Three-dimensional structured illumination microscopy with enhanced axial resolution

被引:25
|
作者
Li, Xuesong [1 ,15 ]
Wu, Yicong [1 ,2 ]
Su, Yijun [1 ,2 ,3 ,4 ,15 ]
Rey-Suarez, Ivan [5 ]
Matthaeus, Claudia [6 ]
Updegrove, Taylor B. B. [7 ]
Wei, Zhuang [8 ]
Zhang, Lixia [2 ]
Sasaki, Hideki [3 ,4 ]
Li, Yue [9 ]
Guo, Min [1 ]
Giannini, John P. P. [1 ]
Vishwasrao, Harshad D. D.
Chen, Jiji [2 ]
Lee, Shih-Jong J. [3 ,4 ]
Shao, Lin [10 ,11 ]
Liu, Huafeng [9 ]
Ramamurthi, Kumaran S. S. [7 ]
Taraska, Justin W. W.
Upadhyaya, Arpita [5 ,12 ]
La Riviere, Patrick [13 ,14 ]
Shroff, Hari [1 ,2 ,14 ,15 ]
机构
[1] Natl Inst Biomed Imaging & Bioengn, Lab High Resolut Opt Imaging, NIH, Bethesda, MD 20892 USA
[2] NIH, Adv Imaging & Microscopy Resource, Bethesda, MD 20892 USA
[3] Leica Microsyst Inc, Deerfield, IL USA
[4] SVision LLC, Bellevue, WA USA
[5] Univ Maryland, Inst Phys Sci & Technol, College Pk, MD USA
[6] NHLBI, Biochem & Biophys Ctr, NIH, Bethesda, MD USA
[7] NCI, Lab Mol Biol, NIH, Bethesda, MD USA
[8] Natl Inst Biomed Imaging & Bioengn, Sect Biophoton, NIH, Bethesda, MD USA
[9] Zhejiang Univ, Coll Opt Sci & Engn, State Key Lab Modern Opt Instrumentat, Hangzhou, Peoples R China
[10] Yale Univ, Dept Neurosci, Sch Med, New Haven, CT USA
[11] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT USA
[12] Univ Maryland, Dept Phys, College Pk, MD USA
[13] Univ Chicago, Dept Radiol, Chicago, IL USA
[14] Marine Biol Lab, Woods Hole, MA USA
[15] Howard Hughes Med Inst HHMI, Janelia Res Campus, Ashburn, VA 20147 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SUBCELLULAR-LOCALIZATION; FLUORESCENCE MICROSCOPY; BACILLUS-SUBTILIS; LIGHT-MICROSCOPY; LIVE CELLS; SUPERRESOLUTION; SPORULATION; PROTEIN; FTSZ; CUE;
D O I
10.1038/s41587-022-01651-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Enhanced axial resolution for 3D SIM is achieved with deep learning or four-beam interference. The axial resolution of three-dimensional structured illumination microscopy (3D SIM) is limited to similar to 300 nm. Here we present two distinct, complementary methods to improve axial resolution in 3D SIM with minimal or no modification to the optical system. We show that placing a mirror directly opposite the sample enables four-beam interference with higher spatial frequency content than 3D SIM illumination, offering near-isotropic imaging with similar to 120-nm lateral and 160-nm axial resolution. We also developed a deep learning method achieving similar to 120-nm isotropic resolution. This method can be combined with denoising to facilitate volumetric imaging spanning dozens of timepoints. We demonstrate the potential of these advances by imaging a variety of cellular samples, delineating the nanoscale distribution of vimentin and microtubule filaments, observing the relative positions of caveolar coat proteins and lysosomal markers and visualizing cytoskeletal dynamics within T cells in the early stages of immune synapse formation.
引用
收藏
页码:1307 / +
页数:31
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