Miyata Y, Hoshi M, Nishida E, Minami Y, Sakai H
J Biol Chem. 1986 Oct 5;261(28):13026-30.
Two major brain microtubule-associated proteins (MAPs), MAP2 and tau, were found to bind to the intermediate filaments reassembled from neurofilament 70-kDa subunit protein (= 70-kDa filaments). The binding was saturable. The apparent dissociation constant (KD) for the binding of MAP2 to the 70-kDa filaments was estimated to be 4.8 X 10(-7) M, and the maximum binding reached 1 mol of MAP2/approximately 30 mol of 70-kDa protein. The apparent KD for the tau binding was 1.6 X 10(-6) M, and the maximum binding was 1 mol of tau/approximately 3 mol of 70-kDa protein. It was also found that MAP2 and tau did not compete with each other for binding to the 70-kDa filaments. Most interestingly, calmodulin, a ubiquitous Ca2+-binding protein in eukaryotic cells, was found to inhibit the binding of MAP2 and tau to the 70-kDa filaments. The inhibition by calmodulin was regulated by changes in Ca2+ concentration around 10(-6) M, and was canceled by trifluoperazine, a calmodulin inhibitor.
人们发现两种主要的脑微管相关蛋白(MAPs),即MAP2和tau,能与由神经丝70-kDa亚基蛋白重新组装而成的中间丝结合(= 70-kDa丝)。这种结合是可饱和的。MAP2与70-kDa丝结合的表观解离常数(KD)估计为4.8×10⁻⁷ M,最大结合量达到1摩尔MAP2/约30摩尔70-kDa蛋白。tau结合的表观KD为1.6×10⁻⁶ M,最大结合量为1摩尔tau/约3摩尔70-kDa蛋白。还发现MAP2和tau在与70-kDa丝的结合上并不相互竞争。最有趣的是,钙调蛋白是真核细胞中一种普遍存在的Ca²⁺结合蛋白,它能抑制MAP2和tau与70-kDa丝的结合。钙调蛋白的抑制作用受10⁻⁶ M左右Ca²⁺浓度变化的调节,并被钙调蛋白抑制剂三氟拉嗪所消除。