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小分子结合剂和非结合剂与FMN核糖开关的结合自由能景观:全原子分子动力学

Binding free-energy landscapes of small molecule binder and non-binder to FMN riboswitch: All-atom molecular dynamics.

作者信息

Higo Junichi, Bekker Gert-Jan, Kamiya Narutoshi, Fukuda Ikuo, Fukunishi Yoshifumi

机构信息

Graduate School of Information Science, University of Hyogo, Kobe, Hyogo 650-0047, Japan.

Research Organization of Science and Technology, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan.

出版信息

Biophys Physicobiol. 2023 Dec 13;20(4):e200047. doi: 10.2142/biophysico.bppb-v20.0047. eCollection 2023.

Abstract

A small and flexible molecule, ribocil A (non-binder) or B (binder), binds to the deep pocket of the aptamer domain of the FMN riboswitch, which is an RNA molecule. This binding was studied by mD-VcMD, which is a generalized-ensemble simulation method. Ribocil A and B are structurally similar because they are optical isomers to each other. In the initial conformation of simulation, the ligands and the aptamer were completely dissociated in explicit solvent. The aptamer-ribocil B binding was stronger than the aptamer-ribocil A binding, which agrees with experiments. The computed free-energy landscape for the aptamer-ribocil B binding was funnel-like, whereas that for the aptamer-ribocil A binding was rugged. When passing through the gate (named "front gate") of the binding pocket, each ligand interacted with bases of the riboswitch by non-native π-π stackings, and the stackings restrained the ligand's orientation to be advantageous to reach the binding site smoothly. When the ligands reached the binding site in the pocket, the non-native stackings were replaced by the native stackings. The ligand's orientation restriction is discussed referring to a selection mechanism reported in an earlier work on a drug-GPCR interaction. The present simulation showed another pathway leading the ligands to the binding site. The gate ("rear gate") for this pathway was located completely opposite to the front gate on the aptamer's surface. However, the approach from the rear gate required overcoming a free-energy barrier regarding ligand's rotation before reaching the binding site.

摘要

一种小的柔性分子,核黄素类似物A(非结合剂)或B(结合剂),与FMN核糖开关适体结构域的深口袋结合,该核糖开关是一种RNA分子。这种结合通过mD-VcMD进行研究,mD-VcMD是一种广义系综模拟方法。核黄素类似物A和B在结构上相似,因为它们彼此是旋光异构体。在模拟的初始构象中,配体和适体在显式溶剂中完全解离。适体与核黄素类似物B的结合比适体与核黄素类似物A的结合更强,这与实验结果一致。计算得到的适体与核黄素类似物B结合的自由能景观呈漏斗状,而适体与核黄素类似物A结合的自由能景观则崎岖不平。当穿过结合口袋的“前门”时,每个配体通过非天然的π-π堆积与核糖开关的碱基相互作用,这些堆积限制了配体的取向,有利于其顺利到达结合位点。当配体到达口袋中的结合位点时,非天然堆积被天然堆积所取代。参照早期关于药物与GPCR相互作用的一项研究中报道的选择机制,讨论了配体的取向限制。本模拟显示了另一条引导配体到达结合位点的途径。这条途径的“后门”与适体表面的前门完全相对。然而,从后门接近需要在到达结合位点之前克服关于配体旋转的自由能垒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06d/10853809/81dbfa8ce001/20_e200047-g001.jpg

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