Super-resolution and localization fluorescence microscopy techniques have attracted considerable attention in the past decade in particular including the Nobel Prize in Chemistry, 2014.
Academics at King’s College London have developed a novel method based on multiscale temporal filtering to enable high density, artefact free and multi colour localisation microscopy.
Localisation microscopy is a type of super-resolution microscopy that allows images to be taken with resolution better than the diffraction limit. While a popular technique, localisation microscopy suffers from several key limitations. First, the speed is very limited because thousands of frames must be acquired to produce a single super-resolution image. Second, it is fairly frequent for artefacts from the analysis to be present in the image, and detecting and removing these is time consuming and requires some degree of expertise. Third, multicolour images often suffer from chromatic aberration, and correcting this will degrade the resolution.
Previous methods to address these problems have either simply subtracted frames (BALM), or used global correlation information for the whole time series (SOFI, SRRF, 3B). This meant that either the resolution was limited or the reconstruction took a long time to calculate.
Key features
Further advantages with regard to multicolour imaging:
- Allows two colour imaging to be carried out without using an image splitter or double conjugation of fluorophores
- Allows use of more than one fluorophores with similar emission spectra (for example Alexa 647 and Atto 647, two of the highest performance fluorophores)
- Faster compared to other methods such as sequential DNA-PAINT labelling as both colours are imaged simultaneously
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attracted considerable attention
king’s college london
global correlation information
final processing depends
preserves intensity informationwhen