Centre for Molecular Simulation, University of Calgary, Calgary, AB T2N 1N4, Canada.
Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1N4, Canada.
Proc Natl Acad Sci U S A. 2022 Mar 29;119(13):e2109431119. doi: 10.1073/pnas.2109431119. Epub 2022 Mar 25.
SignificanceCholesterol is one of the main components found in plasma membranes and is involved in lipid-dependent signaling enabled by integral membrane proteins such as inwardly rectifying potassium (Kir) channels. Similar to other ion channels, most of the Kir channels are down-regulated by cholesterol. One of the very few notable exceptions is Kir3.4, which is up-regulated by this important lipid. Here, we discovered and characterized a molecular switch that controls the impact (up-regulation vs. down-regulation) of cholesterol on Kir3.4. Our results provide a detailed molecular mechanism of tunable cholesterol regulation of a potassium channel.
意义胆固醇是质膜中的主要成分之一,参与由整合膜蛋白(如内向整流钾 (Kir) 通道)介导的脂质依赖性信号转导。与其他离子通道类似,大多数 Kir 通道受胆固醇下调。Kir3.4 是一个非常少见的例外,它受这种重要脂质的上调。在这里,我们发现并描述了一个分子开关,该开关控制了胆固醇对 Kir3.4 的影响(上调与下调)。我们的结果提供了钾通道可调节胆固醇调节的详细分子机制。