Peraldi-Roux S, Mangeat P, Rouot B, Oliver J, Herbute S, Brabet P, Homburger V, Toutant M, Bockaert J, Gabrion J
Laboratoire de Neurobiologie endocrinologique, U.R.A. n 1197, C.N.R.S., Université de Montpellier-II.
C R Acad Sci III. 1991;312(4):157-64.
Monoclonal antibodies have been obtained against a purified fraction of brain G proteins containing the Gi alpha, G0 alpha, G beta, and G gamma subunits. After characterization, two monoclonal antibodies have been used to detect the cellular distribution of the two epitopes in neural, retinal and muscular tissues: ELISA, cross-dot and Western blot demonstrated that F.IV.5 is an anti-G beta antibody specific for the 36 kDa beta-subunit. ELISA, cross-dot and immunocytochemical distribution of the epitopes recognized by F.VII.9 suggested that this antibody recognizes epitopes which are also detected with polyclonal anti-G0 alpha antibodies. With both monoclonal antibodies, we confirmed that G proteins demonstrated a sub-membranous distribution as well as extensively cytoplasmic, axoplasmic or sarcoplasmic distributions in different cell types.
已经获得了针对脑G蛋白纯化组分的单克隆抗体,该组分包含Giα、G0α、Gβ和Gγ亚基。经过表征后,两种单克隆抗体被用于检测这两个表位在神经、视网膜和肌肉组织中的细胞分布:酶联免疫吸附测定(ELISA)、交叉点杂交和蛋白质印迹法表明,F.IV.5是一种针对36 kDaβ亚基的抗Gβ抗体。ELISA、交叉点杂交以及F.VII.9识别的表位的免疫细胞化学分布表明,该抗体识别的表位也能用多克隆抗G0α抗体检测到。使用这两种单克隆抗体,我们证实G蛋白在不同细胞类型中呈现出膜下分布以及广泛的细胞质、轴质或肌浆分布。