Greenberg S G, Davies P
Department of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5827-31. doi: 10.1073/pnas.87.15.5827.
Paired helical filaments (PHFs) are prominent components of Alzheimer disease (AD) neurofibrillary tangles (NFTs). Rather than isolating NFTs, we selected for PHF populations that can be extracted from AD brain homogenates. About 50% of PHF immunoreactivity can be obtained in 27,200 x g supernatants following homogenization in buffers containing 0.8 M NaCl. We further enriched for PHFs by taking advantage of their insolubility in the presence of zwitterionic detergents and 2-mercaptoethanol, removal of aggregates by filtration through 0.45-microns filters, and sucrose density centrifugation. PHF-enriched fractions contained two to five proteins of 57-68 kDa that displayed the same antigenic properties as PHFs. Since the 57- to 68-kDa PHF proteins are antigenically related to tau proteins, they are similar to the tau proteins previously observed in NFTs. However, further analysis revealed that PHF-associated tau can be distinguished from normal, soluble tau by PHF antibodies that do not recognize human adult tau and by one- and two-dimensional PAGE.
双螺旋丝(PHFs)是阿尔茨海默病(AD)神经原纤维缠结(NFTs)的主要成分。我们没有分离NFTs,而是选择了可从AD脑匀浆中提取的PHF群体。在含有0.8M NaCl的缓冲液中匀浆后,在27,200 x g的上清液中可获得约50%的PHF免疫反应性。我们通过利用它们在两性离子去污剂和2-巯基乙醇存在下的不溶性、通过0.45微米滤器过滤去除聚集体以及蔗糖密度离心进一步富集PHFs。富含PHF的级分含有两到五种57-68 kDa的蛋白质,它们表现出与PHFs相同的抗原特性。由于57至68 kDa的PHF蛋白在抗原上与tau蛋白相关,它们与先前在NFTs中观察到的tau蛋白相似。然而,进一步分析表明,PHF相关的tau可以通过不识别成人tau的PHF抗体以及一维和二维PAGE与正常的可溶性tau区分开来。