Binding of ligands to the aryl hydrocarbon receptor: An overview of methods.

IF 2.9 3区 医学 Q2 TOXICOLOGY Toxicology letters Pub Date : 2025-01-18 DOI:10.1016/j.toxlet.2025.01.003
Jiří Hrubý, Zdeněk Dvořák
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Abstract

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor, which plays numerous and pivotal roles in human physiology and pathophysiology. Therefore, pharmacotherapeutic targeting of the AhR is a highly pertinent issue. The identification of new AhR ligands and the characterization of the interactions between the AhR ligands and AhR protein requires appropriate methodology. In spite the AhR is monomeric intracellular soluble receptor, the full-length human AhR protein has not been crystallized so far, and its isolation in a form applicable in the binding assays is highly challenging. Recent advances, including crystallization of AhR fragments, recombinant protein technologies, and cryogenic electron microscopy, allowed for exploitation of diverse experimental techniques for studying interactions between ligands and the AhR. In the current paper, we review existing AhR ligand binding assays, including their description, applicability and limitations.

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配体与芳烃受体的结合:方法综述。
芳烃受体(aryl hydrocarbon receptor, AhR)是一种配体激活的转录因子,在人体生理和病理生理中起着重要的作用。因此,AhR的药物治疗靶向性是一个高度相关的问题。鉴定新的AhR配体以及表征AhR配体与AhR蛋白之间的相互作用需要适当的方法。尽管AhR是细胞内可溶的单体受体,但全长人AhR蛋白迄今尚未结晶,并且其以适用于结合测定的形式分离是极具挑战性的。最近的进展,包括AhR片段的结晶,重组蛋白技术和低温电子显微镜,允许利用不同的实验技术来研究配体和AhR之间的相互作用。在本文中,我们回顾了现有的AhR配体结合分析,包括它们的描述,适用性和局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Toxicology letters
Toxicology letters 医学-毒理学
CiteScore
7.10
自引率
2.90%
发文量
897
审稿时长
33 days
期刊介绍: An international journal for the rapid publication of novel reports on a range of aspects of toxicology, especially mechanisms of toxicity.
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