TAU-2 - A PROBE FOR A SER CONFORMATION IN THE AMINO TERMINUS OF TAU

被引:49
作者
WATANABE, N
TAKIO, K
HASEGAWA, M
ARAI, T
TITANI, K
IHARA, Y
机构
[1] UNIV TOKYO,FAC MED,INST BRAIN RES,DEPT NEUROPATHOL,7-3-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
[2] SCI UNIV TOKYO,FAC SCI & TECHNOL,DEPT APPL BIOL SCI,NODA,CHIBA 278,JAPAN
[3] RIKEN,AGING PROC RES LAB,FRONTIER RES PROGRAM,WAKO,JAPAN
[4] FUJITA HLTH UNIV,SCH MED,INST COMPREHENS MED SCI,DIV BIOMED POLYMER SCI,TOYOAKE,JAPAN
[5] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,DEPT NEUROPHYSIOL,TOKYO 173,JAPAN
关键词
ALZHEIMERS DISEASE; PAIRED HELICAL FILAMENTS; TAU; TAU-2; EPITOPE MAPPING;
D O I
10.1111/j.1471-4159.1992.tb09349.x
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
We have determined the epitope for Tau 2, a monoclonal antibody that intensely stained tangles, plaque neurites, and curly fibers in the tissue section, and strongly labeled bovine tau, but only very weakly labeled human tau on the blot. The epitope has been localized to Ala95 through Ala108 of bovine tau. Ser101 is critical for Tau 2 reactivities; the replacement of Ser by Pro, which is found in rat, mouse, and human tau, brings about very weak Tau 2 reactivities. The strong Tau 2 staining of tangles and its effective absorption with a synthetic Ser peptide (Ala95 through Ala108) suggest that the tau in paired helical filaments takes a Ser conformation, rather than a Pro conformation, in its amino-terminal portion.
引用
收藏
页码:960 / 966
页数:7
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