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集成于共聚焦显微镜中的用于生物应用的单光束光镊。

Single beam optical trapping integrated in a confocal microscope for biological applications.

作者信息

Visscher K, Brakenhoff G J

机构信息

Department of Molecular Cell Biology, University of Amsterdam, The Netherlands.

出版信息

Cytometry. 1991;12(6):486-91. doi: 10.1002/cyto.990120604.

DOI:10.1002/cyto.990120604
PMID:1764973
Abstract

Confocal microscopy is very useful in biology because of its three dimensional imaging capacities and has proven to be an excellent tool to study the 3D organization of, for instance, cell structures. This property of confocal microscopy makes it also very suitable for observation during guidance of the three dimensional manipulation of single cells or cell elements. Therefore we decided to integrate a confocal microscope and a single beam optical manipulator into a single instrument. The advantage of optical manipulation over mechanical techniques is that it is non-invasive and therefore may be applied on living (micro-) organisms and cells. The creation of an effective single beam optical trap requires the use of a high numerical aperture (N.A.) objective to focus the laser beam. In this paper we briefly discuss the vertical or axial force exerted on a sphere in a single beam trap. The axial force on a sphere placed on the optical axis, caused by reflection and refraction, is calculated applying a electromagnetic vector diffraction theory to determine the field distribution in the focal region. One of the results is that the particle also experiences a vertical trapping force towards the focusing lens when it is in the strongly convergent part of the field in addition to the known negative signed trapping force in the divergent part of the field. Further we describe an instrumental approach to realize optical trapping in which the optical trap position is controlled by moving the focusing objective only.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

共聚焦显微镜由于其三维成像能力,在生物学领域非常有用,并且已被证明是研究例如细胞结构三维组织的优秀工具。共聚焦显微镜的这一特性使其也非常适合在单细胞或细胞元件的三维操作引导过程中进行观察。因此,我们决定将共聚焦显微镜和单光束光学操纵器集成到一台仪器中。光学操纵相对于机械技术的优势在于它是非侵入性的,因此可应用于活的(微观)生物体和细胞。创建有效的单光束光阱需要使用高数值孔径(N.A.)物镜来聚焦激光束。在本文中,我们简要讨论了单光束阱中施加在球体上的垂直或轴向力。通过应用电磁矢量衍射理论来确定焦区的场分布,计算了放置在光轴上的球体由于反射和折射而产生的轴向力。结果之一是,除了在发散场部分已知的负号捕获力外,当粒子处于场的强会聚部分时,它还会受到朝向聚焦透镜的垂直捕获力。此外,我们描述了一种实现光阱的仪器方法,其中通过仅移动聚焦物镜来控制光阱位置。(摘要截短于250字)

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Single beam optical trapping integrated in a confocal microscope for biological applications.集成于共聚焦显微镜中的用于生物应用的单光束光镊。
Cytometry. 1991;12(6):486-91. doi: 10.1002/cyto.990120604.
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Independent and simultaneous three-dimensional optical trapping and imaging.独立且同步的三维光学捕获与成像
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Force mapping during the formation and maturation of cell adhesion sites with multiple optical tweezers.利用多个光学镊子研究细胞黏附位点形成和成熟过程中的力映射。
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Resource Letter: LBOT-1: Laser-based optical tweezers.资料信函:LBOT - 1:基于激光的光镊
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Physiological monitoring of optically trapped cells: assessing the effects of confinement by 1064-nm laser tweezers using microfluorometry.光镊捕获细胞的生理监测:利用显微荧光测定法评估1064纳米激光镊的限制作用。
Biophys J. 1996 Oct;71(4):2158-67. doi: 10.1016/S0006-3495(96)79417-1.