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阿片类镇痛药与μ阿片受体的差异相互作用模式与配体特异性电压敏感性相关。

Differential interaction patterns of opioid analgesics with µ opioid receptors correlate with ligand-specific voltage sensitivity.

机构信息

Department of Pharmacology and Clinical Pharmacy, University of Marburg, Marburg, Germany.

Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom.

出版信息

Elife. 2023 Nov 20;12:e91291. doi: 10.7554/eLife.91291.

Abstract

The µ opioid receptor (MOR) is the key target for analgesia, but the application of opioids is accompanied by several issues. There is a wide range of opioid analgesics, differing in their chemical structure and their properties of receptor activation and subsequent effects. A better understanding of ligand-receptor interactions and the resulting effects is important. Here, we calculated the respective binding poses for several opioids and analyzed interaction fingerprints between ligand and receptor. We further corroborated the interactions experimentally by cellular assays. As MOR was observed to display ligand-induced modulation of activity due to changes in membrane potential, we further analyzed the effects of voltage sensitivity on this receptor. Combining in silico and in vitro approaches, we defined discriminating interaction patterns responsible for ligand-specific voltage sensitivity and present new insights into their specific effects on activation of the MOR.

摘要

μ 阿片受体(MOR)是镇痛的关键靶点,但阿片类药物的应用伴随着一些问题。有广泛的阿片类镇痛药,它们在化学结构、受体激活特性和随后的作用方面存在差异。更好地了解配体-受体相互作用和由此产生的影响很重要。在这里,我们计算了几种阿片类药物的各自结合构象,并分析了配体与受体之间的相互作用指纹。我们进一步通过细胞测定实验验证了这些相互作用。由于 MOR 被观察到由于膜电位的变化而显示出配体诱导的活性调节,我们进一步分析了电压敏感性对该受体的影响。通过将计算和体外方法相结合,我们定义了区分相互作用模式,这些模式负责配体特异性电压敏感性,并提供了对其对 MOR 激活的具体影响的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7273/10849675/09efb708cfa6/elife-91291-fig1.jpg

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