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Lifetime imaging of GFP at CoxVIIIa reports respiratory supercomplex assembly in live cells

机译:GFP在CoxVIIIa上的终身成像报告了活细胞中的呼吸超复合体组装

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摘要

The assembly of respiratory complexes into macromolecular supercomplexes is currently a hot topic, especially in the context of newly available structural details. However, most work to date has been done with purified detergent-solubilized material and in situ confirmation is absent. We here set out to enable the recording of respiratory supercomplex formation in living cells. Fluorescent sensor proteins were placed at specific positions at cytochrome c oxidase suspected to either be at the surface of a CI1CIII2CIV1 supercomplex or buried within this supercomplex. In contrast to other loci, sensors at subunits CoxVIIIa and CoxVIIc reported a dense protein environment, as detected by significantly shortened fluorescence lifetimes. According to 3D modelling CoxVIIIa and CoxVIIc are buried in the CI1CIII2CIV1 supercomplex. Suppression of supercomplex scaffold proteins HIGD2A and CoxVIIa2l was accompanied by an increase in the lifetime of the CoxVIIIa-sensor in line with release of CIV from supercomplexes. Strikingly, our data provide strong evidence for defined stable supercomplex configuration in situ.
机译:将呼吸复合物组装成大分子超复合物目前是一个热门话题,尤其是在新近可获得的结构细节中。然而,迄今为止,大多数工作都是用纯化的去污剂增溶的材料完成的,并且没有现场确认。我们在这里着手记录活细胞中呼吸超复合物的形成。荧光传感器蛋白被放置在细胞色素C氧化酶的特定位置,怀疑是在CI1CIII2CIV1超复合物的表面或埋在该超复合物中。与其他基因座相反,亚基CoxVIIIa和CoxVIIc的传感器报告了密集的蛋白质环境,这可以通过明显缩短的荧光寿命来检测。根据3D建模,CoxVIIIa和CoxVIIc被埋在CI1CIII2CIV1超复合物中。抑制超复杂支架蛋白HIGD2A和CoxVIIa21伴随着CoxVIIIa传感器寿命的增加,与超复合物中CIV的释放相一致。令人惊讶的是,我们的数据为就地定义的稳定超复杂构型提供了有力的证据。

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