Analysing the Use of Fluorescent Cellular Imaging  and Lentiviral Biosensors for Autophagosome Formation

Microscopy & microtechniques

Analysing the Use of Fluorescent Cellular Imaging  and Lentiviral Biosensors for Autophagosome Formation

12 Mar, 2012

Published over 14 years ago. See the latest and most current information on Microscopy & microtechniques.

Luke Armstrong, Janet Anderl, Karyn Huryn-Selvar, Haizhen Liu, Kevin Su, Mark Santos, Matthew Hsu, Jun Ma,
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In the last 15 years analysis of subcellular structure dynamics has been revolutionised by the refinement of genetically-encoded fusions between fluorescent proteins and cellular structural proteins. By using fluorescence microscopy, such fusion proteins incorporate into the structure of interest without disturbing its function, and permit visualisation of the structure in live cells and in real time [1]. Traditionally, the cDNAs encoding the fusion proteins have been delivered into cells by chemical transfection or electroporation. Such transfection procedures have shortcomings, including variable expression levels and low efficiencies for transfecting primary cells.

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