Structural insight into the mechanism of epothilone A bound to beta-tubulin and its mutants at Arg282Gln and Thr274Ile
文献类型：期刊论文
| 作者 | Shi, Guojun1; Wang, Yue1; Jin, Yi1; Chi, Shaoming1; Shi, Qiang2; Ge, Maofa2; Wang, Shu3; Zhang, Xingkang2; Xu, Sichuan1 |
| 刊名 | JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
 |
| 出版日期 | 2012 |
| 卷号 | 30期号:5页码:559-573 |
| 关键词 | Epoa Taxol Tubulin Active Pocket Mechanism Md Simulation Dft |
| ISSN号 | 0739-1102 |
| DOI | 10.1080/07391102.2012.687522 |
| 英文摘要 | Epothilone A (EpoA) is under investigation as an antitumor agent. To provide better understanding of the activity of EpoA against cancers, by theoretical studies such as using docking method, molecular dynamics simulation and density functional theory calculations, we identify several key residues located on beta-tubulin as the active sites to establish an active pocket responsible for interaction with EpoA. Eight residues (Arg276, Asp224, Asp26, His227, Glu27, Glu22, Thr274, and Met363) are identified as the active sites to form the active pocket on beta-tubulin. The interaction energy is predicted to be -121.3 kJ/mol between EpoA and beta-tubulin. In the mutant of beta-tubulin at Thr274Ile, three residues (Arg359, Glu27, and His227) are identified as the active sites for the binding of EpoA. In the mutant of beta-tubulin at Arg282Gln, three residues (Arg276, Lys19, and His227) serve as the active sites. The interaction energy is reduced to -77.2 kJ/mol between EpoA and Arg282Gln mutant and to -50.2 kJ/mol between EpoA and Thr274Ile mutant. The strong interaction with beta-tubulin is significant to EpoA's activity against cancer cells. When beta-tubulin is mutated either at Arg282Gln or at Thr274Ile, the decreased strength of interaction explains the activity reduced for EpoA. Therefore, this work shows that the structural basis of the active pocket plays an important role in regulating the activity for EpoA with a Taxol-like mechanism of action to be promoted as an antitumor agent. |
| 语种 | 英语 |
| WOS记录号 | WOS:000308104500006 |
| 出版者 | TAYLOR & FRANCIS INC |
| 源URL | [http://ir.iccas.ac.cn/handle/121111/47675]  |
| 专题 | 中国科学院化学研究所 |
| 通讯作者 | Xu, Sichuan |
| 作者单位 | 1.Yunnan Univ, Coll Chem Sci & Technol, Key Lab, Educ Minist Med Chem Nat Resource, Kunming 650091, Peoples R China 2.Chinese Acad Sci, State Key Lab Struct Chem Unstable & Stable Speci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100080, Peoples R China 3.Chinese Acad Sci, CAS Key Lab Organ Solids, Inst Chem, Beijing 100080, Peoples R China |
| 推荐引用方式 GB/T 7714 | Shi, Guojun,Wang, Yue,Jin, Yi,et al. Structural insight into the mechanism of epothilone A bound to beta-tubulin and its mutants at Arg282Gln and Thr274Ile[J]. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS,2012,30(5):559-573. |
| APA | Shi, Guojun.,Wang, Yue.,Jin, Yi.,Chi, Shaoming.,Shi, Qiang.,...&Xu, Sichuan.(2012).Structural insight into the mechanism of epothilone A bound to beta-tubulin and its mutants at Arg282Gln and Thr274Ile.JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS,30(5),559-573. |
| MLA | Shi, Guojun,et al."Structural insight into the mechanism of epothilone A bound to beta-tubulin and its mutants at Arg282Gln and Thr274Ile".JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 30.5(2012):559-573. |
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来源：化学研究所
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