在贴壁细胞的DED细丝上测量caspase-8活性的方案。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Corinna König, Inna N Lavrik
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引用次数: 0

摘要

外源性凋亡的关键阶段是死亡诱导信号复合体(DISC)上procaspase-8的激活,其中procaspase-8组装成死亡效应域(DED)细丝。在这里,我们提出了一种直接在DISC上测量caspase-8活性的方案。我们描述了细胞培养、凋亡诱导、免疫沉淀、caspase-8测定和western blot分析的步骤。这种方法能够分析caspase-8在其天然复合物中的活化,并可用于评估靶向caspase-8的药理学抑制剂的功效。有关本协议使用和执行的完整细节,请参阅König et al.1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol for measuring the caspase-8 activity at the DED filaments in adherent cells.

The key stage of extrinsic apoptosis is the activation of procaspase-8 at the death-inducing signaling complex (DISC), where procaspase-8 assembles into death effector domain (DED) filaments. Here, we present a protocol to measure caspase-8 activity directly at the DISC. We describe steps for cell culture, apoptosis induction, immunoprecipitation, caspase-8 assay, and western blot analysis. This approach enables the analysis of caspase-8 activation in its native complex and can be applied to assess the efficacy of pharmacological inhibitors targeting caspase-8. For complete details on the use and execution of this protocol, please refer to König et al.1.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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