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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Non-bilayer structures in mitochondrial membranes regulate ATP synthase activity
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Non-bilayer structures in mitochondrial membranes regulate ATP synthase activity

机译:线粒体膜中的非双层结构调节ATP合成酶活性

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摘要

Abstract Cardiolipin (CL) is an anionic phospholipid at the inner mitochondrial membrane (IMM) that facilitates the formation of transient non-bilayer (non-lamellar) structures to maintain mitochondrial integrity. CL modulates mitochondrial functions including ATP synthesis. However, the biophysical mechanisms by which CL generates non-lamellar structures and the extent to which these structures contribute to ATP synthesis remain unknown. We hypothesized that CL and ATP synthase facilitate the formation of non-bilayer structures at the IMM to stimulate ATP synthesis. By using 1 H NMR and 31 P NMR techniques, we observed that increasing the temperature (8°C to 37°C), lowering the pH (3.0), or incubating intact mitochondria with CTII - an IMM-targeted toxin that increases the formation of immobilized non-bilayer structures - elevated the formation of non-bilayer structures to stimulate ATP synthesis. The F 0 sector of the ATP synthase complex can facilitate the formation of non-bilayer structures as incubating model membranes enriched with IMM-specific phospholipids with exogenous DCCD-binding protein of the F 0 sector (DCCD-BPF) elevated the formation of immobilized non-bilayer structures to a similar manner as CTII. Native PAGE assays revealed that CL, but not other anionic phospholipids, specifically binds to DCCD-BPF to promote the formation of stable lipid-protein complexes. Mechanistically, molecular docking studies identified two lipid binding sites for CL in DCCD-BPF. We propose a new model of ATP synthase regulation in which CL mediates the formation of non-bilayer structures that serve to cluster protons and ATP synthase complexes as a mechanism to enhance proton translocation to the F 0 sector, and thereby increase ATP synthesis. Graphical abstract Display Omitted Highlights ? Changes in pH modulate the formation of non-bilayer structures in model membranes ? Non-bilayer structures, including inverted micelles, regulate ATP synthesis. ? Cardiolipin facilitates the formation of non-bilayer structures. ? DCCD-binding protein of F 0 sector augments the formation of non-bilayer structures ? CL binds to the DCCD-binding protein of the F 0 sector
机译:摘要心肌(CL)是内部线粒体膜(IMM)处的阴离子磷脂,便于形成瞬时非双层(非层层)结构以保持线粒体完整性。 CL调节线粒体功能,包括ATP合成。然而,CL产生非层状结构的生物物理机制以及这些结构贡献到ATP合成的程度仍然未知。我们假设Cl和ATP合酶有助于在IMM中形成非双层结构以刺激ATP合成。通过使用1 H NMR和31 P NMR技术,我们观察到将温度(8℃至37℃)增加,降低pH(3.0),或用CTII孵育完整的线粒体 - 一种增加形成的Imm-靶向毒素固定化的非双层结构 - 升高了非双层结构的形成刺激ATP合成。 ATP合酶复合物的F 0扇区可以促进非双层结构的形成,因为将模型膜培养与具有F 0扇区的外源性DCCD结合蛋白(DCCD-BPF)的外源性DCCD结合蛋白升高,升高了固定的非 - 单层结构与CTII类似的方式。本机页面测定显示CL,但不是其他阴离子磷脂,特异性结合DCCD-BPF,促进稳定的脂质蛋白复合物的形成。机械地,分子对接研究鉴定了DCCD-BPF中CL的两种脂质结合位点。我们提出了一种新的ATP合酶调节模型,其中Cl介导非双层结构的形成,所述非双层结构的形成,所述非双层结构用于将质子和ATP合酶复合物作为增强质子易位到F 0扇区的机制,从而增加ATP合成。图形抽象显示省略了亮点? pH的变化调节模型膜中非双层结构的形成吗?非双层结构,包括倒胶束,调节ATP合成。还心肺素有助于形成非双层结构。还F 0扇区的DCCD结合蛋白增强了非双层结构的形成? CL与F 0扇区的DCCD结合蛋白结合

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