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- W2893184077 abstract "Abstract Microtubule‐associated Tau protein plays a key role in assembling microtubule and modulating the functional organization of the neuron and developing axonal morphology, growth, and polarity. The pathological Tau can aggregate into cross‐beta amyloid as one of the hallmarks for Alzheimer's disease (AD). Therefore, one of the top priorities in AD research is to figure out the structural model of Tau aggregation and to screen the inhibitors. The latest generation intrinsically disordered protein specific force field ff 14IDPSFF significantly improved the distributions of heterogeneous conformations for intrinsically disordered proteins (IDPs). Here, the molecular dynamics (MD) simulations with three force fields of ff 14SB, ff 14IDPs, and ff 14IDPSFF were employed to investigate the secondary structures transition of Tau (267–312) fragment. The results indicate that ff 14IDPSFF can generate more heterogeneous conformers, and the predicted secondary structural distribution is closer to that of the experimental observation. In addition, predicted secondary chemical shifts from ff 14IDPSFF are the most approach to those of experiment. Secondary structures transition kinetics for Tau(267–312) with ff 14IDPSFF shows that the secondary structures were gradually transformed from α‐helix to β‐strand and the β‐strand located at the regions of the residues 274–280 and residues 305–311. Besides, the driving force for the secondary structures transition of Tau(267–312) is mainly hydrophobic interactions which located at hexa‐peptides 275 VQIINK 280 and 306 VQIVYK 311 . Secondary structure transition of Tau protein can give insight into the aggregation mechanism for AD." @default.
- W2893184077 created "2018-10-05" @default.
- W2893184077 creator A5065011685 @default.
- W2893184077 creator A5086992948 @default.
- W2893184077 date "2018-10-17" @default.
- W2893184077 modified "2023-10-14" @default.
- W2893184077 title "Secondary structures transition of tau protein with intrinsically disordered proteins specific force field" @default.
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- W2893184077 doi "https://doi.org/10.1111/cbdd.13407" @default.
- W2893184077 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30259679" @default.
- W2893184077 hasPublicationYear "2018" @default.
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