| Literature DB >> 25418158 |
Antoine G Godin1, Brahim Lounis1, Laurent Cognet2.
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.Mesh:
Year: 2014 PMID: 25418158 PMCID: PMC4213717 DOI: 10.1016/j.bpj.2014.08.028
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033