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贴壁细胞的相关 VIS-荧光和软 X 射线冷冻显微断层扫描。

Correlative VIS-fluorescence and soft X-ray cryo-microscopy/tomography of adherent cells.

机构信息

Oxford Particle Imaging Centre, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.

出版信息

J Struct Biol. 2012 Feb;177(2):193-201. doi: 10.1016/j.jsb.2011.12.012. Epub 2011 Dec 24.

Abstract

Soft X-ray cryo-microscopy/tomography of vitreous samples is becoming a valuable tool in structural cell biology. Within the 'water-window' wavelength region (2.34-4.37nm), it provides absorption contrast images with high signal to noise ratio and resolution of a few tens of nanometer. Soft X-rays with wavelengths close to the K-absorption edge of oxygen penetrate biological samples with thicknesses in the micrometer range. Here, we report on the application of a recently established extension of the transmission soft X-ray cryo-microscope (HZB TXM) at the beamline U41-XM of the BESSY II electron storage ring by an in-column epi-fluorescence and reflected light cryo-microscope. We demonstrate the new capability for correlative fluorescence and soft X-ray cryo-microscopy/tomography of this instrument along a typical life science experimental approach - the correlation of a fluorophore-tagged protein (pUL34-GFP of pseudorabies virus, PrV, the nuclear membrane-anchored component of the nuclear egress complex of the Herpesviridae which interacts with viral pUL31) in PrV pUL34-GFP/pUL31 coexpressing mammalian cells, with virus-induced vesicular structures in the nucleus, expanding the nucleoplasmic reticulum. Taken together, our results demonstrate new possibilities to study the role of specific proteins in substructures of adherent cells, especially of the nucleus in toto, accessible to electron microscopy in thinned samples only.

摘要

玻璃样样本的软 X 射线冷冻透射/断层扫描技术正在成为结构细胞生物学中的一种有价值的工具。在“水窗”波长区域(2.34-4.37nm)内,它提供了具有高信噪比和几十纳米分辨率的吸收对比图像。波长接近氧的 K 吸收边的软 X 射线可穿透厚度在微米范围内的生物样品。在这里,我们报告了在 BESSY II 电子储存环的 U41-XM 光束线上最近建立的透射软 X 射线冷冻显微镜(HZB TXM)的扩展应用,该扩展应用采用了柱内荧光和反射光冷冻显微镜。我们证明了这种仪器进行相关荧光和软 X 射线冷冻透射/断层扫描的新能力,这是沿着典型的生命科学实验方法进行的 - 对荧光标记蛋白(伪狂犬病病毒的 pUL34-GFP,疱疹病毒核外出口复合物的核膜锚定成分,与病毒 pUL31 相互作用)的相关性进行研究,在 PrV pUL34-GFP/pUL31 共表达的哺乳动物细胞中,病毒诱导的核内囊泡结构,扩大核质网。总之,我们的结果表明了在贴壁细胞的亚结构(特别是整个细胞核)中研究特定蛋白质的作用的新可能性,这些结构仅在经过减薄的样本中才能通过电子显微镜进行研究。

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