Department of Physiology, University of Maryland School of Medicine, Baltimore, Maryland.
Department of Physiology, University of Maryland School of Medicine, Baltimore, Maryland.
Biophys J. 2024 Aug 20;123(16):2392-2405. doi: 10.1016/j.bpj.2024.05.024. Epub 2024 May 24.
hERG potassium channels are critical for cardiac excitability. hERG channels have a Per-Arnt-Sim (PAS) domain at their N-terminus, and here, we examined the mechanism for PAS domain regulation of channel opening and closing (gating). We used TAG codon suppression to incorporate the noncanonical amino acid 4-benzoyl-L-phenylalanine (BZF), which is capable of forming covalent cross-links after photoactivation by ultraviolet (UV) light, at three locations (G47, F48, and E50) in the PAS domain. We found that hERG-G47BZF channels had faster closing (deactivation) when irradiated in the open state (at 0 mV) but showed no measurable changes when irradiated in the closed state (at -100 mV). hERG-F48BZF channels had slower activation, faster deactivation, and a marked rightward shift in the voltage dependence of activation when irradiated in the open (at 0 mV) or closed (at -100 mV) state. hERG-E50BZF channels had no measurable changes when irradiated in the open state (at 0 mV) but had slower activation, faster deactivation, and a rightward shift in the voltage dependence of activation when irradiated in the closed state (at -100mV), indicating that hERG-E50BZF had a state-dependent difference in UV photoactivation, which we interpret to mean that PAS underwent molecular motions between the open and closed states. Moreover, we propose that UV-dependent biophysical changes in hERG-G47BZF, F48BZF, and E50BZF were the direct result of photochemical cross-linking that reduced dynamic motions in the PAS domain and broadly stabilized the closed state relative to the open state of the channel.
hERG 钾通道对于心脏兴奋性至关重要。hERG 通道在其 N 端具有一个 Per-Arnt-Sim(PAS)结构域,在此,我们研究了 PAS 结构域调节通道开放和关闭(门控)的机制。我们使用 TAG 密码子抑制技术将非天然氨基酸 4-苯甲酰-L-苯丙氨酸(BZF)引入 PAS 结构域的三个位置(G47、F48 和 E50),BZF 在经紫外线(UV)光光激活后能够形成共价交联。我们发现,当 hERG-G47BZF 通道在开放状态(在 0 mV 时)被照射时,其关闭(失活)更快,但当在关闭状态(在-100 mV 时)被照射时,没有可测量的变化。hERG-F48BZF 通道的激活速度较慢,失活速度较快,当在开放(在 0 mV 时)或关闭(在-100 mV 时)状态下被照射时,激活的电压依赖性有明显的右移。hERG-E50BZF 通道在开放状态(在 0 mV 时)被照射时没有可测量的变化,但在关闭状态(在-100 mV 时)被照射时激活速度较慢,失活速度较快,激活的电压依赖性向右移动,表明 hERG-E50BZF 在 UV 光激活方面存在状态依赖性差异,我们将其解释为 PAS 在开放和关闭状态之间发生了分子运动。此外,我们提出 hERG-G47BZF、F48BZF 和 E50BZF 的 UV 依赖性生物物理变化是 PAS 结构域中光化学交联的直接结果,该交联减少了 PAS 结构域的动态运动,并相对于通道的开放状态广泛稳定了关闭状态。