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Multi-color two-photon scanning structured illumination microscopy imaging of live cells.
Wang, Meiting; Chen, Jiajie; Wu, Wenshuai; Wang, Lei; Zheng, Xiaomin; Xu, Gaixia; Qu, Junle; Gao, Bruce Zhi; Shao, Yonghong.
Afiliación
  • Wang M; Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering, Shenzhen University, Shenzhen, China.
  • Chen J; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
  • Wu W; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
  • Wang L; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
  • Zheng X; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
  • Xu G; Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering, Shenzhen University, Shenzhen, China.
  • Qu J; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
  • Gao BZ; Department of Bioengineering and COMSET, Clemson University, Clemson, South Carolina, USA.
  • Shao Y; Key Laboratory of Optoelectronic Devices and Systems of the Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
J Biophotonics ; 16(10): e202300077, 2023 10.
Article en En | MEDLINE | ID: mdl-37293715
ABSTRACT
Multi-color two-photon microscopy imaging of live cells is essential in biology. However, the limited diffraction resolution of conventional two-photon microscopy restricts its application to subcellular organelle imaging. Recently, we developed a laser scanning two-photon non-linear structured illumination microscope (2P-NLSIM), whose resolution improved three-fold. However, its ability to image polychromatic live cells under low excitation power has not been verified. Here, to improve the reconstruction super-resolution image quality under low excitation power, we increased the image modulation depth by multiplying the raw images with the reference fringe patterns in the reconstruction process. Simultaneously, we optimized the 2P-NLSIM system to image live cells, including the excitation power, imaging speed, and field of view. The proposed system could provide a new imaging tool for live cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Iluminación / Fotones Idioma: En Revista: J Biophotonics Asunto de la revista: BIOFISICA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Iluminación / Fotones Idioma: En Revista: J Biophotonics Asunto de la revista: BIOFISICA Año: 2023 Tipo del documento: Article País de afiliación: China