Lens-based fluorescence nanoscopy comprises far-field super-resolution imaging methods that separate nearby features by controlling fluorophore emission states over time. The review frames it as a move beyond diffraction-limited fluorescence microscopy.
First-pass extracted concept
lens-based fluorescence nanoscopy
Aliases
fluorescence nanoscopy, nanoscopy, super-resolution microscopy
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What the tool is doing
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What problem it solves
What it does not solve
Evidence Snippets
The surpassing of this resolution limit in far-field microscopy is currently one of the most momentous developments for studying the living cell, as the move from microscopy to super-resolution microscopy or 'nanoscopy' offers opportunities to study problems in biophysical and biomedical research at a new level of detail.
Supporting Sources
Linked Claims
Similar to conventional far-field microscopy, nanoscopy can be utilized for dynamical, multi-color and three-dimensional imaging of fixed and live cells, tissues or organisms.
Similar to conventional far-field microscopy, nanoscopy can be utilized for dynamical, multi-color and three-dimensional imaging of fixed and live cells, tissues or organisms.
Fluorescence nanoscopy variants can in principle reach molecular spatial resolution.
Each of the variants can in principle reach molecular spatial resolution and has its own advantages and disadvantages.
Existing fluorescence nanoscopy variants separate neighboring features by transiently preparing fluorescent molecules in states of different emission characteristics, usually on and off states that cause adjacent molecules to emit sequentially in time.
All the existing nanoscopy variants separate neighboring features by transiently preparing their fluorescent molecules in states of different emission characteristics in order to make the features discernible. Usually these are fluorescent 'on' and 'off' states causing the adjacent molecules to emit sequentially in time.
Some nanoscopy variants require specific fluorophore transitions and states found only in certain fluorophore subfamilies such as photoswitchable fluorophores, whereas other variants can be realized with standard fluorescent labels.
Some require specific transitions and states that can be found only in certain fluorophore subfamilies, such as photoswitchable fluorophores, while other variants can be realized with standard fluorescent labels.