丝氨酸 3.39 和异亮氨酸 4.60 是 5-HT2AR 介导的 Gs 信号转导的关键位点。

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology FEBS Letters Pub Date : 2024-05-16 DOI:10.1002/1873-3468.14904
Lulu Xie, Xiaoqian Liu, Yishan Yao, Bo Tan, Ruibin Su
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引用次数: 0

摘要

5-HT2AR 的某些氨基酸位点在与各种 G 蛋白相互作用方面发挥着关键作用。致幻剂和非致幻剂都作用于 5-HT2AR 但却产生不同的药理作用,这可能是由于不同 G 蛋白的耦合作用。因此,本研究通过分子对接确定了致幻剂和非致幻剂与 5-HT2AR 的结合位点。我们通过位点突变来研究这些位点对G蛋白的影响,从而找出能够区分致幻剂和非致幻剂药理作用的位点。我们的结果表明,I4.60A 和 S3.39A 不影响致幻剂激活 Gq 信号的能力,但却显著降低了致幻剂激活 Gs 信号的能力。这些结果表明,S3.39 和 I4.60 对致幻剂激活 Gs 信号非常重要。
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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Serine 3.39 and isoleucine 4.60 are key sites for 5-HT2AR-mediated Gs signaling

Certain amino acid sites of 5-HT2AR play crucial roles in interacting with various G proteins. Hallucinogens and non-hallucinogens both act on 5-HT2AR but mediate different pharmacological effects, possibly due to the coupling of different G proteins. Therefore, this study identified the binding sites of hallucinogens and non-hallucinogens with 5-HT2AR through molecular docking. We conducted site mutation to examine the impact of these sites on G proteins, in order to find out the sites that can distinguish the pharmacological effects of hallucinogens and non-hallucinogens. Our results indicate that I4.60A and S3.39A did not affect the ability of hallucinogens to activate Gq signaling, but significantly reduced Gs signaling activation by hallucinogens. These results suggest that S3.39 and I4.60 are important for the activation of Gs signaling by hallucinogens.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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