TAU FIBRIL WITH MEMBRANE LIPIDS: INSIGHT FROM COMPUTATIONAL MODELING AND SIMULATIONS

dc.contributor.authorBarredo, Prechiel A.
dc.contributor.authorFernandez, Marvin Jose F.
dc.contributor.authorAmbe, Christopher E.
dc.contributor.authorBalanay, Mannix P.
dc.date.accessioned2022-11-29T10:24:00Z
dc.date.available2022-11-29T10:24:00Z
dc.date.issued2021-10-15
dc.description.abstractThe microtubule-binding protein tau has been the center of researches concerning Alzheimer’s disease (AD) due to several clinical trials of β-amyloid therapies failing recently. The availability of the tau fibril structure from AD brain enables computational modeling studies to calculate binding affinities with different ligands. In this study, the tau paired helical filaments (PHF-Tau) (PDB ID: 5O3L) was used as receptor and interactions with the lipids: 3- alpha-cholesterol; 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine; and C18:1 sphingomyelin, were explored with molecular docking, molecular dynamics, and natural bond orbital analysis. Docking sites upon solvation of the protein with transferable interatomic potential- 3 points reveal the amphipathic nature of PHF-Tau and molecular dynamics simulations show that the embedded phosphocholine at the tail side gives high potential energy values with some amino acids forming H-bond interactions.en_US
dc.identifier.citationBarredo, P. A., Fernandez, M. J. F., Ambe, C. E., & Balanay, M. P. (2021). Tau fibril with membrane lipids: Insight from computational modeling and simulations. PLOS ONE, 16(10), e0258692. https://doi.org/10.1371/journal.pone.0258692en_US
dc.identifier.urihttp://nur.nu.edu.kz/handle/123456789/6837
dc.language.isoenen_US
dc.publisherPLOS ONEen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.subjectType of access: Open Accessen_US
dc.subjectmembrane lipidsen_US
dc.subjectTau fibrilen_US
dc.titleTAU FIBRIL WITH MEMBRANE LIPIDS: INSIGHT FROM COMPUTATIONAL MODELING AND SIMULATIONSen_US
dc.typeArticleen_US
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