Computational modeling of subcellular transport and signaling.

Computational modeling of subcellular transport and signaling.
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DOI:
10.1016/j.sbi.2014.01.006
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发表时间:
2014-04
影响因子:
6.8
通讯作者:
McCulloch AD
McCulloch AD
中科院分区:
生物学2区
文献类型:
--
作者:
Hake J;Kekenes-Huskey PM;McCulloch AD

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细胞中的许多信号传导过程是在微结构域中控制的,微结构域由细胞结构定义,大小从nm到µm不等。最近显微镜技术的改进使这些微结构域的分辨率和重建成为可能,而新的计算方法为阐明它们的功能作用提供了手段。总的来说,这些工具允许对细胞环境及其在疾病中的病理进展进行生物物理理解。在这里,我们回顾了显微镜和基于重建几何的亚细胞建模的最新进展,特别关注对心肌细胞兴奋收缩耦合很重要的信号微域。
Numerous signaling processes in the cell are controlled in microdomains that are defined by cellular structures ranging from nm to µm in size. Recent improvements in microscopy enable the resolution and reconstruction of these micro domains, while new computational methods provide the means to elucidate their functional roles. Collectively these tools allow for a biophysical understanding of the cellular environment and its pathological progression in disease. Here we review recent advancements in microscopy, and subcellular modeling based on reconstructed geometries, with a special focus on signaling microdomains that are important for the excitation contraction coupling in cardiac myocytes.
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