Wuestehube L J, Luna E J
Department of Biology, Princeton University, New Jersey 08544.
J Cell Biol. 1987 Oct;105(4):1741-51. doi: 10.1083/jcb.105.4.1741.
F-actin affinity chromatography and immunological techniques are used to identify actin-binding proteins in purified Dictyostelium discoideum plasma membranes. A 17-kD integral glycoprotein (gp17) consistently elutes from F-actin columns as the major actin-binding protein under a variety of experimental conditions. The actin-binding activity of gp17 is identical to that of intact plasma membranes: it resists extraction with 0.1 N NaOH, 1 mM dithiothreitol (DTT); it is sensitive to ionic conditions; it is stable over a wide range of pH; and it is eliminated by proteolysis, denaturation with heat, or treatment with DTT and N-ethylmaleimide. gp17 may be responsible for much of the actin-binding activity of plasma membranes since monovalent antibody fragments (Fab) directed primarily against gp17 inhibit actin-membrane binding by 96% in sedimentation assays. In contrast, Fab directed against cell surface determinants inhibit binding by only 0-10%. The actin-binding site of gp17 appears to be located on the cytoplasmic surface of the membrane since Fab against this protein continue to inhibit 96% of actin-membrane binding even after extensive adsorption against cell surfaces. gp17 is abundant in the plasma membrane, constituting 0.4-1.0% of the total membrane protein. A transmembrane orientation of gp17 is suggested since, in addition to the cytoplasmic localization of the actin-binding site, extracellular determinants of gp17 are identified. gp17 is surface-labeled by sulfo-N-hydroxy-succinimido-biotin, a reagent that cannot penetrate the cell membrane. Also, gp17 is glycosylated since it is specifically bound by the lectin, concanavalin A. We propose that gp17 is a major actin-binding protein that is important for connecting the plasma membrane to the underlying microfilament network. Therefore, we have named this protein "ponticulin" from the Latin word, ponticulus, which means small bridge.
利用F-肌动蛋白亲和层析法和免疫学技术来鉴定纯化的盘基网柄菌质膜中的肌动蛋白结合蛋白。在多种实验条件下,一种17-kD的整合糖蛋白(gp17)始终作为主要的肌动蛋白结合蛋白从F-肌动蛋白柱上洗脱下来。gp17的肌动蛋白结合活性与完整质膜的相同:它能抵抗0.1 N NaOH、1 mM二硫苏糖醇(DTT)的提取;对离子条件敏感;在很宽的pH范围内稳定;并且通过蛋白水解、加热变性或用DTT和N-乙基马来酰亚胺处理可将其消除。gp17可能是质膜大部分肌动蛋白结合活性的原因,因为主要针对gp17的单价抗体片段(Fab)在沉降分析中可将肌动蛋白-膜结合抑制96%。相比之下,针对细胞表面决定簇的Fab仅抑制0-10%的结合。gp17的肌动蛋白结合位点似乎位于膜的细胞质表面,因为针对该蛋白的Fab即使在大量吸附细胞表面后仍继续抑制96%的肌动蛋白-膜结合。gp17在质膜中含量丰富,占总膜蛋白的0.4-1.0%。由于除了肌动蛋白结合位点的细胞质定位外,还鉴定出了gp17的细胞外决定簇,因此提示gp17具有跨膜取向。gp17可被磺基-N-羟基琥珀酰亚胺生物素表面标记,这是一种不能穿透细胞膜的试剂。此外,gp17是糖基化的,因为它能被凝集素伴刀豆球蛋白A特异性结合。我们提出gp17是一种主要的肌动蛋白结合蛋白,对于将质膜连接到下面的微丝网络很重要。因此,我们从拉丁词ponticulus(意为小桥)中为这种蛋白命名为“桥粒蛋白”。