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Profiling the Nanoparticles Associated Protein-protein Interactions
被引:0
|作者:
Liao, Wei-Chen
[1
]
Huang, Nai-Kuei
[2
]
机构:
[1] Natl Taitung Univ, Dept Appl Sci, Taitung, Taiwan
[2] Natl Res Inst Chinese Med, Taipei, Taiwan
关键词:
nanoparticles;
bioinformatics;
complex networks;
NETWORKS;
D O I:
10.1109/BIBE.2009.54
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
To explore the nanoparticles-dependent signaling pathways is a rapidly growing research field. Here, we globally elucidate the regulation modules of cellular molecules by using graph-based representation of complex networks. We have packed some useful bioinformatics methods (Matlab Simbiology and Pathway Studio) into an integrated system for graph-based representation and complex networks modeling. Here, this system is applied to the public literature and microarray database of nanoparticles and try to find out nanoparticles related genetic regulatory pathways. By comparing to different model organism system (bacteria, mice, cell line), we will establish a multidimensional (protein cellular location, time course expression pattern and chemicals interacting profiles) secondary database. The value added database will uncover some new relationships between genes and nanoparticles and provide useful information for the modeling of nanoparticles cellular regulatory pathway in an interactive form. The new modeling approaches should serve as a research platform to find protein candidates for nanoparticles associated diseases and provides a possible cue to improve the bio-chemo-informatics analyses on gene expression and molecular pharmacology.
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页码:382 / +
页数:3
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