Kaplan M P, Chin S S, Macioce P, Srinawasan J, Hashim G, Liem R K
Department of Pathology, Columbia University College of Physicians and Surgeons, New York, NY 10032.
J Neurosci Res. 1991 Nov;30(3):545-54. doi: 10.1002/jnr.490300312.
Peptides corresponding to sequences from the amino-terminal "head" regions of the low, middle, and high molecular weight neurofilament proteins (NF-L, NF-M, and NF-H) were synthesized by a modification of the Merrifield solid-phase method, and a panel of polyclonal antibodies to these epitopes were prepared in rabbits by the injection of synthetic peptides conjugated to the carrier protein keyhole limpet hemocyanin (KLH). An additional, monoclonal antibody recognizing both glial fibrillary acidic protein (GFAP) and vimentin was also produced, by fusion of cells of the mouse myeloma line NS-1 with spleen cells from a mouse immunized with cytoskeletal extracts. Antibody specificities were confirmed by a combination of Western blotting against cytoskeletal extracts and immunofluorescence using both rat brain sections and fibroblasts transfected with fully encoding cDNAs for each neurofilament protein, driven by viral promoters.
通过对Merrifield固相法进行改进,合成了与低分子量、中分子量和高分子量神经丝蛋白(NF-L、NF-M和NF-H)氨基末端“头部”区域序列相对应的肽段。通过注射与载体蛋白钥孔血蓝蛋白(KLH)偶联的合成肽,在兔体内制备了针对这些表位的一组多克隆抗体。还通过将小鼠骨髓瘤细胞系NS-1的细胞与用细胞骨架提取物免疫的小鼠的脾细胞融合,产生了一种额外的、识别胶质纤维酸性蛋白(GFAP)和波形蛋白的单克隆抗体。通过对细胞骨架提取物进行蛋白质印迹分析以及使用大鼠脑切片和用病毒启动子驱动的每种神经丝蛋白的全长编码cDNA转染的成纤维细胞进行免疫荧光分析,证实了抗体的特异性。