Wave front engineering for microscopy of living cells

被引:58
作者
Emiliani, V [1 ]
Cojoc, D
Ferrari, E
Garbin, V
Durieux, C
Coppey-Moisan, M
Di Fabrizio, E
机构
[1] Univ Paris 06, Inst Jacques Monod, UMR 7592, CNRS, F-75251 Paris 05, France
[2] Univ Paris 07, Inst Jacques Monod, UMR 7592, CNRS, F-75251 Paris 05, France
[3] Elettra Sincrotrone, INFM TASC, Nazl Tecnol Avanzate & NanoSCi, LILIT Beamline, I-34012 Trieste, Italy
来源
OPTICS EXPRESS | 2005年 / 13卷 / 05期
关键词
D O I
10.1364/OPEX.13.001395
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
A new method to perform simultaneously three dimensional optical sectioning and optical manipulation is presented. The system combines a multi trap optical tweezers with a video microscope to enable axial scanning of living cells while maintaining the trapping configuration at a fixed position. This is achieved compensating the axial movement of the objective by shaping the wave front of the trapping beam with properly diffractive optical elements displayed on a computer controlled spatial light modulator. Our method has been validated in three different experimental configurations. In the first, we decouple the position of a trapping plane from the axial movements of the objective and perform optical sectioning of a circle of beads kept on a fixed plane. In a second experiment, we extend the method to living cell microscopy by showing that mechanical constraints can be applied on the dorsal surface of a cell whilst performing its fluorescence optical sectioning. In the third experiment, we trapped beads in a three dimensional geometry and perform, always through the same objective, an axial scan of the volume delimited by the beads. (C) 2005 Optical Society of America.
引用
收藏
页码:1395 / 1405
页数:11
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