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多色双光子扫描结构照明显微镜成像活细胞。

Multi-color two-photon scanning structured illumination microscopy imaging of live cells.

机构信息

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.

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.

出版信息

J Biophotonics. 2023 Oct;16(10):e202300077. doi: 10.1002/jbio.202300077. Epub 2023 Jul 6.

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.

摘要

多色双光子显微镜活细胞成像在生物学中至关重要。然而,传统双光子显微镜的有限衍射分辨率限制了其在亚细胞细胞器成像中的应用。最近,我们开发了一种激光扫描双光子非线性结构光照明显微镜(2P-NLSIM),其分辨率提高了三倍。然而,其在低激发功率下对多色活细胞成像的能力尚未得到验证。在这里,为了在低激发功率下提高重建超分辨率图像质量,我们在重建过程中通过将原始图像与参考条纹图案相乘来增加图像调制深度。同时,我们优化了 2P-NLSIM 系统以对活细胞进行成像,包括激发功率、成像速度和视野。所提出的系统可以为活细胞成像提供一种新的工具。

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