Molecular DynamicsStudy on the Influence of the CLKMotif on the Structural Stability of Collagen-Like Peptides Adsorbedon Gold Nanosurfaces

The role of the cysteine–leucine–lysine (CLK) motif in enhancing the structural stability of collagen-like peptides (CLPs) adsorbed onto gold nanosurfaces is investigated in this study. The effects of CLK inclusion in CLPs on peptide adsorption, structural stability, and hydrogen bonding behavior in both solvent and surface environments are analyzed by using molecular dynamics simulations. It is shown that CLPs containing the CLK motif (P1-CLK) exhibit stronger binding, greater water displacement, and more stable conformations compared to non-modified CLPs (P1). Additionally, energetically favorable behavior is observed in simulations with multiple peptides, leading to enhanced surface coverage for P1-CLK. These findings indicate that the CLK motif is crucial for optimizing peptide-surface interactions with potential applications in biomaterials design.

Publication Details

Journal
Figshare
Published
2025-03-06
DOI
https://doi.org/10.1021/acsomega.4c10450.s001
Primary Topic
Collagen: Extraction and Characterization
Type
article
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article

Molecular DynamicsStudy on the Influence of the CLKMotif on the Structural Stability of Collagen-Like Peptides Adsorbedon Gold Nanosurfaces

Figshare
Collagen: Extraction and Characterization
article

Molecular DynamicsStudy on the Influence of the CLKMotif on the Structural Stability of Collagen-Like Peptides Adsorbedon Gold Nanosurfaces

article en

Abstract

The role of the cysteine–leucine–lysine (CLK) motif in enhancing the structural stability of collagen-like peptides (CLPs) adsorbed onto gold nanosurfaces is investigated in this study. The effects of CLK inclusion in CLPs on peptide adsorption, structural stability, and hydrogen bonding behavior in both solvent and surface environments are analyzed by using molecular dynamics simulations. It is shown that CLPs containing the CLK motif (P1-CLK) exhibit stronger binding, greater water displacement, and more stable conformations compared to non-modified CLPs (P1). Additionally, energetically favorable behavior is observed in simulations with multiple peptides, leading to enhanced surface coverage for P1-CLK. These findings indicate that the CLK motif is crucial for optimizing peptide-surface interactions with potential applications in biomaterials design.

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Openalex Percentile: Top 69%
Collagen: Extraction and Characterization
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