Department of Pharmacology and Physiology, University of Rochester, Rochester, NY 14642, United States of America.
Department of Pharmacology and Physiology, University of Rochester, Rochester, NY 14642, United States of America.
Biochim Biophys Acta Mol Cell Res. 2018 Nov;1865(11 Pt B):1698-1706. doi: 10.1016/j.bbamcr.2018.07.004. Epub 2018 Jul 17.
Ion channels are pore-forming protein complexes in membranes that play essential roles in a diverse array of biological activities. Ion channel activity is strictly regulated at multiple levels and by numerous cellular events to selectively activate downstream effectors involved in specific biological activities. For example, ions, binding proteins, nucleotides, phosphorylation, the redox state, channel subunit composition have all been shown to regulate channel activity and subsequently allow channels to participate in distinct cellular events. While these forms of modulation are well documented and have been extensively reviewed, in this article, we will first review and summarize channel proteolysis as a novel and quite widespread mechanism for altering channel activity. We will then highlight the recent findings demonstrating that proteolysis profoundly alters Inositol 1,4,5 trisphosphate receptor activity, and then discuss its potential functional ramifications in various developmental and pathological conditions.
离子通道是膜中的孔形成蛋白复合物,在各种生物活性中起着至关重要的作用。离子通道活性在多个水平和多种细胞事件中受到严格调节,以选择性地激活参与特定生物活性的下游效应器。例如,已经表明离子、结合蛋白、核苷酸、磷酸化、氧化还原状态、通道亚基组成都可以调节通道活性,从而使通道参与不同的细胞事件。虽然这些形式的调节已经得到很好的记录和广泛的综述,但在本文中,我们将首先回顾和总结通道蛋白水解作为一种改变通道活性的新的和相当普遍的机制。然后,我们将强调最近的发现,证明蛋白水解深刻地改变了肌醇 1,4,5 三磷酸受体的活性,然后讨论其在各种发育和病理条件下的潜在功能后果。