Suppr超能文献

核受体RORγ中蛋白质-配体相互作用模式的统计分析

Statistical Analysis of Protein-Ligand Interaction Patterns in Nuclear Receptor RORγ.

作者信息

Pham Bill, Cheng Ziju, Lopez Daniel, Lindsay Richard J, Foutch David, Majors Rily T, Shen Tongye

机构信息

Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN, United States.

UT-ORNL Graduate School of Genome Science and Technology, Knoxville, TN, United States.

出版信息

Front Mol Biosci. 2022 Jun 15;9:904445. doi: 10.3389/fmolb.2022.904445. eCollection 2022.

Abstract

The receptor RORγ belongs to the nuclear receptor superfamily that senses small signaling molecules and regulates at the gene transcription level. Since RORγ has a high basal activity and plays an important role in immune responses, inhibitors targeting this receptor have been a focus for many studies. The receptor-ligand interaction is complex, and often subtle differences in ligand structure can determine its role as an inverse agonist or an agonist. We examined more than 130 existing RORγ crystal structures that have the same receptor complexed with different ligands. We reported the features of receptor-ligand interaction patterns and the differences between agonist and inverse agonist binding. Specific changes in the contact interaction map are identified to distinguish active and inactive conformations. Further statistical analysis of the contact interaction patterns using principal component analysis reveals a dominant mode which separates allosteric binding vs. canonical binding and a second mode which may indicate active vs. inactive structures. We also studied the nature of constitutive activity by performing a 100-ns computer simulation of apo RORγ. Using constitutively active nuclear receptor CAR as a comparison, we identified a group of conserved contacts that have similar contact strength between the two receptors. These conserved contact interactions, especially a couple key contacts in H11-H12 interaction, can be considered essential to the constitutive activity of RORγ. These protein-ligand and internal protein contact interactions can be useful in the development of new drugs that direct receptor activity.

摘要

受体RORγ属于核受体超家族,该家族可感知小分子信号分子并在基因转录水平进行调控。由于RORγ具有较高的基础活性且在免疫反应中发挥重要作用,针对该受体的抑制剂一直是众多研究的焦点。受体与配体的相互作用较为复杂,配体结构上往往细微的差异就能决定其作为反向激动剂或激动剂的作用。我们研究了130多个现有的RORγ晶体结构,这些结构中受体相同但结合了不同的配体。我们报道了受体-配体相互作用模式的特征以及激动剂和反向激动剂结合之间的差异。通过识别接触相互作用图谱中的特定变化来区分活性和非活性构象。使用主成分分析对接触相互作用模式进行进一步的统计分析,揭示了一种区分变构结合与典型结合的主导模式以及另一种可能指示活性与非活性结构的模式。我们还通过对无配体RORγ进行100纳秒的计算机模拟研究了组成型活性的本质。以组成型活性核受体CAR作为对照,我们确定了一组在两个受体之间具有相似接触强度的保守接触。这些保守的接触相互作用,尤其是H11-H12相互作用中的几个关键接触,可以被认为是RORγ组成型活性所必需的。这些蛋白质-配体和蛋白质内部的接触相互作用可能有助于开发直接调控受体活性的新药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/467c/9240913/24f13dda1a05/fmolb-09-904445-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验