Nakanishi H, Obaishi H, Satoh A, Wada M, Mandai K, Satoh K, Nishioka H, Matsuura Y, Mizoguchi A, Takai Y
Takai Biotimer Project, ERATO, Japan Science and Technology Corporation, c/o JCR Pharmaceuticals Co., Ltd., Nishi-ku, Kobe 651-22, Japan.
J Cell Biol. 1997 Nov 17;139(4):951-61. doi: 10.1083/jcb.139.4.951.
We purified from rat brain a novel actin filament (F-actin)-binding protein of approximately 180 kD (p180), which was specifically expressed in neural tissue. We named p180 neurabin (neural tissue-specific F-actin- binding protein). We moreover cloned the cDNA of neurabin from a rat brain cDNA library and characterized native and recombinant proteins. Neurabin was a protein of 1,095 amino acids with a calculated molecular mass of 122,729. Neurabin had one F-actin-binding domain at the NH2-terminal region, one PSD-95, DlgA, ZO-1-like domain at the middle region, a domain known to interact with transmembrane proteins, and domains predicted to form coiled-coil structures at the COOH-terminal region. Neurabin bound along the sides of F-actin and showed F-actin-cross-linking activity. Immunofluorescence microscopic analysis revealed that neurabin was highly concentrated in the synapse of the developed neurons. Neurabin was also concentrated in the lamellipodia of the growth cone during the development of neurons. Moreover, a study on suppression of endogenous neurabin in primary cultured rat hippocampal neurons by treatment with an antisense oligonucleotide showed that neurabin was involved in the neurite formation. Neurabin is a candidate for key molecules in the synapse formation and function.
我们从大鼠脑中纯化出一种分子量约为180 kD的新型肌动蛋白丝(F-肌动蛋白)结合蛋白(p180),该蛋白在神经组织中特异性表达。我们将p180命名为神经结合蛋白(神经组织特异性F-肌动蛋白结合蛋白)。此外,我们从大鼠脑cDNA文库中克隆了神经结合蛋白的cDNA,并对天然蛋白和重组蛋白进行了表征。神经结合蛋白是一种含有1095个氨基酸的蛋白质,计算分子量为122,729。神经结合蛋白在NH2末端区域有一个F-肌动蛋白结合结构域,在中间区域有一个PSD-95、DlgA、ZO、ZO-1样结构域,该结构域已知可与跨膜蛋白相互作用,在COOH末端区域有预测形成卷曲螺旋结构的结构域。神经结合蛋白沿F-肌动蛋白的侧面结合,并表现出F-肌动蛋白交联活性。免疫荧光显微镜分析显示,神经结合蛋白高度集中在成熟神经元的突触中。在神经元发育过程中,神经结合蛋白也集中在生长锥的片状伪足中。此外,一项用反义寡核苷酸处理原代培养的大鼠海马神经元以抑制内源性神经结合蛋白的研究表明,神经结合蛋白参与了神经突的形成。神经结合蛋白是突触形成和功能关键分子的候选者。