期刊文献+

受激辐射损耗超分辨成像技术研究 被引量:6

Super resolution imaging technology of stimulated emission depletion
下载PDF
导出
摘要 受激辐射损耗显微成像(STED)是一种超分辨荧光显微成像技术,它能够突破传统光学衍射极限的限制,把远场光学分辨率提高到百纳米以内,被广泛应用于生物医学等领域,是目前光学显微成像领域研究的热点之一。采用了一种基于超连续谱皮秒脉冲白激光光源的STED显微系统,实现超分辨成像。并从精密合束、脉冲延迟和损耗光残留光强几个方面探讨系统优化,从而获得最佳的成像效果。对直径约25 nm荧光微球成像实验的数据表明:该系统成像分辨率可达约60 nm,分辨能力远远高于衍射极限。另外,系统成功实现了对核孔复合物、微管和微丝等一系列生物样品的超分辨成像,共聚焦成像中某些模糊不清的结构在STED成像中清晰可辨。 Stimulated emission depletion (STED) is a kind of super resolution fluorescence microscopy imaging technology. It can break through the traditional optical diffraction limit, and make the far field optical resolution improved to less than 100 nm, which is widely used in biomedical field, and becomes one of the hotspots in optical imaging research. A STED microscope system based on ultra-continuous spectrum picoseconds pulsed white laser source was introduced, and super-resolution imaging was realized. The optimized results were discussed from the aspects of precise collimation, pulse delay and residual intensity of the STED light, therefore the best imaging effect was obtained. The experiments data of the about 25 nm diameter fluorescent microspheres imaging shows that the resolution of the system is ab9ut 60 nm, which is much higher than the diffraction limit. In addition, the system succeeds in realizing super resolution imaging of nuclear pore complexes, microtubules and microfilaments and a series of biological samples. Some obscure structures imaged in confocal microscopy can be legible in STED imaging.
出处 《红外与激光工程》 EI CSCD 北大核心 2016年第6期123-128,共6页 Infrared and Laser Engineering
基金 国家重大科研装备研制项目(ZDYZ2013-1)
关键词 荧光显微成像 超分辨 受激辐射损耗 fluorescence microscopy imaging super resolution stimulated emission depletion
  • 相关文献

参考文献19

  • 1Hell S W. Far-field optical nanoscopy[J]. Science, 2007, 316 (5828): 1153-1158. 被引量:1
  • 2Liu Y, Ding Y, Alonas E, et al. Achieving hi10 resolution CW STED nanoscopy with a Ti: sapphire oscillator[J]. PIoS One, 2012, 7(6): eAO003. 被引量:1
  • 3Eggeling C, Hell S W. STED Fluorescence Nanoscopy [M]. Betin: Springer, 2014. 被引量:1
  • 4Kuang C, Zhao W, Wang G. Far-field optical nanoscopy based on continuous wave laser stimulated emission depletion [J]. Review of Scientific Instruments, 2010, 81(5): 053709. 被引量:1
  • 5Nelson A J, Gunewardene M S, Hess S T. High speed fluorescence photoactivation localization microscopy imaging [C]//SPIE NanoScience + Engineering. International Society for Optics and Photonics, 2014: 91690P-91690P-7. 被引量:1
  • 6Achurra P, Holden S, Pengo T, et al. Super-Resolution Microscopy Techniques in the Nettroscienees [M]. USA: Humana Press, 2014,: 87-111. 被引量:1
  • 7Klein T, Proppert S, Sauer M. Eight years of single-molecule localization microscopy[J]. Histochemis and Cell Biology, 2014, 141(6): 561-575. 被引量:1
  • 8Kim D, Bujny M, Zhuang X. Structural studies by correlative stochastic optical reconstruction microscopy and electron microscopy[J]. Biophysical Journal, 2014, 106(2): 606a. 被引量:1
  • 9Endesfelder U, Heilemarm M. Advanced Fluorescence Microscopy: Method and Protocols[M]. New York: Springer, 2015: 263-276. 被引量:1
  • 10Tehrani K F, Xu J, Kner P A. Multi-color quantum dot stochastic optical reconstruction microscopy (qSTORM)[C]// SPIE, 2015, 9331: 93310. 被引量:1

二级参考文献1

共引文献9

同被引文献26

引证文献6

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部