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https://ir.library.oregonstate.edu/concern/articles/5712m829r

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  • Molecular dynamics simulations, conventional and metadynamics, were performed to determine the interaction of model protein Gb1 over kaolinite (001), Na⁺-montmorillonite (001), Ca²⁺-montmorillonite (001), goethite (100), and Na⁺-birnessite (001) mineral surfaces. Gb1, a small (56 residue) protein with a well-characterized solution-state nuclear magnetic resonance (NMR) structure and having α-helix, 4-fold β-sheet, and hydrophobic core features, is used as a model protein to study protein soil mineral interactions and gain insights on structural changes and potential degradation of protein. From our simulations, we observe little change to the hydrated Gb1 structure over the kaolinite, montmorillonite, and goethite surfaces relative to its solvated structure without these mineral surfaces present. Over the Na⁺ -birnessite basal surface, however, the Gb1 structure is highly disturbed as a result of interaction with this birnessite surface. Unraveling of the Gb1 β-sheet at specific turns and a partial unraveling of the α-helix is observed over birnessite, which suggests specific vulnerable residue sites for oxidation or hydrolysis possibly leading to fragmentation.
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  • description.provenance : Approved for entry into archive by Patricia Black(patricia.black@oregonstate.edu) on 2016-07-27T16:10:45Z (GMT) No. of bitstreams: 3 krauserp1074682776.zip: 3800725 bytes, checksum: 544f8dd9b21578f66401150582b90454 (MD5) AndersenProteinMineralInteractions.pdf: 3384214 bytes, checksum: 96eead04d69f3f06628cf5948b3f89b5 (MD5) AndersenProteinMineralInteractionsSupportingInfo.pdf: 958928 bytes, checksum: 040b07ccc9c23b0c73b7dfb5e1214cd4 (MD5)
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