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- W255289110 abstract "Protein adsorption at liquid-liquid interfaces is of immense relevance to many biological processes and dairy-based functional foods. Due to experimental limitations, however, there is still a remarkable lack of understanding of the adsorption mechanism, particularly at a molecular level. In this study, atomistic molecular dynamics simulations were used to elucidate the approach and adsorption mechanism of β-lactoglobulin (β-LG) at a decane-water interface. Through multiple independent simulations starting from three representative initial orientations of β-LG relative to the decane surface the rate at which β-LG approaches the oil/water interface is found to be independent of its initial orientation, and largely stochastic in nature. While the residues that first make contact with the decane and the final orientation of β-LG upon adsorption are similar in all cases, the adsorption process is driven predominantly by structural rearrangements that preserve the secondary structure but expose hydrophobic residues to the decane surface. This detailed characterization of the adsorption of β-LG at an oil/water interface should inform the design and development of novel encapsulation and delivery systems in the food and pharmaceutical sciences." @default.
- W255289110 created "2016-06-24" @default.
- W255289110 creator A5013534739 @default.
- W255289110 creator A5021362318 @default.
- W255289110 creator A5032082476 @default.
- W255289110 date "2015-05-26" @default.
- W255289110 modified "2023-10-03" @default.
- W255289110 title "Deciphering β-Lactoglobulin Interactions at an Oil–Water Interface: A Molecular Dynamics Study" @default.
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- W255289110 doi "https://doi.org/10.1021/acs.biomac.5b00467" @default.
- W255289110 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25989152" @default.
- W255289110 hasPublicationYear "2015" @default.
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