Wu Lin, Tang Lingkai, Li Min, Wang Jianxin, Wu Fang-Xiang
IEEE Trans Nanobioscience. 2017 Jul;16(5):326-332. doi: 10.1109/TNB.2017.2705106.
Complex networks are ubiquitous in nature. In biological systems, biomolecules interact with each other to form so-called biomolecular networks, which determine the cellular behaviors of living organisms. Controlling the cellular behaviors by regulating certain biomolecules in the network is one of the most concerned problems in systems biology. Recently, the connections between biological networks and structural control theory have been explored, uncovering some interesting biological phenomena. Some researchers have paid attentions to the structural controllability of networks in notion of the minimum steering sets (MSSs). However, because the MSSs for complex networks are not unique and the importance of different MSSs is diverse in real applications, MSSs with certain meanings should be studied. In this paper, we investigated the MSSs of biomolecular networks by considering the drug binding information. The biomolecules in the MSSs with binding preference are enriched with known drug targets and are likely to have more chemical-binding opportunities with existing drugs compared with randomly chosen MSSs, suggesting novel applications for drug target identification and drug repositioning.
复杂网络在自然界中无处不在。在生物系统中,生物分子相互作用形成所谓的生物分子网络,这些网络决定了生物体的细胞行为。通过调节网络中的某些生物分子来控制细胞行为是系统生物学中最受关注的问题之一。最近,人们探索了生物网络与结构控制理论之间的联系,发现了一些有趣的生物学现象。一些研究人员从最小转向集(MSS)的概念出发关注网络的结构可控性。然而,由于复杂网络的MSS不唯一,且不同MSS在实际应用中的重要性各不相同,因此应研究具有特定意义的MSS。在本文中,我们通过考虑药物结合信息来研究生物分子网络的MSS。与随机选择的MSS相比,具有结合偏好的MSS中的生物分子富含已知药物靶点,并且可能与现有药物有更多的化学结合机会,这为药物靶点识别和药物重新定位提供了新的应用。