Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, UNAM. Av. Universidad 2001, Cuernavaca, Morelos, México.
Instituto Gulbenkian de Ciência. Rua da Quinta Grande 6, Oeiras, Portugal.
Channels (Austin). 2021 Dec;15(1):424-437. doi: 10.1080/19336950.2021.1919463.
The mitochondrial BK channel (mitoBK) is a splice variant of plasma membrane BK (Maxi-K, BK, Slo1, K1.1). While a high-resolution structure of mitoBK is not available yet, functional and structural studies of the plasma membrane BK have provided important clues on the gating of the channel by voltage and Ca, as well as the interaction with auxiliary subunits. To date, we know that the control of expression of mitoBK, targeting and voltage-sensitivity strongly depends on its association with its regulatory β1-subunit, which overall participate in the control of mitochondrial Ca-overload in cardiac myocytes. Moreover, novel regulatory mechanisms of mitoBK such as β-subunits and amyloid-β have recently been proposed. However, major basic questions including how the regulatory BK-β1-subunit reaches mitochondria and the mechanism through which amyloid-β impairs mitoBK channel function remain to be addressed.
线粒体 BK 通道(mitoBK)是质膜 BK(Maxi-K、BK、Slo1、K1.1)的剪接变体。虽然尚未获得 mitoBK 的高分辨率结构,但对质膜 BK 的功能和结构研究为电压和 Ca 对通道门控的作用以及与辅助亚基的相互作用提供了重要线索。迄今为止,我们知道 mitoBK 的表达调控、靶向和电压敏感性强烈依赖于其与调节性 β1 亚基的结合,β1 亚基总体上参与了心肌细胞中线粒体钙超载的控制。此外,最近还提出了 mitoBK 的新型调节机制,如 β 亚基和淀粉样β。然而,包括调节性 BK-β1 亚基如何到达线粒体以及淀粉样β如何损害 mitoBK 通道功能的机制等主要基本问题仍有待解决。