Combination of Structured Illumination Microscopy with Hyperspectral Imaging for Cell Analysis

被引:9
|
作者
Liu, Guoxuan [1 ]
Yang, Huaidong [1 ]
Zhao, Hansen [2 ]
Zhang, Yinxin [3 ]
Zhang, Sichun [2 ]
Zhang, Xinrong [2 ]
Jin, Guofan [1 ]
机构
[1] Tsinghua Univ, Dept Precis Instrument, State Key Lab Precis Measurement Technol & Instru, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing Key Lab Microanalyt Methods & Instrumenta, Beijing 100084, Peoples R China
[3] Tianjin Univ, Key Lab Optoelect Informat Technol, Minist Educ, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
RESOLUTION LIMIT; LIVE CELLS; NANOSCOPY; RECONSTRUCTION; SPECTROMETER;
D O I
10.1021/acs.analchem.1c00660
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Existing structured illumination microscopy (SIM) allows super-resolution live-cell imaging in few color channels that provide merely morphological information but cannot acquire the sample spectrum that is strongly relevant to the underlying physicochemical property. We develop hyperspectral SIM which enables high-speed spectral super-resolution imaging in SIM for the first time. Through optically mapping the three-dimensional (x, y, and.) datacube of the sample to the detector plane, hyperspectral SIM allows snapshot spectral imaging of the SIM raw image, detecting the sample spectrum while retaining the high-speed and super-resolution characteristics of SIM. We demonstrate hyperspectral SIM imaging and reconstruct a datacube containing 31 super-resolution images of different wavelengths from only 9 exposures, achieving a 15 nm spectral resolution. We show time-lapse hyperspectral SIM imaging that achieves an imaging speed of 2.7 s per datacube.31-fold faster than the existing wavelength scanning strategy. To demonstrate the great prospects for further combining hyperspectral SIM with various spectral analysis methods, we also perform spectral unmixing of the hyperspectral SIM result while imaging the spectrally overlapped sample.
引用
收藏
页码:10056 / 10064
页数:9
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