首页> 外文OA文献 >Pro-apoptotic proteins released from the mitochondria regulate the protein composition and caspase-processing activity of the native Apaf-1/caspase-9 apoptosome complex.
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Pro-apoptotic proteins released from the mitochondria regulate the protein composition and caspase-processing activity of the native Apaf-1/caspase-9 apoptosome complex.

机译:从线粒体释放的促凋亡蛋白调节天然Apaf-1 / caspase-9凋亡小体复合物的蛋白组成和caspase加工活性。

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摘要

The apoptosome is a large caspase-activating ( approximately 700-1400 kDa) complex, which is assembled from Apaf-1 and caspase-9 when cytochrome c is released during mitochondrial-dependent apoptotic cell death. Apaf-1 the core scaffold protein is approximately 135 kDa and contains CARD (caspase recruitment domain), CED-4, and multiple (13) WD40 repeat domains, which can potentially interact with a variety of unknown regulatory proteins. To identify such proteins we activated THP.1 lysates with dATP/cytochrome c and used sucrose density centrifugation and affinity-based methods to purify the apoptosome for analysis by MALDI-TOF mass spectrometry. First, we used a glutathione S-transferase (GST) fusion protein (GST-casp9(1-130)) containing the CARD domain of caspase-9-(1-130), which binds to the CARD domain of Apaf-1 when it is in the apoptosome and blocks recruitment/activation of caspase-9. This affinity-purified apoptosome complex contained only Apaf-1XL and GST-casp9(1-130), demonstrating that the WD40 and CED-4 domains of Apaf-1 do not stably bind other cytosolic proteins. Next we used a monoclonal antibody to caspase-9 to immunopurify the native active apoptosome complex from cell lysates, containing negligible levels of cytochrome c, second mitochondria-derived activator of caspase (Smac), or Omi/HtrA2. This apoptosome complex exhibited low caspase-processing activity and contained four stably associated proteins, namely Apaf-1, pro-p35/34 forms of caspase-9, pro-p20 forms of caspase-3, X-linked inhibitor of apoptosis (XIAP), and cytochrome c, which was only bound transiently to the complex. However, in lysates containing Smac and Omi/HtrA2, the caspase-processing activity of the purified apoptosome complex increased 6-8-fold and contained only Apaf-1 and the p35/p34-processed subunits of caspase-9. During apoptosis, Smac, Omi/HtrA2, and cytochrome c are released simultaneously from mitochondria, and thus it is likely that the functional apoptosome complex in apoptotic cells consists primarily of Apaf-1 and processed caspase-9.
机译:凋亡小体是激活caspase的大型复合物(约700-1400 kDa),当线粒体依赖性凋亡细胞死亡时释放细胞色素c时,由Apaf-1和caspase-9组装而成。 Apaf-1的核心支架蛋白约为135 kDa,并包含CARD(胱天蛋白酶募集结构域),CED-4和多个(13)WD40重复结构域,这些结构域可能与多种未知的调节蛋白相互作用。为了鉴定此类蛋白质,我们用dATP /细胞色素c激活了THP.1裂解物,并使用了蔗糖密度离心法和基于亲和力的方法纯化了凋亡小体,以进行MALDI-TOF质谱分析。首先,我们使用了谷胱甘肽S-转移酶(GST)融合蛋白(GST-casp9(1-130)),其中包含caspase-9-(1-130)的CARD结构域,该蛋白与Apaf-1的CARD结构域结合它在凋亡小体中,阻止caspase-9的募集/激活。这种亲和纯化的凋亡小体复合物仅包含Apaf-1XL和GST-casp9(1-130),表明Apaf-1的WD40和CED-4域不能稳定地结合其他胞质蛋白。接下来,我们使用了一种针对caspase-9的单克隆抗体,从细胞裂解物中免疫纯化天然的活性凋亡小体复合物,该复合物含有可忽略水平的细胞色素c,第二个线粒体衍生的caspase激活剂(Smac)或Omi / HtrA2。这种凋亡小体复合物显示出低的半胱天冬酶加工活性,并包含四个稳定相关的蛋白质,即Apaf-1,caspase-9的前p35 / 34形式,caspase-3的前p20形式,X连锁凋亡抑制剂(XIAP)和细胞色素c,后者仅短暂地与复合物结合。但是,在含有Smac和Omi / HtrA2的裂解物中,纯化的凋亡小体复合物的caspase加工活性增加了6-8倍,仅包含Apaf-1和caspase-9的p35 / p34处理的亚基。在凋亡过程中,Smac,Omi / HtrA2和细胞色素c同时从线粒体释放,因此凋亡细胞中的功能性凋亡小体复合物可能主要由Apaf-1和加工的caspase-9组成。

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