Microtubule-associated protein tau. A component of Alzheimer paired helical filaments.

Inge Grundke‐Iqbal(New York State Office for People With Developmental Disabilities), Khalid Iqbal(New York State Office for People With Developmental Disabilities), M Quinlan(New York State Office for People With Developmental Disabilities), Y C Tung(New York State Office for People With Developmental Disabilities), Mariem Zaidi(New York State Office for People With Developmental Disabilities), H. M. Wiśniewski(New York State Office for People With Developmental Disabilities)
Journal of Biological Chemistry
May 1, 1986
Cited by 1,771Open Access
Full Text

Abstract

Microtubule-associated protein tau was purified from bovine brain microtubules by either (1) phosphocellulose chromatography, (2) heat treatment at pH 6.4, (3) heat treatment at pH 2.7, (4) heat treatment at pH 2.7 followed by extraction with perchloric acid and precipitation with glycerol, or (5) by precipitation with ammonium sulfate followed by extraction with perchloric acid. All of these tau preparations reacted specifically with antibodies to Alzheimer paired helical filaments. Affinity purified antibodies to tau labeled both Alzheimer neurofibrillary tangles and plaque neurites but not amyloid in Alzheimer brain tissue sections and labeled paired helical filament polypeptides on Western blots. Human brain tau and paired helical filament polypeptides co-migrated on sodium dodecyl sulfate-polyacrylamide gels. These results suggest that tau is a major component of Alzheimer paired helical filaments.


Related Papers

No related papers found

Powered by citation graph analysis