Li Shengwen, Lisanti Michael, Puszkin Saul
Department of Cell Biology, Harvard Medical School, Harvard University, Boston, Massachusetts 02115.
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York.
Bioquim Patol Clin. 1998;62(1):5-17.
NP185, a neuronal-specific protein of 185 kDa, was first discovered when we prepared monoclonal anti-bodies (mAbs) against bovine brain clathrin coated vesicles. Two mAbs, 8G8 and 6G7, permitted us to characterize this protein both biochemically and in development (NP185 is expressed in a NGF-dependent manner in PC12 cells). The expression of NP185 coincides with synaptogenesis. In this work, we have further characterized this protein as follows: Microsequence analysis of immuno-purified native NP185 from bovine brain yielded five peptides that corresponded exactly to the known sequences of murine F1-20 and rat AP180 (renamed AP3); ii) Using an established assay, we show that purified recombinant NP185/AP3 can facilitate clathrin cages assembly; iii) Using deletion mutagenesis, we mapped the epitopes of two distinct mAbs directed against bovine NP185 to a 60 amino acid residue region of the murine recombinant NP185/AP3; iv) Recombinant NP185/AP3 can be phosphorylated by purified casein kinase II in vitro; and v) Recombinant NP185/AP3 directly binds to purified brain tubulin. Since NP185/AP3 binds to tubulin and stimulates the clathrin assembly, it may be involved in the regulation of the transport of clathrin-coated vesicles. Casein kinase II, an enzyme known to be present in clathrin-coated vesicles, may play a role in the regulation of NP185/AP3 for the promotion of clathrin assembly.
NP185是一种185千道尔顿的神经元特异性蛋白,最初是在我们制备针对牛脑网格蛋白包被小泡的单克隆抗体时发现的。两种单克隆抗体8G8和6G7使我们能够从生化和发育方面对这种蛋白进行表征(NP185在PC12细胞中以神经生长因子依赖的方式表达)。NP185的表达与突触形成同时发生。在这项工作中,我们对这种蛋白进行了进一步表征:对从牛脑中免疫纯化的天然NP185进行微序列分析,得到了五个肽段,它们与小鼠F1-20和大鼠AP180(重新命名为AP3)的已知序列完全一致;ii)使用既定的检测方法,我们表明纯化的重组NP185/AP3能够促进网格蛋白笼的组装;iii)使用缺失诱变,我们将针对牛NP185的两种不同单克隆抗体的表位定位到小鼠重组NP185/AP3的一个60个氨基酸残基区域;iv)重组NP185/AP3在体外可被纯化的酪蛋白激酶II磷酸化;v)重组NP185/AP3直接与纯化的脑微管蛋白结合。由于NP185/AP3与微管蛋白结合并刺激网格蛋白组装,则它可能参与网格蛋白包被小泡运输的调节。酪蛋白激酶II是一种已知存在于网格蛋白包被小泡中的酶,可能在调节NP185/AP3以促进网格蛋白组装中发挥作用。