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G蛋白偶联受体旁系同源物对非同源内源性肽进行特异性识别的进化情景。

Evolutionary scenarios for the specific recognition of nonhomologous endogenous peptides by G protein-coupled receptor paralogs.

作者信息

Shiraishi Akira, Wada Azumi, Satake Honoo

机构信息

Bioorganic Research Institute, Suntory Foundation for Life Sciences, Kyoto, Japan.

Bioorganic Research Institute, Suntory Foundation for Life Sciences, Kyoto, Japan.

出版信息

J Biol Chem. 2025 Feb;301(2):108125. doi: 10.1016/j.jbc.2024.108125. Epub 2024 Dec 25.

Abstract

Several peptides interact with phylogenetically unrelated G protein-coupled receptors (GPCRs); similarly, orthologous GPCRs interact with distinct ligands. The neuropeptide substance P (SP) activates both NK1R and another unrelated primate-specific GPCR, MRGPRX2. Furthermore, MRGPRX1, a paralog of MRGPRX2, recognizes BAM8-22 (bovine adrenal medulla peptide 8-22), which has no evolutionary relatedness to SP. To elucidate the molecular basis and evolutionary history of this phylogenetically unrelated ligand selectivity, we developed a systematic procedure, the "interaction determinant likelihood score" system, which estimates the amino acid residues responsible for peptide-GPCR interactions predicted by peptide descriptor-incorporated support vector machine, our original machine learning-based peptide-GPCR interaction predictor. An interaction determinant likelihood score-based approach followed by pharmacological validation revealed the determinant residues for the ligand selectivity of SP-MRGPRX2 (F3.24 and G4.61) and BAM8-22-MRGPRX1 (L1.35). Molecular phylogenetic analysis revealed that the MRGPRX1 of common ancestral primates recognized BAM8-22, whereas the ancestral Cercopithecinae MRGPRX1 lost its interaction with BAM8-22 because of the loss of L1.35. The SP-MRGPRX2 interaction emerged in the common ancestors of Euarchonta, and, thereafter, the interaction of MRGPRX2 with both SP and BAM8-22 was acquired via substitution with L1.35 in several lineages. Collectively, the present study unraveled the molecular mechanisms and evolution of ligand specificity in evolutionary unrelated GPCRs.

摘要

几种肽与系统发育上不相关的G蛋白偶联受体(GPCR)相互作用;同样,直系同源GPCR与不同的配体相互作用。神经肽P物质(SP)可激活NK1R和另一种不相关的灵长类动物特异性GPCR,即MRGPRX2。此外,MRGPRX2的旁系同源物MRGPRX1可识别BAM8-22(牛肾上腺髓质肽8-22),它与SP没有进化相关性。为了阐明这种系统发育上不相关的配体选择性的分子基础和进化历史,我们开发了一种系统程序,即“相互作用决定因素似然评分”系统,该系统可估计由结合肽描述符的支持向量机预测的肽与GPCR相互作用的氨基酸残基,这是我们基于机器学习的原始肽-GPCR相互作用预测器。基于相互作用决定因素似然评分的方法,随后进行药理学验证,揭示了SP-MRGPRX2(F3.24和G4.61)和BAM8-22-MRGPRX1(L1.35)配体选择性的决定残基。分子系统发育分析表明,共同祖先灵长类动物的MRGPRX1可识别BAM8-22,而祖先猕猴亚目MRGPRX1由于L1.35的缺失而失去了与BAM8-22的相互作用。SP-MRGPRX2相互作用出现在真灵长大目(Euarchonta)的共同祖先中,此后,MRGPRX2与SP和BAM8-22的相互作用通过在几个谱系中用L1.35替代而获得。总体而言,本研究揭示了进化上不相关的GPCR中配体特异性的分子机制和进化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cb2/11910321/579163f3a969/gr1.jpg

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