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用于揭示生物信息的荧光成像及相关技术的发展趋势。

Trends in fluorescence imaging and related techniques to unravel biological information.

作者信息

Haustein Elke, Schwille Petra

机构信息

Biophysics Group, BioTec TU Dresden, Tatzberg 47-51, D-01307 Dresden, Germany.

出版信息

HFSP J. 2007 Sep;1(3):169-80. doi: 10.2976/1.2778852. Epub 2007 Sep 17.

DOI:10.2976/1.2778852
PMID:19404444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2640989/
Abstract

Optical microscopy is among the most powerful tools that the physical sciences have ever provided biology. It is indispensable for basic lab work, as well as for cutting edge research, as the visual monitoring of life processes still belongs to the most compelling evidences for a multitude of biomedical applications. Along with the rapid development of new probes and methods for the analysis of laser induced fluorescence, optical microscopy over past years experienced a vast increase of both new techniques and novel combinations of established methods to study biological processes with unprecedented spatial and temporal precision. On the one hand, major technical advances have significantly improved spatial resolution. On the other hand, life scientists are moving toward three- and even four-dimensional cell biology and biophysics involving time as a crucial coordinate to quantitatively understand living specimen. Monitoring the whole cell or tissue in real time, rather than producing snap-shot-like two-dimensional projections, will enable more physiological and, thus, more clinically relevant experiments, whereas an increase in temporal resolution facilitates monitoring fast nonperiodic processes as well as the quantitative analysis of characteristic dynamics.

摘要

光学显微镜是物理科学为生物学提供的最强大工具之一。它对于基础实验室工作以及前沿研究都是不可或缺的,因为对生命过程的视觉监测仍然是众多生物医学应用中最具说服力的证据之一。随着用于分析激光诱导荧光的新探针和方法的迅速发展,在过去几年中,光学显微镜在新技术以及既定方法的新颖组合方面都有了大幅增长,从而以前所未有的空间和时间精度来研究生物过程。一方面,重大的技术进步显著提高了空间分辨率。另一方面,生命科学家正朝着三维甚至四维细胞生物学和生物物理学发展,将时间作为一个关键坐标来定量理解活体标本。实时监测整个细胞或组织,而不是生成类似快照的二维投影,将能够进行更多生理相关、进而更具临床相关性的实验,而时间分辨率的提高则有助于监测快速的非周期性过程以及对特征动力学进行定量分析。

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本文引用的文献

1
Molecular motors one at a time: FIONA to the rescue.一次一个分子马达:FIONA来帮忙了。
J Phys Condens Matter. 2005 Nov 30;17(47):S3979-95. doi: 10.1088/0953-8984/17/47/023. Epub 2005 Nov 4.
2
Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy.通过受激发射突破衍射分辨率极限:受激发射损耗荧光显微镜技术
Opt Lett. 1994 Jun 1;19(11):780-2. doi: 10.1364/ol.19.000780.
3
Efficient fluorescence inhibition patterns for RESOLFT microscopy.用于RESOLFT显微镜的高效荧光抑制模式。
Opt Express. 2007 Mar 19;15(6):3361-71. doi: 10.1364/oe.15.003361.
4
Electron multiplying CCD based detection for spatially resolved fluorescence correlation spectroscopy.基于电子倍增电荷耦合器件的空间分辨荧光相关光谱检测
Opt Express. 2006 Jun 12;14(12):5013-20. doi: 10.1364/oe.14.005013.
5
Method of obtaining optical sectioning by using structured light in a conventional microscope.在传统显微镜中使用结构光获取光学切片的方法。
Opt Lett. 1997 Dec 15;22(24):1905-7. doi: 10.1364/ol.22.001905.
6
Basic building units and properties of a fluorescence single plane illumination microscope.荧光单平面照明显微镜的基本构建单元及特性
Rev Sci Instrum. 2007 Feb;78(2):023705. doi: 10.1063/1.2428277.
7
Fluorescence correlation spectroscopy: novel variations of an established technique.荧光相关光谱法:一项成熟技术的新变体
Annu Rev Biophys Biomol Struct. 2007;36:151-69. doi: 10.1146/annurev.biophys.36.040306.132612.
8
Ultramicroscopy: three-dimensional visualization of neuronal networks in the whole mouse brain.超微显微镜:全脑小鼠神经网络的三维可视化
Nat Methods. 2007 Apr;4(4):331-6. doi: 10.1038/nmeth1036. Epub 2007 Mar 25.
9
Cdt1 associates dynamically with chromatin throughout G1 and recruits Geminin onto chromatin.在整个G1期,Cdt1与染色质动态结合,并将Geminin招募到染色质上。
EMBO J. 2007 Mar 7;26(5):1303-14. doi: 10.1038/sj.emboj.7601597. Epub 2007 Feb 22.
10
Two-color far-field fluorescence nanoscopy.双色远场荧光纳米显微镜术
Biophys J. 2007 Apr 15;92(8):L67-9. doi: 10.1529/biophysj.107.104497. Epub 2007 Feb 16.