-0001-8390-3229
Wilten GoDepartment of Computer Science and Engineering, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.
Zilong LiDepartment of Computer Science and Engineering, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.
Chaoqian OuyangDepartment of Computer Science and Engineering, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.
Aniwat PhaphuangwittayakulInternational College of Digital Innovation, Chiang Mai University, Chiang Mai 50200, Thailand.ORCID 0000-0002-2289-3116
Riyad DhunyDepartment of Creative Arts, Film and Media Technologies, University of Technology, Mauritius, La Tour Koenig, Pointe-aux-Sables 11134, Mauritius.ORCID 0000-0003-4779-0268

Funding

Key R&D Program of Shandong Province, China 2022SFGC0104
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) provide a robust alternative to conventional antibiotics, combating escalating microbial resistance through their diverse functions and broad pathogen-targeting abilities. While current deep learning technologies enhance AMP generation, they face challenges in developing multifunctional AMPs due to intricate amino acid interdependencies and limited consideration of diverse functional activities. To overcome this challenge, we introduce a novel de novo multifunctional AMP design framework that enhances a Feedback Generative Adversarial Network (FBGAN) by integrating a global quantitative AMP activity regression module and a multifunctional-attribute integrated prediction module. This integrated approach not only facilitates the automated generation of potential AMP candidates, but also optimizes the network's ability to assess their multifunctionality. Initially, by integrating an effective pre-trained regression and classification model with feedback-loop mechanisms, our model can not only identify potential valid AMP candidates, but also optimizes computational predictions of Minimum Inhibitory Concentration (MIC) values. Subsequently, we employ a combinatorial predictor to simultaneously identify and predict five multifunctional AMP bioactivities, enabling the generation of multifunctional AMPs. The experimental results demonstrate the efficiency of generating AMPs with multiple enhanced antimicrobial properties, indicating that our work can provide a valuable reference for combating multi-drug-resistant infections.

Indexed as

Antimicrobial PeptidesComputational BiologyDrug DesignAnti-Bacterial AgentsMicrobial Sensitivity TestsAnti-Bacterial AgentsAntimicrobial Peptidesantimicrobial peptidesDeep Generative ModelsGANs

Identifiers

PMID40806517
PMCPMC12347886

What OpenQuestion 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 OpenQuestion graph.