McFerrin Katherine G, Pang Yuan-Ping
Computer-Aided Molecular Design Laboratory, Mayo Clinic, Rochester, MN, USA.
Commun Chem. 2021 Mar 1;4(1):26. doi: 10.1038/s42004-021-00469-3.
Molecular dynamics simulations of hemicarcerands and related variants allow the study of constrictive binding and offer insight into the rules of molecular complexation, but are limited because three-dimensional models of hemicarcerands are tedious to build and their atomic charges are complicated to derive. There have been no molecular dynamics simulations of the reported water-soluble hemicarcerand (Octacid4) that explain how Octacid4 encapsulates guests at 298 K and keeps them encapsulated at 298 K in NMR experiments. Herein we report a modular approach to hemicarcerand simulations that simplifies the model building and charge derivation in a manner reminiscent of the approach to protein simulations with truncated amino acids as building blocks. We also report that in aqueous molecular dynamics simulations at 298 K apo Octacid4 adopts two clusters of conformations one of which has an equatorial portal open but the guest-bound Octacid4 adopts one cluster of conformations with all portals closed. These results explain how Octacid4 incarcerates guests at room temperature and suggest that the guest-induced host conformational change that impedes decomplexation is a previously unrecognized conformational characteristic that promotes strong molecular complexation.
半穴醚及其相关变体的分子动力学模拟有助于研究收缩性结合,并深入了解分子络合的规则,但存在局限性,因为半穴醚的三维模型构建繁琐,其原子电荷推导复杂。目前尚未有针对已报道的水溶性半穴醚(Octacid4)的分子动力学模拟,以解释Octacid4在298K时如何包封客体并在核磁共振实验中于298K保持包封状态。在此,我们报告一种用于半穴醚模拟的模块化方法,该方法以类似于使用截短氨基酸作为构建模块进行蛋白质模拟的方式简化了模型构建和电荷推导。我们还报告,在298K的水性分子动力学模拟中,脱辅基Octacid4呈现出两组构象簇,其中一组赤道门户开放,而结合客体的Octacid4则呈现出一组所有门户均关闭的构象簇。这些结果解释了Octacid4在室温下如何囚禁客体,并表明阻碍解络合的客体诱导主体构象变化是一种先前未被认识到的促进强分子络合的构象特征。