Evidence map›Paper›PMID 42330714›Full record

ArticleInternational dental journal2026

Computational Analysis of Antimicrobial Peptides Targeting Agglutinin-Like Protein 3 (Als3) and β-Glucan Synthase in Denture-Associated Candidiasis.

Ravinder S Saini, Doni Dermawan, Shubham Chopra, Rayan Ibrahim H Binduhayyim, Seyed Ali Mosaddad, Mario Alberto Alarcón-Sánchez, Artak Heboyan

Abstract read
In one paragraph

Article in International dental journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

7 authors.

Ravinder S SainiDepartment of Allied Dental Health Sciences COAMS, King Khalid University, Abha, Saudi Arabia.
Doni DermawanFaculty of Chemistry, Applied Biotechnology, Warsaw University of Technology, Warsaw, Poland.
Shubham ChopraMajor in Healthcare, Trinity Western University, Langley, British Columbia, Canada.
Rayan Ibrahim H BinduhayyimDepartment of Allied Dental Health Sciences COAMS, King Khalid University, Abha, Saudi Arabia.
Seyed Ali MosaddadDepartment of Research Analytics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, Tamil Nadu, India; Department of Conservative Dentistry and Bucofacial Prosthesis, Faculty of Odontology, Complutense University of Madrid, Madrid, Spain; Department of Prosthodontics, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: Semosadd@ucm.es.
Mario Alberto Alarcón-SánchezMolecular Biology in Medicine Program, University Center of Health Sciences, University of Guadalajara (CUCS-UdeG), Guadalajara, Jalisco, Mexico; Institute of Research in Dentistry, Department of Integral Dental Clinics, University Center of Health Sciences, University of Guadalajara (CUCS-UdeG), Guadalajara, Jalisco, Mexico.
Artak HeboyanDepartment of Prosthodontics, Faculty of Stomatology, Yerevan State Medical University after Mkhitar Heratsi, Yerevan, Armenia. Electronic address: heboyan.artak@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCandida albicans adhesion and biofilm formation on prosthetic surfaces drive denture-associated candidiasis and are unaffected by traditional fungicidal treatments. Pre-emptive prevention of fungal attachment to prosthetic devices is a rational strategy to avoid recurrent infections.

methodsWe utilized a mechanism-based computational pipeline to screen peptides with activity centred on inhibiting fungal adhesion instead of viability. We chose two colonization-relevant targets: agglutinin-like protein 3 (Als3), involved in surface attachment, and 1,3-β-glucan synthase (GS), involved in glucan-dependent biofilm-support processes. Peptides were ranked using protein-peptide docking, 100-ns molecular dynamics simulations, and MM/PBSA binding free energy calculations to determine metrics of interface coverage, interaction persistence, and dynamic energetic favourability.

resultsWe found that tachystatin consistently and stably occupied the highest proportion of adhesion-related interfaces on both Als3 and GS. Tachystatin dynamics demonstrated lower residue-level fluctuations in functionally relevant residues and preservation of hydrogen bonds throughout the simulation. MM/PBSA assessments revealed favourable and consistent binding energetics facilitated by van der Waals forces. These findings suggest that the peptide may comparatively maintain interface occupancy consistent with a potential steric hindrance effect at adhesion-relevant regions. The selected control peptides failed to occupy the predicted interfaces and demonstrated inadequate stabilities.

conclusionsTargeting Als3-mediated adhesion together with GS-associated biofilm-support processes represent a promising preventive strategy for denture-associated candidiasis. Tachystatin emerged as the most promising peptide within this comparative computational screen and may warrant further evaluation as a candidate for reducing biofilm formation on dental prosthetics Overall, this interaction- and simulation-based framework may support antimicrobial peptide selection focused on biofilm prevention.

Indexed as

Antimicrobial PeptidesCandida albicansCandidiasisFungal ProteinsGlucosyltransferasesBiofilmsHumansMolecular Docking SimulationMolecular Dynamics SimulationALS3 protein, Candida albicansAntimicrobial PeptidesFungal Proteinsglucan synthaseGlucosyltransferases1,3-β-glucan synthaseAls3CandidiasisDenturesMolecular docking

Identifiers

PMID42330714
PMCPMC13315180

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LicenceCC BY-NC-ND
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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.