Fluorescence nanoscopy at the sub-10 nm scale

被引:16
|
作者
Masullo, Luciano A. [1 ,2 ]
Szalai, Alan M. [1 ]
Lopez, Lucia F. [2 ]
Stefani, Fernando D. [1 ,2 ]
机构
[1] Consejo Nacl Invest Cient & Tecn CONICET, Ctr Invest Bionanociencias CIBION, Godoy Cruz 2390,C1425FQD, Buenos Aires, Argentina
[2] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Fis, Guiraldes 2620,C1428EHA, Buenos Aires, Argentina
关键词
Super-resolution microscopy; Single-molecule localization; Molecular resolution; SINGLE-MOLECULE LOCALIZATION; INDUCED ENERGY-TRANSFER; SUPERRESOLUTION MICROSCOPY; STED MICROSCOPY; OPTICAL NANOSCOPY; GENERAL-METHOD; RESOLUTION; PROBES; TRACKING; LIGHT;
D O I
10.1007/s12551-021-00864-z
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Fluorescence nanoscopy represented a breakthrough for the life sciences as it delivers 20-30 nm resolution using far-field fluorescence microscopes. This resolution limit is not fundamental but imposed by the limited photostability of fluorophores under ambient conditions. This has motivated the development of a second generation of fluorescence nanoscopy methods that aim to deliver sub-10 nm resolution, reaching the typical size of structural proteins and thus providing true molecular resolution. In this review, we present common fundamental aspects of these nanoscopies, discuss the key experimental factors that are necessary to fully exploit their capabilities, and discuss their current and future challenges.
引用
收藏
页码:1101 / 1112
页数:12
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