Characterization of mAb AP422, a novel phosphorylation-dependent monoclonal antibody against tan protein

被引:151
作者
Hasegawa, M
Jakes, R
Crowther, RA
Lee, VMY
Ihara, Y
Goedert, M
机构
[1] MRC,MOLEC BIOL LAB,CAMBRIDGE CB2 2QH,ENGLAND
[2] UNIV TOKYO,BRAIN RES INST,DEPT NEUROPATHOL,BUNKYO KU,TOKYO 113,JAPAN
[3] UNIV PENN,SCH MED,DEPT PATHOL & LAB MED,PHILADELPHIA,PA 19104
关键词
tau protein; phosphorylation; MAP kinase; Alzheimer's disease;
D O I
10.1016/0014-5793(96)00271-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A monoclonal antibody (AP422) specific for phosphoserine 422 in microtubule-associated protein tau has been produced, It strongly labels paired helical filament (PHF) tau from Alzheimer's disease brain in a phosphorylation-dependent manner, By contrast, AP422 only labels a small fraction of fetal tau and a very small fraction of tau from adult brain, The amount of tan phosphorylated at Ser-422 in normal brain is minor relative to that phosphorylated at sites recognized by other phosphorylation-dependent anti-tau antibodies of known epitope. It follows that AP422 is the most specific anti-tau antibody available for detecting the neurofibrillary lesions of Alzheimer's disease, We also show that Ser-422 in tau is a good in vitro substrate for mitogen-activated protein kinase, but not for glycogen synthase kinase-3 or neuronal cdc2-like kinase.
引用
收藏
页码:25 / 30
页数:6
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