Three-dimensional live microscopy beyond the diffraction limit
Creators
- 1. Howard Hughes Medical Institute, Janelia Farm Research Campus, Ashburn, VA 20147 (United States)
Description
In fluorescence microscopy it has become possible to fundamentally overcome the diffraction limited resolution in all three spatial dimensions. However, to have the most impact in biological sciences, new optical microscopy techniques need to be compatible with live cell imaging: image acquisition has to be fast enough to capture cellular dynamics at the new resolution limit while light exposure needs to be minimized to prevent photo-toxic effects. With increasing spatial resolution, these requirements become more difficult to meet, even more so when volumetric imaging is performed. In this review, techniques that have been successfully applied to three-dimensional, super-resolution live microscopy are presented and their relative strengths and weaknesses are discussed. (special issue article)
Availability note (English)
Available from http://dx.doi.org/10.1088/2040-8978/15/9/094002Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Optics (Online)
- Journal Volume
- 15
- Journal Issue
- 9
- Journal Page Range
- [8 p.]
- ISSN
- 2040-8986
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46002124
- Subject category
- S71: CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSICS;
- Descriptors DEI
- DIFFRACTION; FLUORESCENCE; IMAGES; OPTICAL MICROSCOPY; OPTICS; REVIEWS; SPATIAL RESOLUTION; THREE-DIMENSIONAL CALCULATIONS; VISIBLE RADIATION
- Descriptors DEC
- COHERENT SCATTERING; DOCUMENT TYPES; ELECTROMAGNETIC RADIATION; EMISSION; LUMINESCENCE; MICROSCOPY; PHOTON EMISSION; RADIATIONS; RESOLUTION; SCATTERING