X-ray microscopy: preparations for studies of frozen hydrated specimens.

Scanning microscopy. Supplement Pub Date : 1996-01-01
A Osanna, C Jacobsen, A Kalinovsky, J Kirz, J Maser, S Wang
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Abstract

X-ray microscopes provide higher resolution than visible light microscopes. Wet, biological materials with a water thickness of up to about 10 microns can be imaged with good contrast using soft X-rays with wavelengths between the oxygen and carbon absorption edges (at 24 and 43 A). The Stony Brook group has developed and operates a scanning transmission X-ray microscope (STXM) at the National Synchrotron Light Source (NSLS) at Brookhaven National Laboratory. The microscope is used for imaging with a current resolution of 50 nm, and for elemental and chemical state mapping. Radiation damage imposes a significant limitation upon high resolution X-ray microscopy of room temperature wet specimens. Experience from electron microscopy suggests that cryo techniques allow vitrified specimens to be imaged repeatedly. This is due to the increased radiation stability of biological specimens in the frozen hydrated state. Better radiation stability has been shown recently with a cryo transmission X-ray microscope developed by the University of Göttingen, operating at the BESSY storage ring in Berlin, Germany. At Stony Brook, we are developing a cryo scanning transmission X-ray microscope (CryoSTXM) to carry out imaging and spectro-microscopy experiments on frozen hydrated specimens. This article will give an outlook onto the research projects that we plan to perform using the CryoSTXM.

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x射线显微镜:冷冻水合标本研究的准备。
x射线显微镜的分辨率比可见光显微镜高。水厚度约为10微米的湿生物材料可以使用波长在氧和碳吸收边缘(24和43 a)之间的软x射线进行成像,具有良好的对比度。石溪小组在布鲁克海文国家实验室的国家同步加速器光源(NSLS)开发并操作扫描透射x射线显微镜(STXM)。该显微镜用于成像,当前分辨率为50纳米,并用于元素和化学状态映射。辐射损伤对室温湿样的高分辨率x射线显微成像有很大的限制。电子显微镜的经验表明,冷冻技术可以使玻璃化的标本反复成像。这是由于生物标本在冷冻水合状态下的辐射稳定性增加。最近,由Göttingen大学开发的一种低温透射x射线显微镜显示出更好的辐射稳定性,该显微镜在德国柏林的BESSY储存环上运行。在石溪,我们正在开发一种低温扫描透射x射线显微镜(CryoSTXM),用于对冷冻水合标本进行成像和光谱显微镜实验。本文将展望我们计划使用CryoSTXM执行的研究项目。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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