Brier J, Fechheimer M, Swanson J, Taylor D L
J Cell Biol. 1983 Jul;97(1):178-85. doi: 10.1083/jcb.97.1.178.
We have studied the abundance, relative gelation activity, and distribution of the 95,000-dalton actin-binding protein in Dictyostelium discoideum amoebae. The 95,000-dalton protein was a prominent polypeptide as assessed using quantitative densitometry and radioimmunoassay. We estimated that this protein comprised approximately 1.2% of the protein in a soluble extract of amoebae. The molar ratio of the dimeric 95,000-dalton protein to actin in the soluble extract was 1:30. The apparent viscosities of actin mixtures with either the purified 95,000-dalton protein or the soluble extract were measured by falling ball viscometry in an attempt to assess the contribution of the 95,000-dalton protein to gelation of the soluble extract. The gelation of the soluble extract was significantly less than that expected from the contribution of the 95,000-dalton protein alone. Consequently, we questioned the validity of quantitative analyses of the contributions of specific actin-binding proteins to the gelation of cell extracts. The apparent distribution of the 95,000-dalton protein was observed in chemically fixed and extracted cells by immunofluorescence microscopy and compared with the distribution of cytoplasm and organelles visible using light microscopy. The 95,000-dalton protein was dispersed throughout the cytoplasm of fixed cells, was apparently excluded from prominent organelles, and displayed brightest fluorescence in regions of hyaline cytoplasm. These regions of hyaline cytoplasm that exhibited the brightest fluorescence were observed in the cortical region of rounded cells and in pseudopods of polarized cells. Thus, cell shape and polarity may also have influenced the apparent distribution of the 95,000-dalton protein observed by immunofluorescence microscopy. Study of the distribution of fluorescein-labeled ovalbumin injected into living cells supported the interpretation that the thickness of the cell and the distribution of organelles contributed to the apparent distribution of the 95,000-dalton protein observed in fixed cells using immunofluorescence microscopy. We suggest that the 95,000-dalton protein contributes to modulation of the consistency and contractility of the cytoplasm of D. discoideum amoebae, since it could cross-link actin filaments in vitro in a reversible process that was regulated by changes in the concentration of calcium and of protons, and since it was present in large quantity in the cytoplasm of these cells.
我们研究了盘基网柄菌变形虫中95,000道尔顿肌动蛋白结合蛋白的丰度、相对凝胶化活性及分布。通过定量光密度测定法和放射免疫测定法评估,95,000道尔顿的蛋白是一种显著的多肽。我们估计这种蛋白约占变形虫可溶性提取物中蛋白的1.2%。可溶性提取物中95,000道尔顿二聚体蛋白与肌动蛋白的摩尔比为1:30。通过落球粘度测定法测量了肌动蛋白与纯化的95,000道尔顿蛋白或可溶性提取物混合物的表观粘度,以评估95,000道尔顿蛋白对可溶性提取物凝胶化的贡献。可溶性提取物的凝胶化明显低于仅由95,000道尔顿蛋白的贡献所预期的值。因此,我们质疑对特定肌动蛋白结合蛋白对细胞提取物凝胶化贡献进行定量分析的有效性。通过免疫荧光显微镜观察化学固定和提取后的细胞中95,000道尔顿蛋白的表观分布,并与使用光学显微镜可见的细胞质和细胞器分布进行比较。95,000道尔顿的蛋白分散在固定细胞的整个细胞质中,明显被排除在突出的细胞器之外,并且在透明细胞质区域显示出最亮的荧光。在圆形细胞的皮质区域和极化细胞的伪足中观察到这些显示最亮荧光的透明细胞质区域。因此,细胞形状和极性也可能影响了通过免疫荧光显微镜观察到的95,000道尔顿蛋白的表观分布。对注入活细胞的荧光素标记卵清蛋白分布的研究支持了这样的解释,即细胞厚度和细胞器分布导致了在固定细胞中使用免疫荧光显微镜观察到的95,000道尔顿蛋白的表观分布。我们认为95,000道尔顿的蛋白有助于调节盘基网柄菌变形虫细胞质的稠度和收缩性,因为它能够在体外以可逆过程交联肌动蛋白丝,该过程受钙和质子浓度变化的调节,并且因为它大量存在于这些细胞的细胞质中。