Light sheet approaches for improved precision in 3D localization-based super-resolution imaging in mammalian cells [Invited]

被引:39
|
作者
Gustavsson, Anna-Karin [1 ,2 ]
Petrov, Petar N. [1 ]
Moerner, W. E. [1 ,3 ]
机构
[1] Stanford Univ, Dept Chem, 333 Campus Dr, Stanford, CA 94305 USA
[2] Karolinska Inst, Dept Biosci & Nutr, SE-17177 Stockholm, Sweden
[3] Stanford Univ, Biophys Program, 333 Campus Dr, Stanford, CA 94305 USA
来源
OPTICS EXPRESS | 2018年 / 26卷 / 10期
基金
瑞典研究理事会;
关键词
POINT-SPREAD-FUNCTION; PLANE ILLUMINATION MICROSCOPY; SINGLE-MOLECULE LOCALIZATION; SELF-RECONSTRUCTING BEAMS; FIELD-OF-VIEW; FLUORESCENCE MICROSCOPY; STRUCTURED-ILLUMINATION; 3-DIMENSIONAL SUPERRESOLUTION; PARTICLE TRACKING; DIFFRACTION-LIMIT;
D O I
10.1364/OE.26.013122
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The development of imaging techniques beyond the diffraction limit has paved the way for detailed studies of nanostructures and molecular mechanisms in biological systems. Imaging thicker samples, such as mammalian cells and tissue, in all three dimensions, is challenging due to increased background and volumes to image. Light sheet illumination is a method that allows for selective irradiation of the image plane, and its inherent optical sectioning capability allows for imaging of biological samples with reduced background, photobleaching, and photodamage. In this review, we discuss the advantage of combining single-molecule imaging with light sheet illumination. We begin by describing the principles of single-molecule localization microscopy and of light sheet illumination. Finally, we present examples of designs that successfully have married single-molecule super-resolution imaging with light sheet illumination for improved precision in mammalian cells. (c) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:13122 / 13147
页数:26
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