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同步辐射紫外荧光显微镜揭示细胞和组织中的新探针。

Synchrotron UV fluorescence microscopy uncovers new probes in cells and tissues.

机构信息

Synchrotron SOLEIL, L'Orme des Merisiers, 91192 Gif sur Yvette, France.

出版信息

Microsc Microanal. 2010 Oct;16(5):507-14. doi: 10.1017/S1431927610093852. Epub 2010 Aug 25.

DOI:10.1017/S1431927610093852
PMID:20738889
Abstract

Use of deep ultraviolet (DUV, below 350 nm) fluorescence opens up new possibilities in biology because it does not need external specific probes or labeling but instead allows use of the intrinsic fluorescence that exists for many biomolecules when excited in this wavelength range. Indeed, observation of label free biomolecules or active drugs ensures that the label will not modify the biolocalization or any of its properties. In the past, it has not been easy to accomplish DUV fluorescence imaging due to limited sources and to microscope optics. Two worlds were coexisting: the spectrofluorometric measurements with full spectrum information with DUV excitation, which lacked high-resolution localization, and the microscopic world with very good spatial resolution but poor spectral resolution for which the wavelength range was limited to 350 nm. To combine the advantages of both worlds, we have developed a DUV fluorescence microscope for cell biology coupled to a synchrotron beamline, providing fine tunable excitation from 180 to 600 nm and full spectrum acquired on each point of the image, to study DUV excited fluorescence emitted from nanovolumes directly inside live cells or tissue biopsies.

摘要

深紫外(DUV,低于 350nm)荧光的使用为生物学开辟了新的可能性,因为它不需要外部特定的探针或标记,而是允许利用许多生物分子在这个波长范围内被激发时存在的固有荧光。事实上,对无标记的生物分子或活性药物的观察可以确保标记不会改变其生物定位或任何性质。过去,由于光源和显微镜光学器件的限制,实现 DUV 荧光成像并不容易。两个世界并存:具有 DUV 激发的全光谱信息的光谱荧光测量,缺乏高分辨率定位,以及具有非常好的空间分辨率但光谱分辨率差的显微镜世界,其波长范围限于 350nm。为了结合这两个世界的优势,我们开发了一种用于细胞生物学的 DUV 荧光显微镜,它与同步加速器光束线耦合,提供从 180nm 到 600nm 的可调谐激发,以及在图像的每个点上获取全光谱,以研究从活细胞或组织活检中直接纳米体积内发射的 DUV 激发荧光。

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