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通过分子动力学模拟了解β2肾上腺素能受体中D130N突变对组成型激活和药物结合的影响。

Understanding the effects on constitutive activation and drug binding of a D130N mutation in the β2 adrenergic receptor via molecular dynamics simulation.

作者信息

Zhu Yanyan, Yuan Yuan, Xiao Xiuchan, Zhang Liyun, Guo Yanzhi, Pu Xuemei

机构信息

Faculty of Chemistry, Sichuan University, No. 29 Jiuyanqiao Wangjiang Road, Chengdu, 610064, People's Republic of China.

出版信息

J Mol Model. 2014 Nov;20(11):2491. doi: 10.1007/s00894-014-2491-2. Epub 2014 Oct 25.

Abstract

G-protein-coupled receptors (GPCRs) are currently one of the largest families of drug targets. The constitutive activation induced by mutation of key GPCR residues is associated closely with various diseases. However, the structural basis underlying such activation and its role in drug binding has remained unclear. Herein, we used all-atom molecular dynamics simulations and free energy calculations to study the effects of a D130N mutation on the structure of β2 adrenergic receptor (β2AR) and its binding of the agonist salbutamol. The results indicate that the mutation caused significant changes in some key helices. In particular, the mutation leads to the departure of transmembrane 3 (TM3) from transmembrane 6 (TM6) and marked changes in the NPxxY region as well as the complete disruption of a key ionic lock, all of which contribute to the observed constitutive activation. In addition, the D130N mutation weakens some important H-bonds, leading to structural changes in these regions. Binding free energy calculations indicate that van der Waals and electrostatic interactions are the main driving forces in binding salbutamol; however, binding strength in the mutant β2AR is significantly enhanced mainly through modifying electrostatic interactions. Further analysis revealed that the increase in binding energy upon mutation stems mainly from the H-bonds formed between the hydroxyl group of salbutamol and the serine residues of TM5. This observation suggests that modifications of the H-bond groups of this drug could significantly influence drug efficacy in the treatment of diseases associated with this mutation.

摘要

G蛋白偶联受体(GPCRs)是目前最大的药物靶点家族之一。由关键GPCR残基突变引起的组成性激活与多种疾病密切相关。然而,这种激活背后的结构基础及其在药物结合中的作用仍不清楚。在此,我们使用全原子分子动力学模拟和自由能计算来研究D130N突变对β2肾上腺素能受体(β2AR)结构及其激动剂沙丁胺醇结合的影响。结果表明,该突变导致一些关键螺旋发生显著变化。特别是,该突变导致跨膜3(TM3)与跨膜6(TM6)分离,NPxxY区域发生明显变化,以及一个关键离子锁完全破坏,所有这些都导致了观察到的组成性激活。此外,D130N突变削弱了一些重要的氢键,导致这些区域的结构变化。结合自由能计算表明,范德华力和静电相互作用是结合沙丁胺醇的主要驱动力;然而,突变型β2AR中的结合强度主要通过改变静电相互作用而显著增强。进一步分析表明,突变后结合能的增加主要源于沙丁胺醇羟基与TM5丝氨酸残基之间形成的氢键。这一观察结果表明,该药物氢键基团的修饰可能会显著影响与该突变相关疾病治疗中的药物疗效。

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