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Kv1.3通道的线粒体定位

The Mitochondrial Routing of the Kv1.3 Channel.

作者信息

Capera Jesusa, Navarro-Pérez María, Moen Anne Stine, Szabó Ildiko, Felipe Antonio

机构信息

Molecular Physiology Laboratory, Dpt. de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, Barcelona, Spain.

Kennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.

出版信息

Front Oncol. 2022 Mar 24;12:865686. doi: 10.3389/fonc.2022.865686. eCollection 2022.

Abstract

Voltage-gated potassium channels control neuronal excitability and cardiac action potentials. In addition, these proteins are involved in a myriad of cellular processes. The potassium channel Kv1.3 plays an essential role in the immune response mediated by leukocytes. Kv1.3 is functional both at the plasma membrane and the inner mitochondrial membrane. Plasma membrane Kv1.3 mediates cellular activation and proliferation, whereas mitochondrial Kv1.3 participates in cell survival and apoptosis. Therefore, this protein emerges as an important target in cancer therapies. Several forward-traffic motifs target the channel to the plasma membrane in a COPII-dependent manner. However, the mitochondrial import pathway for Kv1.3 is largely unknown. Here, we deciphered the mitochondrial routing of the mitoKv1.3 channel. Kv1.3 uses the TIM23 complex to translocate to the inner mitochondrial membrane. This mechanism is unconventional because the channel is a multimembrane spanning protein without a defined N-terminal presequence. We found that transmembrane domains cooperatively mediate Kv1.3 mitochondrial targeting and identified the cytosolic HSP70/HSP90 chaperone complex as a key regulator of the process. Our results provide insights into the mechanisms mediating the localization of Kv1.3 to mitochondrial membranes, further extending the knowledge of ion channel biogenesis and turnover in mitochondria.

摘要

电压门控钾通道控制神经元兴奋性和心脏动作电位。此外,这些蛋白质还参与众多细胞过程。钾通道Kv1.3在白细胞介导的免疫反应中起重要作用。Kv1.3在质膜和线粒体内膜上均有功能。质膜Kv1.3介导细胞活化和增殖,而线粒体Kv1.3参与细胞存活和凋亡。因此,这种蛋白质成为癌症治疗中的一个重要靶点。几个正向运输基序以COPII依赖的方式将该通道靶向质膜。然而,Kv1.3的线粒体导入途径在很大程度上尚不清楚。在这里,我们破译了线粒体Kv1.3通道的线粒体转运途径。Kv1.3利用TIM23复合体转运到线粒体内膜。这种机制是非传统的,因为该通道是一种跨多膜的蛋白质,没有明确的N端前序列。我们发现跨膜结构域协同介导Kv1.3的线粒体靶向,并确定胞质HSP70/HSP90伴侣复合体是该过程的关键调节因子。我们的结果为介导Kv1.3定位于线粒体膜的机制提供了见解,进一步扩展了线粒体中离子通道生物发生和周转的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d28/8990977/746388bad7cb/fonc-12-865686-g001.jpg

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