Enabling technologies in super-resolution fluorescence microscopy: reporters, labeling, and methods of measurement

被引:19
作者
Achimovich, Alecia Marie [1 ]
Ai, Huiwang [1 ,2 ]
Gahlmann, Andreas [1 ,2 ]
机构
[1] Univ Virginia, Sch Med, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Chem, Charlottesville, VA 22903 USA
基金
美国国家卫生研究院;
关键词
RESOLUTION LIMIT; BACKGROUND-FREE; ENERGY-TRANSFER; CELL BIOLOGY; DNA-PAINT; IN-VIVO; PROTEIN; BIOSENSORS; TRACKING; CONSTRUCTION;
D O I
10.1016/j.sbi.2019.05.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Super-resolution fluorescence microscopy continues to experience a period of extraordinary development. New instrumentation and fluorescent labeling strategies provide access to molecular and cellular processes that occur on length scales ranging from nanometers to millimeters and on time scales ranging from milliseconds to hours. At the shortest length scales, single-molecule imaging methods now allow measurement of nanoscale localization, motion, and binding kinetics of individual biomolecules. At cellular and intercellular length scales, super-resolution microscopy allows structural and functional imaging of individual cells in tissues and even in whole animals. Here, we review recent advances that have enabled entirely new types of experiments and greatly potentiated existing technologies.
引用
收藏
页码:224 / 232
页数:9
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