Corrigendum to: ‘Live and Large’: Super-Resolution Optical Fluctuation Imaging (SOFI) and Expansion Microscopy (ExM) of Microtubule Remodelling by Rabies Virus P Protein
Ashley M. Rozario, Fabian Zwettler, Sam Duwé, Riley B. Hargreaves, Aaron Brice, Peter Dedecker, Markus Sauer, Gregory W. Moseley, Donna R. Whelan and Toby D. M. Bell
Australian Journal of Chemistry
73(8) 822 - 822
Published: 13 August 2020
Abstract
The field of super-resolution microscopy continues to progress rapidly, both in terms of evolving techniques and methodologies as well as in the development of new multi-disciplinary applications. Two current drivers of innovation are increasing the possible resolution gain and application in live samples. Super-resolution optical fluctuation imaging (SOFI) is well suited to live samples while expansion microscopy (ExM) enables obtainment of sub-diffraction information via conventional imaging. In this Highlight we provide a brief outline of these methods and report results from application of SOFI and ExM in our on-going study into microtubule remodelling by rabies virus P proteins. We show that MT bundles in live cells transfected with rabies virus P3 protein can be visualised using SOFI in a time-lapse fashion for up to half an hour and can be expanded using current Pro-ExM protocols and imaged using conventional microscopy.https://doi.org/10.1071/CH19571_CO
© CSIRO 2020