Tokimasa Mari, Minoura Katsuhiko, Hiraoka Shuko, Tomoo Koji, Sumida Miho, Taniguchi Taizo, Ishida Toshimasa
Department of Physical Chemistry, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.
FEBS Lett. 2005 Jul 4;579(17):3481-6. doi: 10.1016/j.febslet.2005.05.020.
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.
为了研究微管结合域(MBD)的第二个和第三个重复片段(R2和R3肽段)的第七个残基对tau丝状组装的重要性,将赖氨酸(Lys)和脯氨酸(Pro)残基进行了替换(R2-K7P和R3-P7K)。尽管R2和R3肽段的整体构象相似,但由于它们的替换,其丝状形成几乎丧失。NOE分析表明,R2肽段构象灵活性以及R3肽段在其第七个残基周围有限的N端区域中的耦合延伸和螺旋构象的重要性。结果表明,MBD的丝状形成是从包含最小构象或功能基序的短片段区域开始的。