Saubermann A J, Beeuwkes R, Peters P D
J Cell Biol. 1981 Feb;88(2):268-73. doi: 10.1083/jcb.88.2.268.
New specimen handling and analytic techniques for the application of x-ray microanalysis to studies of cell and organ biology have been recently described (Saubermann et al., 1981, J. Cell Biol. 88:257-267). Based on these techniques, absolute quantitative standardization has been established through x-ray analysis of frozen-hydrated and then dried sections of independently measured standard solutions of elements. These experiments demonstrate that the specific techniques employed have a probable error of less than 10%. Artificial electrolyte gradients established in gelatin were subjected to analysis to determine whether there was elemental displacement under non-membrane-limited conditions at the temperatures employed for sectioning (-30 degrees to -40 degrees C). No significant difference was observed between such gradients in serial sections cut at -30 degrees and -80 degrees C. Similarly, no additional ice-crystal-damage artifact was found in sections cut at -30 degrees C when compared with sections cut at -80 degrees C. Thus, in terms of ice-crystal size, gradient maintenance, and compartmental differentiation, cryosectioning at -30 degrees to -40 degrees C was not associated with redistribution incompatible with 1- to 2-micrometers spatial resolution, and absolute measurements of elemental concentration were practical within regions of this size.
最近已经描述了用于将X射线微分析应用于细胞和器官生物学研究的新标本处理和分析技术(绍伯曼等人,1981年,《细胞生物学杂志》88:257 - 267)。基于这些技术,通过对独立测量的元素标准溶液的冷冻水合然后干燥切片进行X射线分析,建立了绝对定量标准化。这些实验表明,所采用的特定技术的可能误差小于10%。对明胶中建立的人工电解质梯度进行分析,以确定在切片温度(-30摄氏度至-40摄氏度)下非膜限制条件下是否存在元素置换。在-30摄氏度和-80摄氏度下切割的连续切片中的此类梯度之间未观察到显著差异。同样,与在-80摄氏度下切割的切片相比,在-30摄氏度下切割的切片中未发现额外的冰晶损伤伪像。因此,就冰晶大小、梯度维持和区室分化而言,在-30摄氏度至-40摄氏度下进行冷冻切片与不兼容1至2微米空间分辨率的重新分布无关,并且在该大小区域内进行元素浓度的绝对测量是可行的。