
%0 Journal Article
%A Rozario, Ashley M. 
%A Zwettler, Fabian 
%A Duwé, Sam 
%A Hargreaves, Riley B. 
%A Brice, Aaron 
%A Dedecker, Peter 
%A Sauer, Markus 
%A Moseley, Gregory W. 
%A Whelan, Donna R. 
%A Bell, Toby D. M. 
%T <i>Corrigendum to</i>: &#x2018;Live and Large&#x2019;: Super-Resolution Optical Fluctuation Imaging (SOFI) and Expansion Microscopy (ExM) of Microtubule Remodelling by Rabies Virus P Protein
%J Australian Journal of Chemistry
%D 2020/08/13
%V 73
%N 8
%P 822-822
%K 
%R https://doi.org/10.1071/CH19571_CO
%U https://www.publish.csiro.au/paper/CH19571_CO 
%X 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. 
