Bian Xiaoli, Dong Wangqing, Zhao Yang, Sun Rui, Kong Wanjun, Li Yiping
Department of Pharmacy, College of Medicine, Xi'an Jiaotong University, No. 76 Yanta west Road, Xi'an, 710061, People's Republic of China.
J Mol Model. 2014 Apr;20(4):2166. doi: 10.1007/s00894-014-2166-z. Epub 2014 Mar 16.
Activation of the phosphatidylinositol 3-kinase α (PI3Kα) is commonly observed in human cancer and is critical for tumor progression, which has made PI3Kα an attractive target for anticancer drug discovery. To systematically investigate the binding mode of A-66S, a new selective PI3Kα inhibitor for PI3Kα, molecular docking, molecular dynamics simulation and ensuing energetic analysis were performed. The binding free energy between PI3Kα and A-66S is -11.27 kcal•mol⁻¹ using MMPBSA method, while -14.67 kcal•mol⁻¹ using MMGBSA method, which is beneficial for the binding, and the van der Waals/hydrophobic and electrostatic interactions are critical for the binding. The conserved hydrophobic adenine region of PI3Kα made up of Met772, Pro778, Ile800, Tyr836, Ile848, Val850, Val851, Met922, Phe930 and Ile932 accommodates the flat 2-tert-butyl-4'-methyl-4,5'-bithiazol moiety of A-66S, and the NH of Val851 forms a hydrogen with the nitrogen atom embedded in the aminothiazole ring of A-66S. The (S)-pyrrolidine carboxamide urea moiety especially extends toward the region of the binding site wall (Ser854-Gln859) defined by the C-terminal lobe, and has three hydrogen-bond arms with the backbone of Ser854 and the side chain of Gln859. Notably the interaction between the non-conserved residue Gln859 and A-66S is responsible for the selectivity profile of A-66S. The binding mode of A-66S for PI3Kα presented in this study should aid in the design of a new highly selective PI3Kα inhibitor.
磷脂酰肌醇3激酶α(PI3Kα)的激活在人类癌症中普遍存在,且对肿瘤进展至关重要,这使得PI3Kα成为抗癌药物研发中一个有吸引力的靶点。为了系统研究新型PI3Kα选择性抑制剂A-66S的结合模式,进行了分子对接、分子动力学模拟及后续的能量分析。采用MMPBSA方法时,PI3Kα与A-66S之间的结合自由能为-11.27 kcal•mol⁻¹,而采用MMGBSA方法时为-14.67 kcal•mol⁻¹,这有利于二者的结合,范德华力/疏水作用和静电相互作用对结合至关重要。PI3Kα由Met772、Pro778、Ile800、Tyr836、Ile848、Val850、Val851、Met922、Phe930和Ile932组成的保守疏水腺嘌呤区域容纳了A-66S扁平的2-叔丁基-4'-甲基-4,5'-联噻唑部分,Val851的NH与A-66S氨基噻唑环中嵌入的氮原子形成氢键。(S)-吡咯烷甲酰胺脲部分尤其伸向由C末端叶定义的结合位点壁(Ser854-Gln⑧59)区域,并与Ser854主链和Gln859侧链有三个氢键臂。值得注意的是,非保守残基Gln859与A-66S之间的相互作用决定了A-66S的选择性特征。本研究中展示的A-66S与PI3Kα的结合模式应有助于设计新型高选择性PI3Kα抑制剂。