Maccari Giorgio, Mori Mattia, Rodríguez-Salarichs Javier, Fang Weishuo, Díaz José Fernando, Botta Maurizio
Dipartimento Farmaco-Chimico Tecnologico, Facoltà di Farmacia, Università degli Studi di Siena , I-53100 Siena, Italy.
Dipartimento di Chimica e Tecnologia del Farmaco, Università di Roma "La Sapienza" , I-00185 Roma, Italy.
J Chem Theory Comput. 2013 Jan 8;9(1):698-706. doi: 10.1021/ct3006612. Epub 2012 Nov 16.
Several pieces of experimental evidence led us to hypothesize that the mechanism of action of paclitaxel (Taxol) could involve a two-steps binding process, with paclitaxel first binding within the outer wall of microtubules and then moving into the inner binding site. In this work, we first used multiply targeted molecular dynamics (MTMD) for steering paclitaxel from the outer toward the inner binding site. This rough trajectory was then submitted to a refinement procedure in the path collective variables space. Paclitaxel binding energy was monitored along the refined pathway, highlighting the relevance of residues belonging to the H6-H7 and the M- loops. Computational results were supported by kinetics studies performed on fluorescent paclitaxel derivatives.
多项实验证据使我们推测紫杉醇(泰素)的作用机制可能涉及两步结合过程,即紫杉醇首先结合在微管外壁内,然后移动到内部结合位点。在这项工作中,我们首先使用多靶点分子动力学(MTMD)将紫杉醇从外部导向内部结合位点。然后将这个粗略的轨迹提交到路径集体变量空间中的优化程序。沿着优化后的路径监测紫杉醇的结合能,突出了属于H6-H7和M环的残基的相关性。荧光紫杉醇衍生物的动力学研究支持了计算结果。