Allo-Network Drugs: Extension of the Allosteric Drug Concept to Protein-Protein Interaction and Signaling Networks
被引:59
作者:
Szilagyi, Andras
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Semmelweis Univ, Dept Med Chem, H-1444 Budapest 8, Hungary
Res Ctr Nat Sci, Inst Enzymol, H-1113 Budapest, HungarySemmelweis Univ, Dept Med Chem, H-1444 Budapest 8, Hungary
Szilagyi, Andras
[1
,2
]
Nussinov, Ruth
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NCI, Ctr Canc Res, SAIC Frederick Inc, Frederick Natl Lab Canc Res,Nanobiol Program, Frederick, MD 21702 USA
Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, Sackler Inst Mol Med, IL-69978 Tel Aviv, IsraelSemmelweis Univ, Dept Med Chem, H-1444 Budapest 8, Hungary
Nussinov, Ruth
[3
,4
]
Csermely, Peter
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Semmelweis Univ, Dept Med Chem, H-1444 Budapest 8, HungarySemmelweis Univ, Dept Med Chem, H-1444 Budapest 8, Hungary
Csermely, Peter
[1
]
机构:
[1] Semmelweis Univ, Dept Med Chem, H-1444 Budapest 8, Hungary
[2] Res Ctr Nat Sci, Inst Enzymol, H-1113 Budapest, Hungary
[3] NCI, Ctr Canc Res, SAIC Frederick Inc, Frederick Natl Lab Canc Res,Nanobiol Program, Frederick, MD 21702 USA
[4] Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, Sackler Inst Mol Med, IL-69978 Tel Aviv, Israel
Allosteric drugs are usually more specific and have fewer side effects than orthosteric drugs targeting the same protein. Here, we overview the current knowledge on allosteric signal transmission from the network point of view, and show that most intra-protein conformational changes may be dynamically transmitted across protein-protein interaction and signaling networks of the cell. Allo-network drugs influence the pharmacological target protein indirectly using specific inter-protein network pathways. We show that allo-network drugs may have a higher efficiency to change the networks of human cells than those of other organisms, and can be designed to have specific effects on cells in a diseased state. Finally, we summarize possible methods to identify allo-network drug targets and sites, which may develop to a promising new area of systems-based drug design.