抗血清
化学
Tau病理学
肽
甲酸
分子生物学
阿尔茨海默病
抗体
生物化学
生物
遗传学
疾病
病理
医学
作者
Jun Kondo,Toshiyuki Honda,Hiroshi Mori,Y. Hamada,Reiko Miura,Midori Ogawara,Yasuo Ihara
出处
期刊:Neuron
[Cell Press]
日期:1988-11-01
卷期号:1 (9): 827-834
被引量:334
标识
DOI:10.1016/0896-6273(88)90130-4
摘要
To obtain definitive evidence that tau is a component of paired helical filaments (PHF) in Alzheimer's disease, we fractionated and sequenced PHF-derived peptides according to a previously described procedure. In the PHF digest, we found four independent tau peptides that were located in the carboxyl third of tau. Subsequent extensive analysis of the PHF digest did not provide any other tau peptides. The conventional PHF antiserum and a new antiserum directed toward formic acid-denatured PHF reacted with the distinct CNBr fragments of tau localized on the carboxy-terminal portion of tau by protein sequencing. From these observations, we conclude that the carboxyl third of tau is tightly bound to PHF.
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