Two-dimensional electro-optical multiphoton microscopy

被引:0
|
作者
Farinella, Deano M. [1 ]
Stanek, Samuel [2 ]
Jayakumar, Harishankar [1 ]
Newman, Zachary L. [1 ]
Gable, Jacob [1 ]
Leger, James [2 ]
Kerlin, Aaron [1 ]
机构
[1] Univ Minnesota, Dept Neurosci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Elect & Comp Engn, Minneapolis, MN USA
基金
美国国家卫生研究院;
关键词
multiphoton microscopy; electro-optical deflector; in vivo imaging; voltage imaging; BEAM DEFLECTION; STED NANOSCOPY; ULTRAFAST; INDICATOR;
D O I
10.1117/1.NPh.11.2.025005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Significance: The development of genetically encoded fluorescent indicators of neural activity with millisecond dynamics has generated demand for ever faster two-photon (2P) imaging systems, but acoustic and mechanical beam scanning technologies are approaching fundamental limits. We demonstrate that potassium tantalate niobate (KTN) electro-optical deflectors (EODs), which are not subject to the same fundamental limits, are capable of ultrafast two-dimensional (2D) 2P imaging in vivo. Aim: To determine if KTN-EODs are suitable for 2P imaging, compatible with 2D scanning, and capable of ultrafast in vivo imaging of genetically encoded indicators with millisecond dynamics. Approach: The performance of a commercially available KTN-EOD was characterized across a range of drive frequencies and laser parameters relevant to in vivo 2P microscopy. A second KTN-EOD was incorporated into a dual-axis scan module, and the system was validated by imaging signals in vivo from ASAP3, a genetically encoded voltage indicator. Results: Optimal KTN-EOD deflection of laser light with a central wavelength of 960 nm was obtained up to the highest average powers and pulse intensities tested (power: 350 mW; pulse duration: 118 fs). Up to 32 resolvable spots per line at a 560 kHz line scan rate could be obtained with single-axis deflection. The complete dual-axis EO 2P microscope was capable of imaging a 13 mu m by 13 mu m field-of-view at over 10 kHz frame rate with similar to 0.5 mu m lateral resolution. We demonstrate in vivo imaging of neurons expressing ASAP3 with high temporal resolution. Conclusions: We demonstrate the suitability of KTN-EODs for ultrafast 2P cellular imaging in vivo, providing a foundation for future high-performance microscopes to incorporate emerging advances in KTN-based scanning technology.
引用
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页数:15
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