Rogalski A A, Singer S J
J Cell Biol. 1985 Sep;101(3):785-801. doi: 10.1083/jcb.101.3.785.
An integral membrane protein associated with sites of microfilament-membrane attachment has been identified by a newly developed IgG1 monoclonal antibody. This antibody, MAb 30B6, was derived from hybridoma fusion experiments using intact mitotic cells of chick embryo fibroblasts as the immunization vehicle as well as the screening probe for cell surface antigens. In immunofluorescent experiments with fixed cells, MAb 30B6 surface labeling is uniquely correlated with microfilament distributions in the cleavage furrow region of dividing chick embryo fibroblasts and cardiac myocytes in culture. The MAb 30B6 antigen in addition is associated with microfilament-membrane attachment sites in interphase fibroblasts at the dorsal surface, the adhesion plaque region at the ventral surface, and at junction-like regions of cell-cell contact. It is also found co-localized with the membrane-dense plaques of smooth muscle. The MAb 30B6 antigen is expressed in a wide number of chicken cell types (particularly smooth muscle cells, platelets, and endothelial cells), but not in erythrocytes. Some of the molecular characteristics of the MAb 30B6 antigen have been determined from immunoblotting, immunoaffinity chromatography, immunoprecipitation, cell extraction, and charge shift electrophoresis experiments. It is an integral sialoglycoprotein with an apparent molecular mass of 130 kD (reduced form)/107 kD (nonreduced form) in SDS PAGE. Another prominent glycoprotein species with an apparent molecular mass of 175 kD (reduced form)/165 kD (nonreduced form) in SDS PAGE is co-isolated on MAb 30B6 affinity columns, but appears to be antigenically distinct since it is not recognized by MAb 30B6 in immunoblotting or immunoprecipitation experiments. By virtue of its surface distributions relative to actin microfilaments and its integral protein character, we propose that the MAb 30B6 antigen is an excellent candidate for the function of directly or indirectly anchoring microfilaments to the membrane.
一种与微丝-膜附着位点相关的整合膜蛋白已通过新开发的IgG1单克隆抗体得以鉴定。该抗体,即单克隆抗体30B6,源自杂交瘤融合实验,此实验使用鸡胚成纤维细胞的完整有丝分裂细胞作为免疫载体以及细胞表面抗原的筛选探针。在对固定细胞进行的免疫荧光实验中,单克隆抗体30B6的表面标记与培养的分裂鸡胚成纤维细胞和心肌细胞的分裂沟区域中的微丝分布独特相关。此外,单克隆抗体30B6抗原与间期成纤维细胞背表面的微丝-膜附着位点、腹表面的黏着斑区域以及细胞-细胞接触的连接样区域相关。还发现它与平滑肌的膜致密斑共定位。单克隆抗体30B6抗原在多种鸡细胞类型(特别是平滑肌细胞、血小板和内皮细胞)中表达,但在红细胞中不表达。单克隆抗体30B6抗原的一些分子特征已通过免疫印迹、免疫亲和层析、免疫沉淀、细胞提取和电荷转移电泳实验得以确定。它是一种整合唾液糖蛋白,在SDS-PAGE中表观分子量为130 kD(还原形式)/107 kD(非还原形式)。另一种在SDS-PAGE中表观分子量为175 kD(还原形式)/165 kD(非还原形式)的突出糖蛋白在单克隆抗体30B6亲和柱上共分离,但似乎在抗原性上不同,因为在免疫印迹或免疫沉淀实验中它不被单克隆抗体30B6识别。鉴于其相对于肌动蛋白微丝的表面分布及其整合蛋白特性,我们提出单克隆抗体30B6抗原是直接或间接将微丝锚定到膜上功能的极佳候选者。