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Highly Multiplexed, Super-resolution Imaging of T Cells Using madSTORM
Published on: June 24, 2017
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easySTORM: a robust, lower-cost approach to localisation and TIRF microscopy
Kwasi Kwakwa1, Alexander Savell2,3, Timothy Davies4
1Photonics Group, Physics Department, Imperial College London, London, SW7 2AZ. k.kwakwa@imperial.ac.uk.
Journal of Biophotonics
|September 6, 2016
Summary
We developed a low-cost method for super-resolution microscopy using readily available optical fibers and lasers. This approach makes Total Internal Reflection Fluorescence (TIRF) and Stochastic Optical Reconstruction Microscopy (STORM) more accessible for cell imaging.
Area of Science:
- Biophysics
- Optical Microscopy
- Cell Biology
Background:
- Super-resolution microscopy techniques like TIRF and STORM offer high-resolution cellular imaging.
- Current implementations often involve complex and expensive equipment, limiting widespread adoption.
Purpose of the Study:
- To present a simplified and cost-effective method for achieving TIRF and STORM imaging.
- To make advanced fluorescence microscopy techniques more accessible to researchers.
Main Methods:
- Utilized multimode optical fibers and multimode diode lasers for excitation light.
- Integrated open-source software and straightforward sample preparation protocols.
- Employed Vectashield for non-TIRF imaging applications.
Main Results:
- Successfully implemented a low-cost setup for TIRF and STORM microscopy.
- Demonstrated the capability to image cells labeled with appropriate dyes or fluorescent proteins.
- The developed approach significantly reduces the complexity and cost associated with these imaging modalities.
Conclusions:
- This straightforward, low-cost approach democratizes access to TIRF and STORM super-resolution microscopy.
- Enables researchers to perform advanced cell imaging without significant financial or technical barriers.
- Facilitates wider application of super-resolution techniques in cell biology research.

