AKAP350C通过一种新的两性α螺旋结构域靶向线粒体。

Cellular logistics Pub Date : 2014-07-03 eCollection Date: 2014-07-01 DOI:10.4161/21592780.2014.943597
Twila A Mason, James R Goldenring, Elena Kolobova
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引用次数: 3

摘要

线粒体调节细胞内的代谢和体内平衡。线粒体也是非常动态的细胞器,不断经历裂变和融合。在与这些过程中的缺陷相关的各种疾病中,维持适当的线粒体动力学的重要性是显而易见的。蛋白激酶A (PKA)是线粒体动力学的关键调节因子。PKA受a激酶锚定蛋白(AKAPs)的空间调控。我们完成了一种新的AKAP350亚型AKAP350C的克隆。内源性AKAP350C免疫染色显示定位于线粒体。AKAP350C独有的羧基末端54个氨基酸序列包含一个新的两亲性α螺旋线粒体靶向结构域。AKAP350C与Mff(线粒体裂变蛋白)和mitofusins 1和2(线粒体融合蛋白)共定位,可能通过支架PKA和线粒体裂变融合蛋白调控线粒体动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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AKAP350C targets to mitochondria via a novel amphipathic alpha helical domain.

Mitochondria regulate metabolism and homeostasis within cells. Mitochondria are also very dynamic organelles, constantly undergoing fission and fusion. The importance of maintaining proper mitochondrial dynamics is evident in the various diseases associated with defects in these processes. Protein kinase A (PKA) is a key regulator of mitochondrial dynamics. PKA is spatially regulated by A-Kinase Anchoring Proteins (AKAPs). We completed cloning of a novel AKAP350 isoform, AKAP350C. Immunostaining for endogenous AKAP350C showed localization to mitochondria. The carboxyl-terminal 54-amino acid sequence unique to AKAP350C contains a novel amphipathic alpha helical mitochondrial-targeting domain. AKAP350C co-localizes with Mff (mitochondrial fission protein) and mitofusins 1 and 2 (mitochondrial fusion proteins), and likely regulates mitochondrial dynamics by scaffolding PKA and mitochondrial fission and fusion proteins.

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