Allo-Network Drugs: Extension of the Allosteric Drug Concept to Protein-Protein Interaction and Signaling Networks

被引:59
作者
Szilagyi, Andras [1 ,2 ]
Nussinov, Ruth [3 ,4 ]
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
基金
美国国家科学基金会;
关键词
Allo-network drugs; allosteric drugs; interactome; protein-protein interaction networks; protein structure networks; signaling networks; TRANSFER-RNA SYNTHETASE; AMINO-ACID; MOLECULAR-DYNAMICS; DIHYDROFOLATE-REDUCTASE; CONTACT NETWORKS; ANALYSIS REVEALS; NATIVE PROTEINS; ENERGY-TRANSFER; LIGAND-BINDING; ALPHA-SUBUNIT;
D O I
10.2174/1568026611313010007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:64 / 77
页数:14
相关论文
共 217 条
[1]   Hydrophobic, hydrophilic, and charged amino acid networks within protein [J].
Aftabuddin, Md. ;
Kundu, S. .
BIOPHYSICAL JOURNAL, 2007, 93 (01) :225-231
[2]   Network analysis of protein structures identifies functional residues [J].
Amitai, G ;
Shemesh, A ;
Sitbon, E ;
Shklar, M ;
Netanely, D ;
Venger, I ;
Pietrokovski, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 344 (04) :1135-1146
[3]   Conserved amino acids participate in the structure networks deputed to intramolecular communication in the lutropin receptor [J].
Angelova, Krassimira ;
Felline, Angelo ;
Lee, Moon ;
Patel, Manish ;
Puett, David ;
Fanelli, Francesca .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (07) :1227-1239
[4]   Perturbation Waves in Proteins and Protein Networks: Applications of Percolation and Game Theories in Signaling and Drug Design [J].
Antal, Miklos A. ;
Csaba Boede ;
Csermely, Peter .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2009, 10 (02) :161-172
[5]  
Atilgan AR, 2007, BIOPHYS J, V92, P3052, DOI [10.1529/biophysj.106.099440, 10.1529/biophysj. 106.099440]
[6]   Small-world communication of residues and significance for protein dynamics [J].
Atilgan, AR ;
Akan, P ;
Baysal, C .
BIOPHYSICAL JOURNAL, 2004, 86 (01) :85-91
[7]   Perturbation-Response Scanning Reveals Ligand Entry-Exit Mechanisms of Ferric Binding Protein [J].
Atilgan, Canan ;
Atilgan, Ali Rana .
PLOS COMPUTATIONAL BIOLOGY, 2009, 5 (10)
[8]   The network as the target [J].
Baggs, Julie E. ;
Hughes, Michael E. ;
Hogenesch, John B. .
WILEY INTERDISCIPLINARY REVIEWS-SYSTEMS BIOLOGY AND MEDICINE, 2010, 2 (02) :127-133
[9]   Network properties of protein structures [J].
Bagler, G ;
Sinha, S .
PHYSICA A-STATISTICAL MECHANICS AND ITS APPLICATIONS, 2005, 346 (1-2) :27-33
[10]   Assortative mixing in Protein Contact Networks and protein folding kinetics [J].
Bagler, Ganesh ;
Sinha, Somdatta .
BIOINFORMATICS, 2007, 23 (14) :1760-1767