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Calculation of Standard Binding Free Energies:  Aromatic Molecules in the T4 Lysozyme L99A Mutant.标准结合自由能的计算:T4溶菌酶L99A突变体中的芳香族分子
J Chem Theory Comput. 2006 Sep;2(5):1255-73. doi: 10.1021/ct060037v.
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All-atom empirical potential for molecular modeling and dynamics studies of proteins.蛋白质分子建模和动力学研究的全原子经验势。
J Phys Chem B. 1998 Apr 30;102(18):3586-616. doi: 10.1021/jp973084f.
3
The different flexibility of c-Src and c-Abl kinases regulates the accessibility of a druggable inactive conformation.不同的 c-Src 和 c-Abl 激酶的灵活性调节了可成药的无活性构象的可及性。
J Am Chem Soc. 2012 Feb 8;134(5):2496-9. doi: 10.1021/ja210751t. Epub 2012 Jan 30.
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Binding free energy calculation with QM/MM hybrid methods for Abl-Kinase inhibitor.使用量子力学/分子力学混合方法对Abl激酶抑制剂进行结合自由能计算。
J Biol Phys. 2011 Jan;37(1):69-78. doi: 10.1007/s10867-010-9199-z. Epub 2010 Sep 2.
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Free Energy Perturbation Hamiltonian Replica-Exchange Molecular Dynamics (FEP/H-REMD) for Absolute Ligand Binding Free Energy Calculations.用于绝对配体结合自由能计算的自由能微扰哈密顿量副本交换分子动力学(FEP/H-REMD)
J Chem Theory Comput. 2010 Jul 1;6(9):2559-2565. doi: 10.1021/ct1001768.
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Computation of Absolute Hydration and Binding Free Energy with Free Energy Perturbation Distributed Replica-Exchange Molecular Dynamics (FEP/REMD).基于自由能微扰分布式复制交换分子动力学(FEP/REMD)的绝对水合和结合自由能计算
J Chem Theory Comput. 2009 Oct 1;5(10):2583-2588. doi: 10.1021/ct900223z.
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How does a drug molecule find its target binding site?药物分子如何找到其靶标结合位点?
J Am Chem Soc. 2011 Jun 22;133(24):9181-3. doi: 10.1021/ja202726y. Epub 2011 May 13.
8
Resistance to imatinib: mutations and beyond.伊马替尼耐药:突变及其他。
Semin Hematol. 2010 Oct;47(4):335-43. doi: 10.1053/j.seminhematol.2010.06.005.
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Absolute binding free energy calculations of sparsomycin analogs to the bacterial ribosome.疏螺旋体素类似物与细菌核糖体的绝对结合自由能计算。
J Phys Chem B. 2010 Jul 29;114(29):9525-39. doi: 10.1021/jp100579y.
10
Analysis of imatinib and sorafenib binding to p38alpha compared with c-Abl and b-Raf provides structural insights for understanding the selectivity of inhibitors targeting the DFG-out form of protein kinases.分析伊马替尼和索拉非尼与 p38α 的结合情况,并与 c-Abl 和 b-Raf 进行比较,为理解针对蛋白激酶 DFG-out 构象的抑制剂的选择性提供了结构见解。
Biochemistry. 2010 May 4;49(17):3611-8. doi: 10.1021/bi100070r.

解释为什么格列卫是 Abl 激酶的一种特异性和强效抑制剂。

Explaining why Gleevec is a specific and potent inhibitor of Abl kinase.

机构信息

Department of Biochemistry and Molecular Biology, Gordon Center for Integrative Science, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Jan 29;110(5):1664-9. doi: 10.1073/pnas.1214330110. Epub 2013 Jan 14.

DOI:10.1073/pnas.1214330110
PMID:23319661
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3562763/
Abstract

Tyrosine kinases present attractive drug targets for specific types of cancers. Gleevec, a well-known therapeutic agent against chronic myelogenous leukemia, is an effective inhibitor of Abl tyrosine kinase. However, Gleevec fails to inhibit closely homologous tyrosine kinases, such as c-Src. Because many structural features of the binding site are conserved, the molecular determinants responsible for binding specificity are not immediately apparent. Some have attributed the difference in binding specificity of Gleevec to subtle variations in ligand-protein interactions (binding affinity control), whereas others have proposed that it is the conformation of the DFG motif, in which ligand binding is only accessible to Abl and not to c-Src (conformational selection control). To address this issue, the absolute binding free energy was computed using all-atom molecular dynamics simulations with explicit solvent. The results of the free energy simulations are in good agreement with experiments, thereby enabling a meaningful decomposition of the binding free energy to elucidate the factors controlling Gleevec's binding specificity. The latter is shown to be controlled by a conformational selection mechanism and also by differences in key van der Waals interactions responsible for the stabilization of Gleevec in the binding pocket of Abl.

摘要

酪氨酸激酶是一类有吸引力的药物靶点,适用于某些类型的癌症。格列卫(Gleevec)是一种治疗慢性髓性白血病的知名药物,它是 Abl 酪氨酸激酶的有效抑制剂。然而,格列卫无法抑制密切相关的酪氨酸激酶,如 c-Src。由于结合位点的许多结构特征是保守的,负责结合特异性的分子决定因素并不明显。有人将格列卫结合特异性的差异归因于配体-蛋白相互作用(结合亲和力控制)中的细微变化,而另一些人则提出,它是 DFG 基序的构象,配体结合仅对 Abl 而不是 c-Src 是可及的(构象选择控制)。为了解决这个问题,使用包含显式溶剂的全原子分子动力学模拟来计算绝对结合自由能。自由能模拟的结果与实验非常吻合,从而能够对结合自由能进行有意义的分解,以阐明控制格列卫结合特异性的因素。结果表明,后者受构象选择机制和负责稳定格列卫在 Abl 结合口袋中的关键范德华相互作用的差异控制。