Three Dimensional Fluorescence Imaging Using Multiple Light-Sheet Microscopy

被引:22
|
作者
Mohan, Kavya [1 ]
Purnapatra, Subhajit B. [1 ]
Mondal, Partha Pratim [1 ,2 ]
机构
[1] Indian Inst Sci, Dept Instrumentat & Appl Phys, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Appl Photon Initiat, Bangalore 560012, Karnataka, India
来源
PLOS ONE | 2014年 / 9卷 / 06期
关键词
LIVE CELLS; RESOLUTION; MULTILAYER; DYNAMICS; PROTEIN; BEAM;
D O I
10.1371/journal.pone.0096551
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Employing spatial filter in the excitation arm of a SPIM system, we successfully generated multiple light-sheets. This improves upon the existing SPIM system and is capable of 3D volume imaging by simultaneously illuminating multiple planes in the sample. Theta detection geometry is employed for data acquisition from multiple specimen layers. This detection scheme inherits many advantages including, background reduction, cross-talk free fluorescence detection and high-resolution at long working distance. Using this technique, we generated 5 equi-intense light-sheets of thickness approximately 7: 5 mm with an inter-sheet separation of 15 mm. Moreover, the light-sheets generated by MLSM is found to be 2 times thinner than the state-of-art SPIM system. Imaging of fluorescently coated yeast cells of size 4 +/- 1 mm (encaged in Agarose gel-matrix) is achieved. Proposed imaging technique may accelerate the field of fluorescence microscopy, cell biology and biophotonics.
引用
收藏
页数:8
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