Approach to multiparticle parallel tracking in thick samples with three-dimensional nanoresolution

被引:12
作者
Chen, Danni [1 ,2 ,3 ,4 ,5 ]
Yu, Bin [1 ,2 ,3 ,4 ,5 ]
Li, Heng [1 ,2 ,3 ,4 ,5 ]
Huo, Yingdong [1 ,2 ,3 ,4 ,5 ]
Cao, Bo [1 ,2 ,3 ,4 ,5 ]
Xu, Gaixia [1 ,2 ,3 ,4 ,5 ]
Niu, Hanben [1 ,2 ,3 ,4 ,5 ]
机构
[1] Shenzhen Univ, Inst Optoelect, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Key Lab Optoelect Devices & Syst Minist Educ, Shenzhen 518060, Guangdong, Peoples R China
[3] Shenzhen Univ, Shenzhen Key Lab Biomed Engn, Shenzhen 518060, Peoples R China
[4] Shenzhen Univ, Shenzhen Key Lab Biomed Engn, Shenzhen 518060, Peoples R China
[5] Key Lab Micronano Measuring & Imaging Biomed Opt, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
FLUORESCENCE MICROSCOPY; LOCALIZATION ACCURACY; DIFFRACTION-LIMIT; CELLULAR-DYNAMICS; FOCAL PLANES;
D O I
10.1364/OL.38.003712
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
This Letter proposes a method referred to as distorted grating (DG) and double-helix point spread function (DH-PSF) combination microscopy (DDCM), which is capable of multiparticle parallel localization and tracking in a transparent sample thicker than 10 mu m, the thickness of cells. A special phase mask, combining the field depth extension capabilities of DG with the three-dimensional (3D) nanolocalization capabilities of the DH-PSF, is designed for multiparticle parallel localization. Time-lapse tracking of one particle moving along the z axis and parallel tracking of two particles are simulated. Results demonstrate that, with only a single snapshot, particles can be localized, tracking with 3D nanoresolution wherever they are. The theoretical localization precisions of DDCM, DH-PSF, and multifocus microscopy are compared. DDCM results in almost constant localization precisions in all three dimensions for a depth of field larger than 10 mu m. DDCM is expected to become a tool in investigations of important dynamic events in living cells. (C) 2013 Optical Society of America
引用
收藏
页码:3712 / 3715
页数:4
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