Bioactive peptide matrikines: discovery approaches for skin rejuvenation

Aging of human skin is driven in part by cumulative damage to extracellular matrix (ECM) proteins, resulting in wrinkles, laxity, and reduced capacity to heal. Bioactive peptide matrikines are promising therapeutic agents capable of stimulating ECM regeneration and remodeling. This review focuses on how the discovery strategies to identify these peptides have evolved over several decades of cosmeceutical use. Early peptide matrikines were identified primarily through repetitive in vitro testing, based on prior knowledge of a protein or functional region. More recently, there is a focus on in silico prediction of bioactive peptide sequences, implementing techniques such as protease cleavage prediction, protein sequence motif screening, molecular docking, and machine learning algorithms to rapidly derive peptide candidates in silico. We highlight our recently developed in silico to in vivo discovery pipeline, which integrates prediction of aging-related cleavage susceptibility of ECM proteins with comprehensive in vitro and in vivo testing, culminating in the identification of two tetrapeptides (pal-GPKG and pal-LSVD) which act synergistically to enhance ECM regeneration in aged skin. Looking forward, advances in deep learning cleavage prediction models, molecular modeling, and in vitro testing with three-dimensional (3-D) skin models will accelerate the discovery and translation of novel matrikines for skin regeneration and broader biomedical applications, such as wound repair.

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Publication Details

Journal
American Journal of Physiology-Cell Physiology
Published
2026-03-02
DOI
https://doi.org/10.1152/ajpcell.00881.2025
Primary Topic
Antimicrobial Peptides and Activities
Type
article
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article

Bioactive peptide matrikines: discovery approaches for skin rejuvenation

Alexander Eckersley, Matiss Ozols, Michael J. Sherratt, Zeyad El-Houni et al.
American Journal of Physiology-Cell Physiology
Antimicrobial Peptides and Activities
article

Bioactive peptide matrikines: discovery approaches for skin rejuvenation

Alexander Eckersley, Matiss Ozols, Michael J. Sherratt, Zeyad El-Houni, Joe Swift, Krishan Mistry, Tess Birtles, Mike Bell, Eleanor J Bradley
article en

Abstract

Aging of human skin is driven in part by cumulative damage to extracellular matrix (ECM) proteins, resulting in wrinkles, laxity, and reduced capacity to heal. Bioactive peptide matrikines are promising therapeutic agents capable of stimulating ECM regeneration and remodeling. This review focuses on how the discovery strategies to identify these peptides have evolved over several decades of cosmeceutical use. Early peptide matrikines were identified primarily through repetitive in vitro testing, based on prior knowledge of a protein or functional region. More recently, there is a focus on in silico prediction of bioactive peptide sequences, implementing techniques such as protease cleavage prediction, protein sequence motif screening, molecular docking, and machine learning algorithms to rapidly derive peptide candidates in silico. We highlight our recently developed in silico to in vivo discovery pipeline, which integrates prediction of aging-related cleavage susceptibility of ECM proteins with comprehensive in vitro and in vivo testing, culminating in the identification of two tetrapeptides (pal-GPKG and pal-LSVD) which act synergistically to enhance ECM regeneration in aged skin. Looking forward, advances in deep learning cleavage prediction models, molecular modeling, and in vitro testing with three-dimensional (3-D) skin models will accelerate the discovery and translation of novel matrikines for skin regeneration and broader biomedical applications, such as wound repair.

American Journal of Physiology-Cell PhysiologyVol. 330(4)
Wellcome Sanger Institute (GB), University of Manchester (GB), BOE Technology Group (China) (CN)
Openalex Percentile: Top 37%
Antimicrobial Peptides and Activities
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Bioactive peptide matrikines: discovery approaches for skin rejuvenation — Alexander Eckersley, Matiss Ozols, et al. · American Journal of Physiology-Cell Physiology (2026) | TGRS Research Map | TGRS