MacMillan L B, Bass M A, Cheng N, Howard E F, Tamura M, Strack S, Wadzinski B E, Colbran R J
Department of Molecular Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0615, USA.
J Biol Chem. 1999 Dec 10;274(50):35845-54. doi: 10.1074/jbc.274.50.35845.
We previously characterized PP1bp134 and PP1bp175, two neuronal proteins that bind the protein phosphatase 1 catalytic subunit (PP1). Here we purify from rat brain actin-cytoskeletal extracts PP1(A) holoenzymes selectively enriched in PP1gamma(1) over PP1beta isoforms and also containing PP1bp134 and PP1bp175. PP1bp134 and PP1bp175 were identified as the synapse-localized F-actin-binding proteins spinophilin (Allen, P. B., Ouimet, C. C., and Greengard, P. (1997) Proc. Natl. Acad. Sci. U. S. A. 94, 9956-9561; Satoh, A., Nakanishi, H., Obaishi, H., Wada, M., Takahashi, K., Satoh, K., Hirao, K., Nishioka, H., Hata, Y., Mizoguchi, A., and Takai, Y. (1998) J. Biol. Chem. 273, 3470-3475) and neurabin (Nakanishi, H., Obaishi, H., Satoh, A., Wada, M., Mandai, K., Satoh, K., Nishioka, H. , Matsuura, Y., Mizoguchi, A., and Takai, Y. (1997) J. Cell Biol. 139, 951-961), respectively. Recombinant spinophilin and neurabin interacted with endogenous PP1 and also with each other when co-expressed in HEK293 cells. Spinophilin residues 427-470, or homologous neurabin residues 436-479, were sufficient to bind PP1 in gel overlay assays, and selectively bound PP1gamma(1) from a mixture of brain protein phosphatase catalytic subunits; additional N- and C-terminal sequences were required for potent inhibition of PP1. Immunoprecipitation of spinophilin or neurabin from crude brain extracts selectively coprecipitated PP1gamma(1) over PP1beta. Moreover, immunoprecipitation of PP1gamma(1) from brain extracts efficiently coprecipitated spinophilin and neurabin, whereas PP1beta immunoprecipitation did not. Thus, PP1(A) holoenzymes containing spinophilin and/or neurabin target specific neuronal PP1 isoforms, facilitating efficient regulation of synaptic phosphoproteins.
我们之前鉴定了PP1bp134和PP1bp175这两种与蛋白磷酸酶1催化亚基(PP1)结合的神经元蛋白。在此,我们从大鼠脑肌动蛋白细胞骨架提取物中纯化出PP1(A)全酶,其选择性地富含PP1γ(1)而非PP1β亚型,并且还含有PP1bp134和PP1bp175。PP1bp134和PP1bp175分别被鉴定为定位于突触的F - 肌动蛋白结合蛋白亲嗜素(艾伦,P.B.,奥伊梅特,C.C.,和格林加德,P.(1997年)美国国家科学院院刊94,9956 - 9561;佐藤,A.,中谷,H.,大星,H.,和田,M.,高桥,K.,佐藤,K.,平尾,K.,西冈,H.,羽多,Y.,水野,A.,和高井,Y.(1998年)生物化学杂志273,3470 - 3475)和神经结合蛋白(中谷,H.,大星,H.,佐藤,A.,和田,M.,万代,K.,佐藤,K.,西冈,H.,松浦,Y.,水野,A.,和高井,Y.(1997年)细胞生物学杂志139,951 - 961)。重组亲嗜素和神经结合蛋白与内源性PP1相互作用,并且在HEK293细胞中共表达时也相互作用。在凝胶覆盖试验中,亲嗜素的427 - 470位残基或神经结合蛋白的同源436 - 479位残基足以结合PP1,并且能从脑蛋白磷酸酶催化亚基混合物中选择性地结合PP1γ(1);有效抑制PP1还需要额外的N端和C端序列。从粗脑提取物中免疫沉淀亲嗜素或神经结合蛋白可选择性地共沉淀PP1γ(1)而非PP1β。此外,从脑提取物中免疫沉淀PP1γ(1)能有效地共沉淀亲嗜素和神经结合蛋白,而PP1β免疫沉淀则不能。因此,含有亲嗜素和/或神经结合蛋白的PP1(A)全酶靶向特定的神经元PP1亚型,有助于高效调节突触磷蛋白。