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Importance of local structures of second and third repeat fragments of microtubule-binding domain for tau filament formation
Authors:Tokimasa Mari  Minoura Katsuhiko  Hiraoka Shuko  Tomoo Koji  Sumida Miho  Taniguchi Taizo  Ishida Toshimasa
Institution:Department of Physical Chemistry, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.
Abstract:To investigate the importance of the seventh residue of the second and third repeat fragments (R2 and R3 peptides) of the microtubule-binding domain (MBD) for tau filamentous assembly, the residues Lys and Pro were substituted (R2-K7P and R3-P7K). The filament formations of the R2 and R3 peptides were almost lost due to their substitutions despite their overall conformational similarities. The NOE analyses showed the importance of the conformational flexibility for the R2 peptide and the coupled extended and helical conformations for the R3 peptide in their limited N-terminal regions around their seventh residues. The result shows that the filament formation of MBD is initiated from a short fragment region containing the minimal conformational or functional motif.
Keywords:AD  Alzheimer’s disease  MBD  microtubule-binding domain  MT  microtubule  NFT  neurofibrillary tangle  NOESY  nuclear Overhauser effect spectroscopy  NOE  nuclear Overhauser effect  PHF  paired helical filament  TFA  trifluoroacetic acid  TFE  trifluoroethanol  ThS  thioflavin S  TOCSY  total correlation spectroscopy  TSP  3-(trimethylsilyl)propionic acid
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