{"title":"Protocol for measuring the caspase-8 activity at the DED filaments in adherent cells.","authors":"Corinna König, Inna N Lavrik","doi":"10.1016/j.xpro.2025.104131","DOIUrl":null,"url":null,"abstract":"<p><p>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.<sup>1</sup>.</p>","PeriodicalId":34214,"journal":{"name":"STAR Protocols","volume":"6 4","pages":"104131"},"PeriodicalIF":1.3000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"STAR Protocols","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.xpro.2025.104131","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
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.
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。