Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1953852 | Biophysical Journal | 2014 | 8 Pages |
Abstract
By delivering optical images with spatial resolutions below the diffraction limit, several super-resolution fluorescence microscopy techniques opened new opportunities to study biological structures with details approaching molecular structure sizes. They have now become methods of choice for imaging proteins and their nanoscale dynamic organizations in live cells. In this mini-review, we describe and compare the main far-field super-resolution approaches that allow studying endogenous or overexpressed proteins in live cells.
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Authors
Antoine G. Godin, Brahim Lounis, Laurent Cognet,