Three-Dimensional Single-Molecule Localization Microscopy in Whole-Cell and Tissue Specimens

被引:26
作者
Liu, Sheng [1 ]
Huh, Hyun [2 ]
Lee, Sang-Hyuk [2 ,3 ]
Huang, Fang [1 ,4 ,5 ]
机构
[1] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[2] Rutgers State Univ, Inst Quantitat Biomed, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Phys & Astron, Piscataway, NJ 08854 USA
[4] Purdue Univ, Purdue Inst Integrat Neurosci, W Lafayette, IN 47907 USA
[5] Purdue Univ, Purdue Inst Inflammat Immunol & Infect Dis, W Lafayette, PA 47907 USA
来源
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 22 | 2020年 / 22卷
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
super-resolution microscopy; fluorescence microscopy; tissue imaging; adaptive optics; light-sheet microscopy; Cramer-Rao lower bound; CRLB; PLANE ILLUMINATION MICROSCOPY; LIGHT-SHEET MICROSCOPY; SAMPLE DRIFT CORRECTION; FIELD-OF-VIEW; FLUORESCENCE MICROSCOPY; ADAPTIVE OPTICS; SUPERRESOLUTION MICROSCOPY; DIFFRACTION-LIMIT; MULTIFOCUS MICROSCOPY; PUPIL FUNCTIONS;
D O I
10.1146/annurev-bioeng-060418-052203
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Super-resolution microscopy techniques are versatile and powerful tools for visualizing organelle structures, interactions, and protein functions in biomedical research. However, whole-cell and tissue specimens challenge the achievable resolution and depth of nanoscopy methods. We focus on three-dimensional single-molecule localization microscopy and review some of the major roadblocks and developing solutions to resolving thick volumes of cells and tissues at the nanoscale in three dimensions. These challenges include background fluorescence, system- and sample-induced aberrations, and information carried by photons, as well as drift correction, volume reconstruction, and photobleaching mitigation. We also highlight examples of innovations that have demonstrated significant breakthroughs in addressing the abovementioned challenges together with their core concepts as well as their trade-offs.
引用
收藏
页码:155 / 184
页数:30
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