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单细胞中的相关细胞器荧光显微镜和同步辐射X射线化学元素成像

Correlative organelle fluorescence microscopy and synchrotron X-ray chemical element imaging in single cells.

作者信息

Roudeau Stéphane, Carmona Asuncion, Perrin Laura, Ortega Richard

机构信息

University of Bordeaux, CNRS, CENBG, UMR 5797, 33170, Gradignan, France.

出版信息

Anal Bioanal Chem. 2014 Nov;406(27):6979-91. doi: 10.1007/s00216-014-8004-4. Epub 2014 Jul 15.

Abstract

X-ray chemical element imaging has the potential to enable fundamental breakthroughs in the understanding of biological systems because chemical element interactions with organelles can be studied at the sub-cellular level. What is the distribution of trace metals in cells? Do some elements accumulate within sub-cellular organelles? What are the chemical species of the elements in these organelles? These are some of the fundamental questions that can be addressed by use of X-ray chemical element imaging with synchrotron radiation beams. For precise location of the distribution of the elements, identification of cellular organelles is required; this can be achieved, after appropriate labelling, by use of fluorescence microscopy. As will be discussed, this approach imposes some limitations on sample preparation. For example, standard immunolabelling procedures strongly modify the distribution of the elements in cells as a result of the chemical fixation and permeabilization steps. Organelle location can, however, be performed, by use of a variety of specific fluorescent dyes or fluorescent proteins, on living cells before cryogenic fixation, enabling preservation of element distribution. This article reviews the methods used for fluorescent organelle labelling and X-ray chemical element imaging and speciation of single cells. Selected cases from our work and from other research groups are presented to illustrate the potential of the combination of the two techniques.

摘要

X射线化学元素成像有潜力在理解生物系统方面实现根本性突破,因为可以在亚细胞水平研究化学元素与细胞器的相互作用。细胞中痕量金属的分布是怎样的?某些元素会在亚细胞器内积累吗?这些细胞器中元素的化学形态是什么?这些都是可以通过使用同步辐射束进行X射线化学元素成像来解决的一些基本问题。为了精确确定元素分布的位置,需要识别细胞器;在适当标记后,这可以通过荧光显微镜来实现。正如将要讨论的,这种方法对样品制备有一些限制。例如,由于化学固定和通透步骤,标准免疫标记程序会强烈改变细胞中元素的分布。然而,在低温固定之前,可以使用多种特异性荧光染料或荧光蛋白在活细胞上进行细胞器定位,从而保存元素分布。本文综述了用于荧光细胞器标记以及单细胞的X射线化学元素成像和形态分析的方法。展示了我们的工作以及其他研究小组的一些案例,以说明这两种技术相结合的潜力。

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