Wong J, Hutchison S B, Liem R K
J Biol Chem. 1984 Sep 10;259(17):10867-74.
A soluble isoelectric variant of the 150,000-dalton neurofilament protein was isolated from bovine brain by treating a partially purified filament preparation with a low-ionic-strength high-pH buffer. The protein (S150) had similar peptide maps to the neurofilament component of the same molecular weight (NF150) and was recognized by a polyclonal antibody made against the NF150 polypeptide. However, only half the anti-NF150 activity could be removed with the S150 protein. In addition, the S150 protein had a higher isoelectric point than the NF150 protein. Phosphate analysis indicated that the S150 protein was considerably lessened in phosphate content, which could account for the higher isoelectric point of the protein. It appears, therefore, that the S150 protein may be a precursor of NF150 or the result of phosphatase activity during the isolation procedure. Assembly studies showed that the S150 protein, unlike the NF150 protein, could not assemble with the 70-kDa neurofilament protein, indicating that the phosphate groups which were removed are important in the association of this protein to the neurofilament. When filaments containing all three triplet neurofilament polypeptides or those composed of the 70- and 150-kDa neurofilament proteins were subjected to acid phosphatase, a soluble fraction was obtained, which contained isoelectric variants with higher pI values than the NF150 polypeptide. Only unmodified NF150 protein was found in the insoluble fraction. These results support the argument that removal of phosphate groups results in the dissociation of this protein from the filament.
通过用低离子强度的高pH缓冲液处理部分纯化的细丝制剂,从牛脑中分离出一种150,000道尔顿神经丝蛋白的可溶性等电变体。该蛋白(S150)具有与相同分子量的神经丝成分(NF150)相似的肽图,并且被针对NF150多肽制备的多克隆抗体识别。然而,用S150蛋白只能去除一半的抗NF150活性。此外,S150蛋白的等电点高于NF150蛋白。磷酸盐分析表明,S150蛋白的磷酸盐含量大大降低,这可以解释该蛋白较高的等电点。因此,似乎S150蛋白可能是NF150的前体或分离过程中磷酸酶活性的结果。组装研究表明,与NF150蛋白不同,S150蛋白不能与70-kDa神经丝蛋白组装,这表明被去除的磷酸基团在该蛋白与神经丝的结合中很重要。当含有所有三种三联体神经丝多肽的细丝或由70-和150-kDa神经丝蛋白组成的细丝用酸性磷酸酶处理时,得到一个可溶性部分,其包含等电变体,其pI值高于NF150多肽。在不溶性部分中仅发现未修饰的NF150蛋白。这些结果支持了磷酸基团的去除导致该蛋白从细丝上解离的观点。