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Analysis of apoptosis in cell-free systems.

机译:无细胞系统中的细胞凋亡分析。

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Cell-free systems have been instrumental in the identification of several important components of the cell death machinery such as cytochrome c, APAF-1, ICAD/CAD (DFF45/DFF40) and Smac/Diablo. Such systems have also proved invaluable for the detailed analysis of caspase activation mechanisms, caspase activation cascades, proteolysis of caspase substrates, apoptosis-associated chromatin condensation and internucleosomal DNA fragmentation. Here, we describe a cell-free system that we have used routinely in our laboratory for the analysis of caspase activation and associated events. Caspase activation in this system can be triggered either through assembly of the APAF-1 apoptosome by addition of cytochrome c/dATP, or alternatively, by addition of the cytotoxic lymphocyte protease, granzyme B. In both cases, the order of caspase activation events has been established and the relative importance of individual caspases to apoptosis-associated nuclear events, as well as substrate proteolysis, is known. Cell-free systems are therefore very useful for screening potential caspase-inhibitory compounds or other agents that may positively or negatively affect caspase-dependent events in apoptosis.
机译:无细胞系统已在识别细胞死亡机制的几个重要组成部分方面发挥了作用,例如细胞色素c,APAF-1,ICAD / CAD(DFF45 / DFF40)和Smac / Diablo。这种系统对于caspase激活机制,caspase激活级联,caspase底物的蛋白水解,凋亡相关的染色质浓缩和核小体间DNA片段化的详细分析也被证明是无价的。在这里,我们描述了一个无细胞系统,我们在实验室中常规使用该系统来分析caspase激活和相关事件。通过添加细胞色素c / dATP或通过添加细胞毒性淋巴细胞蛋白酶颗粒酶B来组装APAF-1凋亡小体,可以触发该系统中的胱天蛋白酶激活。在这两种情况下,胱天蛋白酶激活事件的顺序已经确定了Caspase对凋亡相关的核事件以及底物蛋白水解的相对重要性。因此,无细胞系统对于筛选潜在的caspase抑制性化合物或其他可能对细胞凋亡中caspase依赖性事件有正面或负面影响的药物非常有用。

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