
TY  - JOUR
A1  - Rozario, Ashley M. 
A1  - Zwettler, Fabian 
A1  - Duwé, Sam 
A1  - Hargreaves, Riley B. 
A1  - Brice, Aaron 
A1  - Dedecker, Peter 
A1  - Sauer, Markus 
A1  - Moseley, Gregory W. 
A1  - Whelan, Donna R. 
A1  - Bell, Toby D. M. 
T1  - <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
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2020
VL  - 73
IS  - 8
SP  - 822
EP  - 822
KW  - 
UR  - https://doi.org/10.1071/CH19571_CO 
N2  - 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. 
ER  -

