Optical traps induce fluorophore photobleaching by two-photon excitation

被引:0
|
作者
Lu, Suoang [1 ]
Chemla, Yann R. [1 ,2 ,3 ]
机构
[1] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[2] Univ Illinois, Ctr Biophys & Quantitat Biol, Urbana, IL 61801 USA
[3] Univ Illinois, Ctr Phys Living Cells, Urbana, IL 61801 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
DNA-MOLECULES; SINGLE; PHOTOSTABILITY; SPECTROSCOPY; DYES;
D O I
10.1016/j.bpj.2023.10.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Techniques combining optical tweezers with fluorescence microscopy have become increasingly popular. Unfor-tunately, the high-power, infrared lasers used to create optical traps can have a deleterious effect on dye stability. Previous studies have shown that dye photobleaching is enhanced by absorption of visible fluorescence excitation plus infrared trap pho-tons, a process that can be significantly reduced by minimizing simultaneous exposure to both light sources. Here, we report another photobleaching pathway that results from direct excitation by the trapping laser alone. Our results show that this trap-induced fluorescence loss is a two-photon absorption process, as demonstrated by a quadratic dependence on the intensity of the trapping laser. We further show that, under conditions typical of many trap-based experiments, fluorescence emission of certain fluorophores near the trap focus can drop by 90% within 1 min. We investigate how photostability is affected by the choice of dye molecule, excitation and emission wavelength, and labeled molecule. Finally, we discuss the different photobleaching pathways in combined trap-fluorescence measurements, which guide the selection of optimal dyes and conditions for more robust experimental protocols.
引用
收藏
页码:4316 / 4325
页数:10
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