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DOI: 10.3791/62842-v
This article presents an experimental workflow for detecting caspase-8 processing at the death-inducing signaling complex (DISC). The methodology allows for the determination of the composition of the DISC complex, which has broad applications in understanding cell death pathways and apoptosis networks.
Here, an experimental workflow is presented that enables the detection of caspase-8 processing directly at the death-inducing signaling complex (DISC) and determines the composition of this complex. This methodology has broad applications, from unraveling the molecular mechanisms of cell death pathways to the dynamic modeling of apoptosis networks.
Apoptosis initiation is mediated by activation of caspases at marker molecular platforms. We present the detection of the key initiation cell death complex DISC, which serves as a platform for caspase-8 activation. The advantage of this technique is that it allows the detection of the assembly and the composition of the DISC complex along with providing information on caspase-8 processing in this complex.
Begin the experiment with cells that are 80%to 90%confluent and adherent to the dish. Discard the medium and add fresh medium to the adherent cells. Then stimulate the cells with the selected concentration of CD95L by holding the plate at an angle and pipetting the ligand into the medium without touching the adherent cells.
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