首页> 美国卫生研究院文献>Biophysical Journal >C-Terminal Modulatory Domain Controls Coupling of Voltage-Sensing to Pore Opening in Cav1.3 L-type Ca2+ Channels
【2h】

C-Terminal Modulatory Domain Controls Coupling of Voltage-Sensing to Pore Opening in Cav1.3 L-type Ca2+ Channels

机译:C端子调制域控制Cav1.3 L型Ca2 +通道中电压感应与孔开放的耦合

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Activity of voltage-gated Cav1.3 L-type Ca2+ channels is required for proper hearing as well as sinoatrial node and brain function. This critically depends on their negative activation voltage range, which is further fine-tuned by alternative splicing. Shorter variants miss a C-terminal regulatory domain (CTM), which allows them to activate at even more negative potentials than C-terminally long-splice variants. It is at present unclear whether this is due to an increased voltage sensitivity of the Cav1.3 voltage-sensing domain, or an enhanced coupling of voltage-sensor conformational changes to the subsequent opening of the activation gate. We studied the voltage-dependence of voltage-sensor charge movement (QON-V) and of current activation (ICa-V) of the long (Cav1.3L) and a short Cav1.3 splice variant (Cav1.342A) expressed in tsA-201 cells using whole cell patch-clamp. Charge movement (QON) of Cav1.3L displayed a much steeper voltage-dependence and a more negative half-maximal activation voltage than Cav1.2 and Cav3.1. However, a significantly higher fraction of the total charge had to move for activation of Cav1.3 half-maximal conductance (Cav1.3: 68%; Cav1.2: 52%; Cav3.1: 22%). This indicated a weaker coupling of Cav1.3 voltage-sensor charge movement to pore opening. However, the coupling efficiency was strengthened in the absence of the CTM in Cav1.342A, thereby shifting ICa-V by 7.2 mV to potentials that were more negative without changing QON-V. We independently show that the presence of intracellular organic cations (such as n-methyl-D-glucamine) induces a pronounced negative shift of QON-V and a more negative activation of ICa-V of all three channels. These findings illustrate that the voltage sensors of Cav1.3 channels respond more sensitively to depolarization than those of Cav1.2 or Cav3.1. Weak coupling of voltage sensing to pore opening is enhanced in the absence of the CTM, allowing short Cav1.342A splice variants to activate at lower voltages without affecting QON-V.
机译:电压门控的Cav1.3 L型Ca 2 + 通道的活动是正常听力以及窦房结和脑功能所必需的。这主要取决于它们的负激活电压范围,该范围可通过替代拼接进一步微调。较短的变异体缺少C末端调节域(CTM),这使它们可以比C末端长​​剪接变异体以更高的负电位激活。目前尚不清楚这是否是由于Cav1.3电压感应域的电压灵敏度增加,还是由于电压传感器构象变化与激活栅极的后续打开之间的耦合增强所致。我们研究了以tsA表示的长(Cav1.3L)和短Cav1.3剪接变体(Cav1.342A)的电压传感器电荷移动(QON-V)和电流激活(ICa-V)的电压相关性-201细胞使用全细胞膜片钳。与Cav1.2和Cav3.1相比,Cav1.3L的电荷移动(QON)显示出更陡峭的电压依赖性和更大的负半最大激活电压。但是,为了激活Cav1.3半最大电导,必须移动总电荷中较高的一部分(Cav1.3:68%; Ca v 1.2:52%; Ca v 3.1:22%)。这表明Ca v 1.3电压传感器电荷运动与开孔之间的耦合较弱。但是,在Ca v 1.3 42A 中不存在CTM的情况下,耦合效率得到了增强,从而使I Ca -V偏移7.2mV至不改变Q ON -V的负电位。我们独立地表明,细胞内有机阳离子(例如n-甲基-D-葡糖胺)的存在会引起Q ON -V明显的负移,而I Ca < / sub> -V的所有三个通道。这些发现说明,Ca v 1.3通道的电压传感器对去极化的响应比Ca v 1.2或Ca v 3.1的要敏感。在不存在CTM的情况下,电压感应与开孔的弱耦合得以增强,从而允许短的Ca v 1.3 42A 剪接变体在较低的电压下激活而不会影响Q -V。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号