Related Experiment Video
Updated: Mar 16, 2026

Super-resolution Imaging of the Bacterial Division Machinery
Published on: January 21, 2013
Reduction of coherent artefacts in super-resolution fluorescence localisation microscopy
Pantelis Georgiades1,2, Viki J Allan2,3, Mark Dickinson3
1Biological Physics, School of Physics and Astronomy, The University of Manchester, Manchester, U.K.
None:
Super-resolution localisation microscopy techniques depend on uniform illumination across the field of view, otherwise the resolution is degraded, resulting in imaging artefacts such as fringes. Lasers are currently the light source of choice for switching fluorophores in PALM/STORM methods due to their high power and narrow bandwidth. However, the high coherence of these sources often creates interference phenomena in the microscopes, with associated fringes/speckle artefacts in the images. We quantitatively demonstrate the use of a polymer membrane speckle scrambler to reduce the effect of the coherence phenomena. The effects of speckle in the illumination plane, at the camera and after software localisation of the fluorophores, were characterised. Speckle phenomena degrade the resolution of the microscope at large length scales in reconstructed images, effects that were suppressed by the speckle scrambler, but the small length scale resolution is unchanged at ∼30 nm.
Related Concept Videos
Super-resolution Fluorescence Microscopy
Confocal Fluorescence Microscopy

