CHARACTERIZATION OF A PANEL OF NEUROFILAMENT ANTIBODIES RECOGNIZING N-TERMINAL EPITOPES

被引:32
作者
KAPLAN, MP
CHIN, SSM
MACIOCE, P
SRINAWASAN, J
HASHIM, G
LIEM, RKH
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,DEPT PATHOL,630 W 168 ST,NEW YORK,NY 10032
[2] COLUMBIA UNIV COLL PHYS & SURG,DEPT ANAT,NEW YORK,NY 10032
[3] COLUMBIA UNIV COLL PHYS & SURG,DEPT CELL BIOL,NEW YORK,NY 10032
[4] NYU,SCH MED,DEPT PHARMACOL,NEW YORK,NY 10003
[5] ST LUKES ROOSEVELT HOSP,EXPTL IMMUNOL LAB,NEW YORK,NY 10025
[6] IST SUPER SANITA,BIOL CELLULARE LAB,I-00161 ROME,ITALY
关键词
CYTOSKELETON; NEUROFILAMENTS; VIMENTIN; GFAP; ANTIBODIES;
D O I
10.1002/jnr.490300312
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:545 / 554
页数:10
相关论文
共 30 条