Self‐Assembly of a Conjugate of Lipoic Acid With a Collagen‐Stimulating Pentapeptide Showing Cytocompatibility and Wound Healing Properties, and Chemical and Photolytic Disassembly

Lipoic acid is a biocompatible compound with antioxidant activity that is of considerable interest in cosmetic formulations, and the disulfide group in the N-terminal ring confers redox activity. Here, we study the self-assembly and aspects of the bioactivity of a lipopeptide (peptide amphiphile) comprising the KTTKS collagen-stimulating pentapeptide sequence conjugated to an N-terminal lipoic acid chain, lipoyl-KTTKS. Using SAXS, SANS and cryo-TEM, lipoyl-KTTKS is found to form a population of curly fibrils (wormlike micelles) above a critical aggregation concentration. Upon chemical reduction, the fibrils (and β-sheet structure) are disrupted because of the breaking of the disulfide bond, which produces dihydrolipoic acid. Lipoyl-KTTKS also undergoes photo-degradation in the presence of UV radiation. Through cell assays using fibroblasts, we found that lipoyl-KTTKS has excellent cytocompatibility across a wide concentration range, stimulates collagen production, and enhances the rate of cell coverage in a simple in vitro scratch assay of 'wound healing'. Lipoyl-KTTKS thus has several notable properties that may be useful for the development of cosmetics, cell scaffolds or tissue engineering materials.

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Publication Details

Journal
Journal of Peptide Science
Published
2025-02-04
DOI
https://doi.org/10.1002/psc.70002
Citations
3
Primary Topic
Biochemical Acid Research Studies
Type
article
Field-Weighted Citation Impact
3.34

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article

Self‐Assembly of a Conjugate of Lipoic Acid With a Collagen‐Stimulating Pentapeptide Showing Cytocompatibility and Wound Healing Properties, and Chemical and Photolytic Disassembly

Leide Passos Cavalcanti, Ian W. Hamley, Jani Seitsonen, Valeria Castelletto et al.
3 citations
Journal of Peptide Science
Biochemical Acid Research Studies
3.34
article

Self‐Assembly of a Conjugate of Lipoic Acid With a Collagen‐Stimulating Pentapeptide Showing Cytocompatibility and Wound Healing Properties, and Chemical and Photolytic Disassembly

Leide Passos Cavalcanti, Ian W. Hamley, Jani Seitsonen, Valeria Castelletto, Lucas R. de Mello
article en
3 citations

Abstract

Lipoic acid is a biocompatible compound with antioxidant activity that is of considerable interest in cosmetic formulations, and the disulfide group in the N-terminal ring confers redox activity. Here, we study the self-assembly and aspects of the bioactivity of a lipopeptide (peptide amphiphile) comprising the KTTKS collagen-stimulating pentapeptide sequence conjugated to an N-terminal lipoic acid chain, lipoyl-KTTKS. Using SAXS, SANS and cryo-TEM, lipoyl-KTTKS is found to form a population of curly fibrils (wormlike micelles) above a critical aggregation concentration. Upon chemical reduction, the fibrils (and β-sheet structure) are disrupted because of the breaking of the disulfide bond, which produces dihydrolipoic acid. Lipoyl-KTTKS also undergoes photo-degradation in the presence of UV radiation. Through cell assays using fibroblasts, we found that lipoyl-KTTKS has excellent cytocompatibility across a wide concentration range, stimulates collagen production, and enhances the rate of cell coverage in a simple in vitro scratch assay of 'wound healing'. Lipoyl-KTTKS thus has several notable properties that may be useful for the development of cosmetics, cell scaffolds or tissue engineering materials.

Journal of Peptide ScienceVol. 31(3)
Rutherford Appleton Laboratory (GB), Science and Technology Facilities Council (GB), University of Reading (GB), Aalto University (FI)
University of Reading, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 10%
Biochemical Acid Research Studies
3.34
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Self‐Assembly of a Conjugate of Lipoic Acid With a Collagen‐Stimulating Pentapeptide Showing Cytocompatibility and Wound Healing Properties, and Chemical and Photolytic Disassembly — Leide Passos Cavalcanti, Ian W. Hamley, et al. · Journal of Peptide Science (2025) | TGRS Research Map | TGRS