生物x射线微分析的改进:标本制备的冷冻包埋和数据解释的多元统计分析。

Scanning microscopy. Supplement Pub Date : 1994-01-01
C Quintana, N Bonnet
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引用次数: 0

摘要

对于生物x射线微分析,低温包埋(CE)联合低温固定(CF)和低温脱水(CD)已经在1984年由Wróblewski和Wroblewski提出作为冻干冷冻切片的替代方法。冷冻干燥(FD)的CD通常被推荐,因为它可以更好地保留扩散元素。冷冻取代CD法具有操作简单、超微结构保存重现性强、树脂渗透问题少等优点。我们利用自制的CS和CE装置,在新的Lowicryl K11M和HM23树脂中增加了扩散元素的保留。这些树脂允许样品分别保存在213K和193K的最高温度下。应用多元统计分析(MSA)对x射线数据(光谱和图)可以研究不同核区和细胞质中被分析元素之间的相关性。用MSA获得的“阶乘”图像显示了P和K(核酸)之间强相关的区室和S和K(蛋白质)之间强相关的区室。我们建议MSA方法的未来应用将在亚细胞水平上增加对扩散因子的生理病理区隔的了解。
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Improvements in biological X-ray microanalysis: cryoembedding for specimen preparation and multivariate statistical analysis for data interpretation.

For biological X-ray microanalysis, cryoembedding (CE) combined with cryofixation (CF) and cryodehydration (CD) was already proposed as an alternative method to freeze-dried cryosections in 1984 by Wróblewski and Wroblewski. CD by freeze-drying (FD) is usually recommended because it provides better retention of diffusible elements. CD by freeze-substitution (FS) has the advantage of being simpler, giving more reproducible preservation of ultrastructure and causing fewer problems for resin infiltration. We have increased the retention of diffusible elements by using home-made devices for CS and CE in the new Lowicryl K11M and HM23 resins. These resins allow samples to be kept at a maximum temperature of 213K and 193K respectively. Application of multivariate statistical analysis (MSA) to X-ray data (spectra and maps) allows the study of correlations between the analyzed elements in different nuclear areas and in the cytoplasm. The "factorial" images, obtained with MSA, display the compartments of strong correlation between P and K (nucleic acids) and the compartments of strong correlation between S and K (proteins). We suggest that the future application of MSA methods will provide increased knowledge of the physio-pathological compartmentation of diffusible elements at the subcellular level.

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Nucleic acid detection by in situ molecular immunogold labeling procedures. Hydration-scanning tunneling microscopy as a reliable method for imaging biological specimens and hydrophilic insulators. Imaging molecular structure of channels and receptors with an atomic force microscope. Atomic force microscopy of DNA, nucleoproteins and cellular complexes: the use of functionalized substrates. Microscopic analysis of DNA and DNA-protein assembly by transmission electron microscopy, scanning tunneling microscopy and scanning force microscopy.
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