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From Systems to Structure: ridging Networks and Mechanism

期刊

MOLECULAR CELL
卷 49, 期 2, 页码 222-231

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2013.01.003

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资金

  1. NIH [DP50D009180, GM081879, GM078360, GM084448, GM082250, GM084279, GM098101, Al090935, Al091575]
  2. DARPA [HR0011-11-C-0094]

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There is a wide gap between the generation of large-scale biological data sets and more-detailed, structural and mechanistic studies. However, recent studies that explicitly combine data from systems and structural biological approaches are having a profound effect on our ability to predict how mutations and small molecules affect atomic-level mechanisms, disrupt systems-level networks, and ultimately lead to changes in organismal fitness. In fact, we argue that a shared framework for analysis of nonadditive genetic and thermodynamic responses to perturbations will accelerate the integration of reductionist and global approaches. A stronger bridge between these two areas will allow for a deeper and more-complete understanding of complex biological phenomenon and ultimately provide needed breakthroughs in biomedical research.

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