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Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
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Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
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Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
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Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells
Journal Article

Optimization of Experimental Variables Influencing Apoptosome Biosensor in HEK293T Cells

2020
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Overview
The apoptotic protease-activating factor 1 (Apaf-1) split luciferase biosensor has been used as a biological tool for the detection of early stage of apoptosis. The effect of doxorubicin in a cell-based assay and the addition of cytochrome c and ATP in a cell-free system have been used to test the functionality of the reporter for the detection of apoptosome formation. Here, our data established a drug- and cytochrome c/ATP-independent way of apoptosis induction relying on the expression of the biosensor itself to induce formation of apoptosome. Overexpression of Apaf-1 constructs led to increased split luciferase activity and caspase-3 activity in the absence of any drug treatment. Caspase-3 activity was significantly inhibited when caspase-9DN was co-overexpressed, while the activity of the Apaf1 biosensor was significantly increased. Our results show that the Apaf-1 biosensor does not detect etoposide-induced apoptosis.