Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, SE-141 83, Sweden.
J Comput Chem. 2017 Jun 5;38(15):1147-1157. doi: 10.1002/jcc.24692. Epub 2017 Jan 19.
Locked nucleic acid (LNA), a modified nucleoside which contains a bridging group across the ribose ring, improves the stability of DNA/RNA duplexes significantly, and therefore is of interest in biotechnology and gene therapy applications. In this study, we investigate the free energy change between LNA and DNA nucleosides. The transformation requires the breaking of the bridging group across the ribose ring, a problematic transformation in free energy calculations. To address this, we have developed a 3-step (easy to implement) and a 1-step protocol (more efficient, but more complicated to setup), for single and dual topologies in classical molecular dynamics simulations, using the Bennett Acceptance Ratio method to calculate the free energy. We validate the approach on the solvation free energy difference for the nucleosides thymidine, cytosine, and 5-methyl-cytosine. © 2017 The Authors. Journal of Computational Chemistry Published by Wiley Periodicals, Inc.
锁核酸(LNA)是一种经过修饰的核苷,其在核糖环上具有桥连基团,可显著提高 DNA/RNA 双链体的稳定性,因此在生物技术和基因治疗应用中具有重要意义。在这项研究中,我们研究了 LNA 和 DNA 核苷之间的自由能变化。这种转化需要打破核糖环上的桥连基团,这在自由能计算中是一个有问题的转化。为了解决这个问题,我们开发了一种 3 步(易于实施)和 1 步(更有效,但设置更复杂)的方案,用于经典分子动力学模拟中的单拓扑和双拓扑,使用 Bennett 接受率方法来计算自由能。我们在核苷胸苷、胞嘧啶和 5-甲基胞嘧啶的溶剂化自由能差上验证了该方法。©2017 作者。John Wiley & Sons, Inc. 出版的《计算机化学杂志》