Iancu Cristina V, Wright Elizabeth R, Benjamin Jordan, Tivol William F, Dias D Prabha, Murphy Gavin E, Morrison Robert C, Heymann J Bernard, Jensen Grant J
Division of Biology, California Institute of Technology, 1200 E. California Blvd., Pasadena, CA 91125, USA.
J Struct Biol. 2005 Sep;151(3):288-97. doi: 10.1016/j.jsb.2005.07.004.
Electron cryotomography can be used to solve the three-dimensional structures of individual large macromolecules, assemblies, and even small intact cells to medium (approximately 4-8 nm) resolution in a near-native state, but restrictions in the range of accessible views are a major limitation. Here we report on the design, characterization, and demonstration of a new "flip-flop" rotation stage that allows facile and routine collection of two orthogonal tilt-series of cryosamples. Single- and dual-axis tomograms of a variety of samples are compared to illustrate qualitatively the improvement produced by inclusion of the second tilt-series. Exact quantitative expressions are derived for the volume of the remaining "missing pyramid" in reciprocal space. When orthogonal tilt-series are recorded to +/-65 degrees in each direction, as this new cryostage permits, only 11% of reciprocal space is left unmeasured. The tomograms suggest that further improvement could be realized, however, through better software to align and merge dual-axis tilt-series of cryosamples.
电子冷冻断层扫描可用于在接近天然状态下将单个大型大分子、组装体甚至小型完整细胞的三维结构解析到中等(约4-8纳米)分辨率,但可获取视图范围的限制是一个主要局限。在此,我们报告一种新型“翻转”旋转台的设计、表征及演示,该旋转台可方便且常规地采集冷冻样品的两个正交倾斜系列。比较了各种样品的单轴和双轴断层扫描图,以定性说明包含第二个倾斜系列所带来的改进。推导了倒易空间中剩余“缺失棱锥”体积的精确定量表达式。当如这种新型冷冻台所允许的那样在每个方向上记录到+/-65度的正交倾斜系列时,倒易空间中仅11%未被测量。然而,断层扫描图表明,通过更好的软件来对齐和合并冷冻样品的双轴倾斜系列,可实现进一步改进。