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10.1016/j.abb.2018.01.017

http://scihub22266oqcxt.onion/10.1016/j.abb.2018.01.017
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C5856089!5856089!29410086
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suck abstract from ncbi


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pmid29410086      Arch+Biochem+Biophys 2018 ; 642 (ä): 46-51
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  • Apoptosome formation upon overexpression of native and truncated Apaf-1 in cell-free and cell-based systems #MMPMID29410086
  • Noori AR; Hosseini ES; Nikkhah M; Hosseinkhani S
  • Arch Biochem Biophys 2018[Mar]; 642 (ä): 46-51 PMID29410086show ga
  • Apaf-1 is a cytosolic multi-domain protein in the apoptosis regulatory network. When cytochrome c releases from mitochondria; it binds to WD-40 repeats of Apaf-1 molecule and induces oligomerization of Apaf-1. Here in, a split luciferase assay was used to compare apoptosome formation in cell-free and cell-based systems. This assay uses Apaf-1 tagged with either N-terminal fragment or C-terminal fragment of P. pyralis luciferase. In cell based-system, the apoptosome formation is induced inside the cells which express Apaf-1 tagged with complementary fragments of luciferase while in cell-free system, the apoptosome formation is induced in extracts of the cells. In cell-free system, cytochrome c dependent luciferase activity was observed with full length Apaf-1. However, luciferase activity due to apoptosome formation was much higher in cell based system compared to cell-free system. The truncated Apaf-1 which lacks WD-40 repeats (?Apaf-1) interacted with endogenous Apaf-1 in a different fashion compared to native form as confirmed by different retention time of eluate in gel filtration and binding to affinity column. The interactions between endogenous Apaf-1 and ?Apaf-1 is stronger than its interaction with native exogenous Apaf-1 as indicated by dominant negative effect of ?Apaf-1 on caspase-3 processing.
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