中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
STUDY ON THE INTERACTIONS OF Smac MIMETICS WITH XIAP-BIR3 DOMAIN BY DOCKING AND MOLECULAR DYNAMICS SIMULATIONS

文献类型:期刊论文

作者Ling, Baoping1; Zhang, Rui2; Wang, Zhiguo2; Liu, Yongjun1,2; Liu, Chengbu1
刊名JOURNAL OF THEORETICAL & COMPUTATIONAL CHEMISTRY
出版日期2010-08-01
卷号9期号:4页码:797-812
关键词Inhibitor Of Apoptosis Protein (Iap) Smac Mimetics Molecular Docking Molecular Dynamics Simulations Binding Free Energy
ISSN号0219-6336
文献子类Article
英文摘要Upon receiving an apoptotic stimulus, the mature mitochondrial protein second mitochondria-derived activator of caspases (Smac)direct IAP-binding protein with low PI (DIABLO), which could be released from mitochondria into the cytosol together with cytochrome C, specifically binds to inhibitor of apoptosis proteins (IAPs) and relieves the inhibitory effect of caspase, thus promotes cell death. Some artificial small molecules (called Smac mimetics) can mimic the N-terminal four residues Ala1-Val2-Pro3-Ile4 (AVPI) sequence of mitochondrial protein Smac, and competitively bind to X-linked inhibitor of apoptosis protein baculoviral IAP repeats (XIAP-BIR3) domain with caspase-9, which leads to the removal of the inhibition of caspase-9 by XIAP and induce apoptosis. To gain an insight into the nature of XIAP-BIR3 domain recognizing Smac mimetics, we used docking and molecular dynamics simulations methods to study four representative Smac mimetics. The docking results show that the orientations of these backbones of ligands are identical with that of AVPI in the binding pocket. Each ligand corresponds to two competitive conformations, which are called extended and bended conformations. The results of molecular dynamics simulations show that the extended conformation is more stable, and the calculations of energy decomposition reveal that the residue Thr308 makes the strongest interaction with XIAP-BIR3. In addition, Asp309, Glu314, and Trp323 are indispensable for XIAP-BIR3 recognizing and binding Smac mimetics.; Upon receiving an apoptotic stimulus, the mature mitochondrial protein second mitochondria-derived activator of caspases (Smac)direct IAP-binding protein with low PI (DIABLO), which could be released from mitochondria into the cytosol together with cytochrome C, specifically binds to inhibitor of apoptosis proteins (IAPs) and relieves the inhibitory effect of caspase, thus promotes cell death. Some artificial small molecules (called Smac mimetics) can mimic the N-terminal four residues Ala1-Val2-Pro3-Ile4 (AVPI) sequence of mitochondrial protein Smac, and competitively bind to X-linked inhibitor of apoptosis protein baculoviral IAP repeats (XIAP-BIR3) domain with caspase-9, which leads to the removal of the inhibition of caspase-9 by XIAP and induce apoptosis. To gain an insight into the nature of XIAP-BIR3 domain recognizing Smac mimetics, we used docking and molecular dynamics simulations methods to study four representative Smac mimetics. The docking results show that the orientations of these backbones of ligands are identical with that of AVPI in the binding pocket. Each ligand corresponds to two competitive conformations, which are called extended and bended conformations. The results of molecular dynamics simulations show that the extended conformation is more stable, and the calculations of energy decomposition reveal that the residue Thr308 makes the strongest interaction with XIAP-BIR3. In addition, Asp309, Glu314, and Trp323 are indispensable for XIAP-BIR3 recognizing and binding Smac mimetics.
WOS关键词X-LINKED INHIBITOR ; MITOCHONDRIA-DERIVED ACTIVATOR ; STRUCTURE-BASED DESIGN ; APOPTOSIS PROTEIN XIAP ; PROGRAMMED CELL-DEATH ; BINDING FREE-ENERGY ; STRUCTURAL BASIS ; CASPASE ACTIVATION ; AUTOMATED DOCKING ; BIR3 DOMAIN
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000282444600008
公开日期2011-12-13
源URL[http://ir.nwipb.ac.cn//handle/363003/1658]  
专题西北高原生物研究所_中国科学院西北高原生物研究所
作者单位1.Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Shandong, Peoples R China
2.Chinese Acad Sci, NW Inst Plateau Biol, Xining 810001, Qinghai, Peoples R China
推荐引用方式
GB/T 7714
Ling, Baoping,Zhang, Rui,Wang, Zhiguo,et al. STUDY ON THE INTERACTIONS OF Smac MIMETICS WITH XIAP-BIR3 DOMAIN BY DOCKING AND MOLECULAR DYNAMICS SIMULATIONS[J]. JOURNAL OF THEORETICAL & COMPUTATIONAL CHEMISTRY,2010,9(4):797-812.
APA Ling, Baoping,Zhang, Rui,Wang, Zhiguo,Liu, Yongjun,&Liu, Chengbu.(2010).STUDY ON THE INTERACTIONS OF Smac MIMETICS WITH XIAP-BIR3 DOMAIN BY DOCKING AND MOLECULAR DYNAMICS SIMULATIONS.JOURNAL OF THEORETICAL & COMPUTATIONAL CHEMISTRY,9(4),797-812.
MLA Ling, Baoping,et al."STUDY ON THE INTERACTIONS OF Smac MIMETICS WITH XIAP-BIR3 DOMAIN BY DOCKING AND MOLECULAR DYNAMICS SIMULATIONS".JOURNAL OF THEORETICAL & COMPUTATIONAL CHEMISTRY 9.4(2010):797-812.

入库方式: OAI收割

来源:西北高原生物研究所

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