首页> 外文会议>International Conference on Parallel Problem Solving from Nature(PPSN VIII); 20040918-22; Birmingham(GB) >A Novel Programmable Molecular Computing Method Based on Signaling Pathways Regulated by Rho-GTPases in Living MDCK Epithelial Mammalian Cells
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A Novel Programmable Molecular Computing Method Based on Signaling Pathways Regulated by Rho-GTPases in Living MDCK Epithelial Mammalian Cells

机译:基于Rho-GTPases调节MDCK上皮哺乳动物细胞信号通路的新型可编程分子计算方法

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In this paper, we propose a new biomolecular computing method based on the crosstalked pathways of living cells and the corresponding kinase-phosphatase networks under the regulation of Rho family GTPases. Owing to their merits of efficient regulation in controlled pathway complexity and low cost in implementation, we propose a feasible protocol (the algorithm) for kinase-and-phosphatase-based computers (called kinase computers for short) and the materials and methods for their implementation. In order to obtain high programmability in molecular computation, we have successfully designed pathway regulation schemes for computation. Here we report our latest simulation results on a designed controllable crosstalk mechanism and efficient schemes for engineered GTPase-based signaling communications for stable kinase computing under the dynamical environment of a cell culture assay. This is significant for the application of molecular computing to medical nano-bioinformatics and also provides a testbed for new and unconventional computing paradigms inspired by nature.
机译:在本文中,我们提出了一种新的生物分子计算方法,该方法基于活细胞的串扰通路和Rho家族GTPases的调控下相应的激酶磷酸酶网络。由于它们具有有效控制途径复杂度和实施成本低的优点,我们提出了一种基于激酶和磷酸酶的计算机(简称为激酶计算机)的可行协议(算法)及其实施的材料和方法。为了在分子计算中获得高度可编程性,我们成功设计了用于计算的途径调控方案。在这里,我们将报告有关设计可控串扰机制和针对基于GTPa​​se的信号通讯的有效方案的最新模拟结果,以在细胞培养测定的动态环境下稳定激酶计算。这对于分子计算在医学纳米生物信息学中的应用具有重要意义,也为受自然启发的新型和非常规计算范例提供了试验平台。

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