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全细胞3D随机光学重建显微镜以纳米级分辨率揭示细胞结构之间的相互作用。

Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution.

作者信息

Huang Bo, Jones Sara A, Brandenburg Boerries, Zhuang Xiaowei

机构信息

Howard Hughes Medical Institute, Harvard University, 12 Oxford St. Cambridge, Massachusetts 02138, USA.

出版信息

Nat Methods. 2008 Dec;5(12):1047-52. doi: 10.1038/nmeth.1274. Epub 2008 Nov 23.

Abstract

The ability to directly visualize nanoscopic cellular structures and their spatial relationship in all three dimensions will greatly enhance our understanding of molecular processes in cells. Here we demonstrated multicolor three-dimensional (3D) stochastic optical reconstruction microscopy (STORM) as a tool to quantitatively probe cellular structures and their interactions. To facilitate STORM imaging, we generated photoswitchable probes in several distinct colors by covalently linking a photoswitchable cyanine reporter and an activator molecule to assist bioconjugation. We performed 3D localization in conjunction with focal plane scanning and correction for refractive index mismatch to obtain whole-cell images with a spatial resolution of 20-30 nm and 60-70 nm in the lateral and axial dimensions, respectively. Using this approach, we imaged the entire mitochondrial network in fixed monkey kidney BS-C-1 cells, and studied the spatial relationship between mitochondria and microtubules. The 3D STORM images resolved mitochondrial morphologies as well as mitochondria-microtubule contacts that were obscured in conventional fluorescence images.

摘要

直接可视化纳米级细胞结构及其三维空间关系的能力将极大地增进我们对细胞内分子过程的理解。在此,我们展示了多色三维(3D)随机光学重建显微镜(STORM)作为定量探测细胞结构及其相互作用的工具。为便于进行STORM成像,我们通过将可光开关的花菁报告分子与激活分子共价连接以辅助生物共轭,生成了几种不同颜色的可光开关探针。我们结合焦平面扫描和折射率失配校正进行3D定位,以获得横向和轴向空间分辨率分别为20 - 30 nm和60 - 70 nm的全细胞图像。使用这种方法,我们对固定的猴肾BS - C - 1细胞中的整个线粒体网络进行了成像,并研究了线粒体与微管之间的空间关系。3D STORM图像解析了线粒体形态以及传统荧光图像中模糊不清的线粒体 - 微管接触。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cb2/2596623/0ab52cfa613e/nihms76581f1.jpg

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