Pearl M, Fishkind D, Mooseker M, Keene D, Keller T
J Cell Biol. 1984 Jan;98(1):66-78. doi: 10.1083/jcb.98.1.66.
The terminal web of the intestinal brush border contains a spectrin-like protein, TW 260/240 (Glenney, J. R., Jr., P. Glenney, M. Osborne, and K. Weber, 1982, Cell, 28:843-854.) that interconnects the "rootlet" ends of microvillar filament bundles in the terminal web (Hirokawa, N., R. E. Cheng, and M. Willard, 1983, Cell, 32:953-965; Glenney J. R., P. Glenney, and K. Weber, 1983, J. Cell Biol., 96:1491-1496). We have investigated further the structural properties of TW 260/240 and the interaction of this protein with actin. Salt extraction of TW 260/240 from isolated brush borders results in a loss of terminal web cross-linkers primarily from the apical zone directly beneath the plasma membrane. Morphological studies on purified TW 260/240 using the rotary shadowing technique confirm earlier results that this protein is spectrin-like and is in the tetrameric state in buffers of low ionic strength. However, examination of TW 260/240 tetramers by negative staining revealed a molecule much straighter and more uniform in diameter than rotary-shadowed molecules. At salt concentrations at (150 mM KCl) and above (300 mM KCl) the physiological range, we observed a partial dissociation of tetramers into dimers that occurred at both 0 degree and 37 degrees C. We also observed (in the presence of 75 mM KCl) a concentration-dependent self-association of TW 260/240 into sedimentable aggregates. We have studied the interaction of TW 260/240 with actin using techniques of co-sedimentation, viscometry, and both light and electron microscopy. We observed that TW 260/240 can bind and cross-link actin filaments and that this interaction is salt- and pH-dependent. Under optimum conditions (25-75 mM KCl, at pH 7.0) TW 260/240 cross-linked F-actin into long, large-diameter bundles. The filaments within these bundles were tightly packed but loosely ordered. At higher pH (7.5) such bundles were not observed, although binding and cross-linking were detectable by co-sedimentation and viscometry. At higher salt (greater than 150 mM KCl), the binding of TW 260/240 to actin was inhibited. The presence of skeletal muscle tropomyosin had no significant effect on the salt-dependent binding of TW 260/240 to F-actin.
肠刷状缘的终末网含有一种血影蛋白样蛋白,即TW 260/240(格伦尼,J.R.,Jr.,P.格伦尼,M.奥斯本,和K.韦伯,1982年,《细胞》,28:843 - 854),它在终末网中连接微绒毛丝束的“根丝”末端(广川,N.,R.E.程,和M.威拉德,1983年,《细胞》,32:953 - 965;格伦尼J.R.,P.格伦尼,和K.韦伯,1983年,《细胞生物学杂志》,96:1491 - 1496)。我们进一步研究了TW 260/240的结构特性以及该蛋白与肌动蛋白的相互作用。从分离的刷状缘中用盐提取TW 260/240会导致终末网交联蛋白主要从质膜正下方的顶端区域丢失。使用旋转阴影技术对纯化的TW 260/240进行的形态学研究证实了早期的结果,即该蛋白是血影蛋白样的,并且在低离子强度缓冲液中处于四聚体状态。然而,通过负染色检查TW 260/240四聚体发现,该分子比旋转阴影分子更直且直径更均匀。在生理盐浓度范围(150 mM KCl及以上,300 mM KCl),我们观察到四聚体在0℃和37℃时都会部分解离成二聚体。我们还观察到(在75 mM KCl存在下)TW 260/240会发生浓度依赖性的自组装形成可沉降的聚集体。我们使用共沉降、粘度测定以及光学和电子显微镜技术研究了TW 260/240与肌动蛋白的相互作用。我们观察到TW 260/240可以结合并交联肌动蛋白丝,并且这种相互作用依赖于盐和pH值。在最佳条件下(25 - 75 mM KCl,pH 7.0),TW 260/240将F - 肌动蛋白交联成长的、大直径的丝束。这些丝束中的丝紧密排列但排列松散。在较高pH值(7.5)时,虽然通过共沉降和粘度测定可检测到结合和交联,但未观察到这样的丝束。在较高盐浓度(大于150 mM KCl)下,TW 260/240与肌动蛋白的结合受到抑制。骨骼肌原肌球蛋白的存在对TW 260/240与F - 肌动蛋白的盐依赖性结合没有显著影响。