首页> 外文期刊>Biophysical Journal >Exact Stochastic Simulation of a Calcium Microdomain Reveals the Impact of Ca2+ Fluctuations on IP3R Gating
【24h】

Exact Stochastic Simulation of a Calcium Microdomain Reveals the Impact of Ca2+ Fluctuations on IP3R Gating

机译:钙微米瘤的精确随机模拟显示了CA2 +波动对IP3R门控的影响

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

In this study, we numerically analyzed the nonlinear Ca2+-dependent gating dynamics of a single, nonconducting inositol 1,4,5-trisphosphate receptor (IP3R) channel, using an exact and fully stochastic simulation algorithm that includes channel gating, Ca2+ buffering, and Ca2+ diffusion. The IP3R is a ubiquitous intracellular Ca2+ release channel that plays an important role in the formation of complex spatiotemporal Ca2+ signals such as waves and oscillations. Dynamic subfemtoliter Ca2+ microdomains reveal low copy numbers of Ca2+ ions, buffer molecules, and IP(3)Rs, and stochastic fluctuations arising from molecular interactions and diffusion do not average out. In contrast to models treating calcium dynamics deterministically, the stochastic approach accounts for this molecular noise. We varied Ca2+ diffusion coefficients and buffer reaction rates to tune the autocorrelation properties of Ca2+ noise and found a distinct relation between the autocorrelation time tau(ac), the mean channel open and close times, and the resulting IP3R open probability PO. We observed an increased PO for shorter noise autocorrelation times, caused by increasing channel open times and decreasing close times. In a pure diffusion model the effects become apparent at elevated calcium concentrations, e.g., at [Ca2+] = 25 mu M, tau(ac) = 0.082 ms, the IP3R open probability increased by approximate to 20% and mean open times increased by approximate to 4 ms, compared to a zero noise model. We identified the inactivating Ca2+ binding site of IP3R subunits as the primarily noise-susceptible element of the De Young and Keizer model. Short Ca2+ noise autocorrelation times decrease the probability of Ca2+ association and consequently increase IP3R activity. These results suggest a functional role of local calcium noise properties on calcium-regulated target molecules such as the ubiquitous IP3R. This finding may stimulate novel experimental approaches analyzing the role of calcium noise properties on microdomain behavior.
机译:在该研究中,我们使用精确和完全随机仿真算法在数值分析了单个非导电肌醇1,4,5-三磷酸盐受体(IP3R)通道的非线性CA2 +型依赖性浇注动力学。包括渠道门控,CA2 +缓冲和CA2 +扩散。 IP3R是一种普遍存在的细胞内Ca2 +释放通道,其在诸如波和振荡的复杂时空CA2 +信号的形成中起重要作用。动态亚次渗溶发酸剂CA2 +微滴显示Ca2 +离子,缓冲分子和IP(3)Rs的低拷贝数,并且来自分子相互作用和扩散产生的随机波动不均匀。与各种模型处理钙动力学的模型,随机方法占该分子噪声。我们改变了CA2 +扩散系数和缓冲反应速率,以调整CA2 +噪声的自相关性能,发现自相关时间TAU(AC),平均通道打开和关闭时间之间的不同关系,以及所得到的IP3R开放概率PO。我们观察到较短的噪声自相关时间增加的PO,通过增加信道开放时间和关闭时光引起。在纯的扩散模型中,钙浓度的效果变得显而易见,例如,在[Ca2 +] =25μm,tau(Ac)= 0.082ms,IP3R开放概率通过近似增加20%,平均开放时间增加与零噪声模型相比,至4 ms。我们将IP3R亚基的灭活CA2 +绑定站点鉴定为DE YOUNG和Keizer模型的主要噪声易感元素。短CA2 +噪声自相关时间降低CA2 +关联的概率,从而增加IP3R活动。这些结果表明局部钙噪声特性在钙调节靶分子(如普遍存在的IP3R)上的功能作用。该发现可能刺激新的实验方法分析钙噪声特性对微米瘤行为的作用。

著录项

  • 来源
    《Biophysical Journal》 |2015年第3期|共11页
  • 作者单位

    Heidelberg Univ Dept Physiol &

    Pathophysiol Med Biophys Unit Heidelberg Germany;

    Heidelberg Univ Dept Physiol &

    Pathophysiol Med Biophys Unit Heidelberg Germany;

    Heidelberg Univ Dept Physiol &

    Pathophysiol Med Biophys Unit Heidelberg Germany;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物物理学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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