Using AIE Luminogen for Longterm and Low-background Three-Photon Microscopic Functional Bioimaging

被引:19
|
作者
Zhu, Zhenfeng [1 ]
Leung, Chris W. T. [2 ]
Zhao, Xinyuan [3 ]
Wang, Yalun [1 ]
Qian, Jun [1 ]
Tang, Ben Zhong [2 ]
He, Sailing [3 ]
机构
[1] Zhejiang Univ, JORCEP Sinoswedish Joint Res Ctr Photon, State Key Lab Modern Opt Instrumentat, Ctr Opt & Electromagnet Res,Zhejiang Prov Key Lab, Hangzhou 310058, Zhejiang, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
[3] Zhejiang Univ, Sch Med, Bioelectromagnet Lab, Hangzhou 310058, Zhejiang, Peoples R China
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
CELL BIOLOGY; FLUORESCENCE; EMISSION; DAMAGE; DOTS;
D O I
10.1038/srep15189
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluorescent probes are one of the most popularly used bioimaging markers to monitor metabolic processes of living cells. However, long-term light excitation always leads to photobleaching of fluorescent probes, unavoidable autofluorescence as well as photodamage of cells. To overcome these limitations, we synthesized a type of photostable luminogen named TPE-TPP with an aggregation induced emission (AIE) characteristic, and achieved its three-photon imaging with femtosecond laser excitation of 1020 nm. By using TPE-TPP as fluorescent probes, three-photon microscopy under 1020 nm excitation showed little photo-damage, as well as low autofluorescence to HeLa cells. Due to the AIE effect, the TPE-TPP nanoaggregates uptaken by cells were resistant to photobleaching under three-photon excitation for an extended period of time. Furthermore, we demonstrated that for the present TPE-TPP AIE the three-photon microscopy (with 1020 nm excitation) had a better signal to noise ratio than the two-photon microscopy (with 810 nm excitation) in tissue imaging.
引用
收藏
页数:9
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