Allosteric drugs are increasingly used because they produce fewer side effects. Allosteric signal propagation does not stop at the 'end' of a protein, but may be dynamically transmitted across the cell. We propose here that the concept of allosteric drugs can be broadened to 'allo-network drugs' - whose effects can propagate either within a protein, or across several proteins, to enhance or inhibit specific interactions along a pathway. We posit that current allosteric drugs are a special case of allo-network drugs, and suggest that allo-network drugs can achieve specific, limited changes at the systems level, and in this way can achieve fewer side effects and lower toxicity. Finally, we propose steps and methods to identify allo-network drug targets and sites that outline a new paradigm in systems-based drug design.
Allo-network drugs: harnessing allostery in cellular networks.
R. Nussinov,Chung-Jung Tsai,P. Csermely
Published 2011 in TIPS - Trends in Pharmacological Sciences
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PUBLICATION RECORD
- Publication year
2011
- Venue
TIPS - Trends in Pharmacological Sciences
- Publication date
2011-09-23
- Fields of study
Biology, Medicine, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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