Mücke N, Kreplak L, Kirmse R, Wedig T, Herrmann H, Aebi U, Langowski J
Division Biophysics of Macromolecules, German Cancer Research Center, 69120 Heidelberg, Germany.
J Mol Biol. 2004 Jan 30;335(5):1241-50. doi: 10.1016/j.jmb.2003.11.038.
Eukaryotic cells contain three cytoskeletal filament systems that exhibit very distinct assembly properties, supramolecular architectures, dynamic behaviour and mechanical properties. Microtubules and microfilaments are relatively stiff polar structures whose assembly is modulated by the state of hydrolysis of the bound nucleotide. In contrast, intermediate filaments (IFs) are more flexible apolar structures assembled from a approximately 45 nm long coiled-coil dimer as the elementary building block. The differences in flexibility that exist among the three filament systems have been described qualitatively by comparing electron micrographs of negatively stained dehydrated filaments and by directly measuring the persistence length of F-actin filaments (approximately 3-10 microm) and microtubules (approximately 1-8 mm) by various physical methods. However, quantitative data on the persistence length of IFs are still missing. Toward this goal, we have carried out atomic force microscopy (AFM) in physiological buffer to characterise the morphology of individual vimentin IFs adsorbed to different solid supports. In addition, we compared these images with those obtained by transmission electron microscopy (TEM) of negatively stained dehydrated filaments. For each support, we could accurately measure the apparent persistence length of the filaments, yielding values ranging between 0.3 microm and 1 microm. Making simple assumptions concerning the adsorption mechanism, we could estimate the persistence length of an IF in a dilute solution to be approximately 1 microm, indicating that the lower measured values reflect constraints induced by the adsorption process of the filaments on the corresponding support. Based on our knowledge of the structural organisation and mechanical properties of IFs, we reason that the lower persistence length of IFs compared to that of F-actin filaments is caused by the presence of flexible linker regions within the coiled-coil dimer and by postulating the occurrence of axial slipping between dimers within IFs.
真核细胞包含三种细胞骨架丝系统,它们表现出非常不同的组装特性、超分子结构、动态行为和机械性能。微管和微丝是相对较硬的极性结构,其组装受结合核苷酸水解状态的调节。相比之下,中间丝(IFs)是由大约45纳米长的卷曲螺旋二聚体作为基本构建块组装而成的更灵活的非极性结构。通过比较负染色脱水丝的电子显微镜照片以及通过各种物理方法直接测量F-肌动蛋白丝(约3 - 10微米)和微管(约1 - 8毫米)的持续长度,已经定性地描述了三种丝系统之间存在的柔韧性差异。然而,关于中间丝持续长度的定量数据仍然缺失。为了实现这一目标,我们在生理缓冲液中进行了原子力显微镜(AFM)实验,以表征吸附在不同固体支持物上的单个波形蛋白中间丝的形态。此外,我们将这些图像与负染色脱水丝的透射电子显微镜(TEM)图像进行了比较。对于每种支持物,我们可以准确测量丝的表观持续长度,得到的值在0.3微米到1微米之间。基于关于吸附机制的简单假设,我们可以估计在稀溶液中中间丝的持续长度约为1微米,这表明较低的测量值反映了丝在相应支持物上的吸附过程所引起的限制。基于我们对中间丝的结构组织和机械性能的了解,我们推断中间丝与F-肌动蛋白丝相比持续长度较低是由卷曲螺旋二聚体内存在柔性连接区域以及假设中间丝内二聚体之间发生轴向滑动所致。