Steven A C, Hainfeld J F, Trus B L, Steinert P M, Wall J S
Proc Natl Acad Sci U S A. 1984 Oct;81(20):6363-7. doi: 10.1073/pnas.81.20.6363.
A procedure has been developed for direct determination of radial distributions of density in filamentous and spheroidal particles by analyzing dark-field scanning transmission electron micrographs of unstained freeze-dried specimens. Unlike electron microscopic methods based on staining or shadowing with heavy atoms, this approach can be used to probe the internal structure of macromolecular complexes. As an experimental proving ground, we have applied the procedure to tobacco mosaic virus (TMV) and to RNA-free helical polymers of TMV coat protein. Both structures are found to project outermost diameters of 17.6 +/- 0.4 nm, to have empty axial holes approximately equal to 3.5 nm in diameter, and to have density peaks at radii of 2.5 +/- 0.5 and 6.7 +/- 0.3 nm. Thus visualized, the only significant difference between them is the presence in the virion of an additional density peak at 4.1 +/- 0.5 nm contributed by its internalized RNA molecule. We have also used the procedure to monitor the structural expression of radiation damage in the low electron dose regime prior to the onset of significant mass loss. Changes in the radial density profiles are detected at average doses as low as approximately equal to 400 electrons per nm2: the trend is for the internal structure of these particles to fuse toward a state of uniform density, although the values of their outermost diameters remain unaffected.
通过分析未染色的冷冻干燥标本的暗场扫描透射电子显微照片,已开发出一种直接测定丝状和球状颗粒密度径向分布的方法。与基于用重原子染色或投影的电子显微镜方法不同,这种方法可用于探测大分子复合物的内部结构。作为一个实验验证平台,我们已将该方法应用于烟草花叶病毒(TMV)以及TMV外壳蛋白的无RNA螺旋聚合物。发现这两种结构的最外径均为17.6±0.4 nm,有直径约为3.5 nm的空轴孔,并且在半径为2.5±0.5和6.7±0.3 nm处有密度峰。如此观察到的是,它们之间唯一显著的差异是病毒粒子中由其内化的RNA分子贡献的在4.1±0.5 nm处的一个额外密度峰的存在。我们还使用该方法监测在显著质量损失开始之前低电子剂量范围内辐射损伤的结构表现。在低至约每nm² 400个电子的平均剂量下检测到径向密度分布的变化:趋势是这些颗粒的内部结构向均匀密度状态融合,尽管它们的最外径值不受影响。