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Network Output Controllability-Based Method for Drug Target Identification

机译:基于网络输出可控性的药物靶标识别方法

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摘要

Biomolecules do not perform their functions alone, but interactively with one another to form so called biomolecular networks. It is well known that a complex disease stems from the malfunctions of corresponding biomolecular networks. Therefore, one of important tasks is to identify drug targets from biomolecular networks. In this study, the drug target identification is formulated as a problem of finding steering nodes in biomolecular networks while the concept of network output controllability is applied to the problem of drug target identification. By applying control signals to these steering nodes, the biomolecular networks are expected to be transited from one state to another. A graph-theoretic algorithm has been proposed to find a minimum set of steering nodes in biomolecular networks which can be a potential set of drug targets. Application results of the method to real biomolecular networks show that identified potential drug targets are in agreement with existing research results. This indicates that the method can generate testable predictions and provide insights into experimental design of drug discovery.
机译:生物分子并不单独执行其功能,而是彼此交互形成所谓的生物分子网络。众所周知,复杂的疾病源于相应的生物分子网络的故障。因此,一项重要任务是从生物分子网络中识别药物靶标。在这项研究中,药物目标识别被描述为在生物分子网络中寻找操纵节点的问题,而网络输出可控性的概念则被应用于药物目标识别的问题。通过将控制信号施加到这些转向节点,生物分子网络有望从一种状态转换到另一种状态。已经提出了一种图论算法来寻找生物分子网络中最小的指导节点集,该指导集可以是潜在的药物靶标集。该方法在实际生物分子网络中的应用结果表明,确定的潜在药物靶标与现有研究结果一致。这表明该方法可以生成可检验的预测结果,并提供有关药物发现实验设计的见识。

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