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New insights into apoptosome structure and function

机译:新洞察患者结构和功能

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The apoptosome is a platform that activates apical procaspases in response to intrinsic cell death signals. Biochemical and structural studies in the past two decades have extended our understanding of apoptosome composition and structure, while illuminating the requirements for initiator procaspase activation. A number of studies have now provided high-resolution structures for apoptosomes from C. elegans (CED-4), D. melanogaster (Dark), and H. sapiens (Apaf-1), which define critical protein interfaces, including intra and interdomain interactions. This work also reveals interactions of apoptosomes with their respective initiator caspases, CED-3, Dronc and procaspase-9. Structures of the human apoptosome have defined the requirements for cytochrome c binding, which triggers the conversion of inactive Apaf-1 molecules to an extended, assembly competent state. While recent data have provided a detailed understanding of apoptosome formation and procaspase activation, they also highlight important evolutionary differences with functional implications for caspase activation.
机译:Apoptosome是一个平台,用于响应于内在细胞死亡信号而激活顶端倾向酶。在过去二十年中的生化和结构研究延长了我们对凋亡器组合物和结构的理解,同时照亮了引发剂促进酶活化的要求。现在,许多研究现在为来自C.杆状杆菌(CED-4),D. melanogaster(暗)和H. sapiens(APAF-1)的H. sapiens(APAF-1)提供了高分辨率结构,其定义了临界蛋白质界面,包括内部和互联区互动。这项工作还揭示了凋亡与各自的引发剂半酶的相互作用,CED-3,DRONC和Procaspase-9。人体凋亡的结构已经限定了细胞色素C结合的要求,其触发了惰性APAF-1分子转化为延长的大会主管状态。虽然最近的数据已经提供了对凋亡组形成和促进酶活性的详细了解,但它们还突出了具有对Caspase激活的功能影响的重要进化差异。

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