Finbow M E, Shuttleworth J, Hamilton A E, Pitts J D
Beatson Institute for Cancer Research, Wolfson Laboratory for Molecular Pathology, Glasgow, UK.
EMBO J. 1983;2(9):1479-86. doi: 10.1002/j.1460-2075.1983.tb01611.x.
A new method for the purification of gap junctions is described which depends on the extraction of cell monolayers or tissue homogenates with Triton X-100. The major band on SDS-polyacrylamide gel electrophoresis (PAGE) of junctional preparations from a variety of vertebrate sources has an apparent mol. wt. of 16,000 (16 K). Further evidence for the junctional origin of the 16 K protein is provided by the results of four different experimental approaches. (i) The junctions form a sharp band in potassium iodide density gradients at 1.195 g/cm3 and the 16 K protein is the only detectable band in fractions of this bouyant density. (ii) The junctions are progressively solubilised by increasing concentrations of SDS (in the range 0.1-0.5%) and the dissolution of the junctional structure, observed by electron microscopy, parallels the release of the 16 K protein. (iii) Glutaraldehyde fixation of intact junctions cross-links the 16 K protein. (iv) The recoverable amount of the 16 K protein correlates with known changes in gap junctional area in the regenerating weanling rat liver after partial hepatectomy and in V79 cell cultures exposed to 4beta-phorbol 12-myristate 13-acetate.
本文描述了一种纯化间隙连接的新方法,该方法依赖于用Triton X-100提取细胞单层或组织匀浆。来自多种脊椎动物来源的连接制备物在SDS-聚丙烯酰胺凝胶电泳(PAGE)上的主要条带,其表观分子量为16,000(16K)。四种不同实验方法的结果为16K蛋白的连接起源提供了进一步的证据。(i)间隙连接在碘化钾密度梯度中于1.195 g/cm3处形成一条清晰的条带,16K蛋白是该浮力密度级分中唯一可检测到的条带。(ii)随着SDS浓度增加(在0.1 - 0.5%范围内),间隙连接逐渐溶解,通过电子显微镜观察到的连接结构的溶解与16K蛋白的释放平行。(iii)完整间隙连接的戊二醛固定使16K蛋白交联。(iv)在部分肝切除后的再生幼鼠肝脏以及暴露于4β-佛波醇12-肉豆蔻酸酯13-乙酸酯的V79细胞培养物中,16K蛋白的可回收量与间隙连接面积的已知变化相关。