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丙氨酸扫描诱变人黑素皮质素受体 4 的 DRYxxI 基序和细胞内环 2。

Alanine Scanning Mutagenesis of the DRYxxI Motif and Intracellular Loop 2 of Human Melanocortin-4 Receptor.

机构信息

Department of Anatomy, Physiology and Pharmacology, Auburn University College of Veterinary Medicine, Auburn, AL 36849, USA.

出版信息

Int J Mol Sci. 2020 Oct 15;21(20):7611. doi: 10.3390/ijms21207611.

Abstract

The melanocortin-4 receptor (MC4R) is a member of the G-protein-coupled receptor (GPCR) superfamily, which has been extensively studied in obesity pathogenesis due to its critical role in regulating energy homeostasis. Both the Gs-cAMP and ERK1/2 cascades are known as important intracellular signaling pathways initiated by the MC4R. The DRYxxI motif at the end of transmembrane domain 3 and the intracellular loop 2 (ICL2) are thought to be crucial for receptor function in several GPCRs. To study the functions of this domain in MC4R, we performed alanine-scanning mutagenesis on seventeen residues. We showed that one residue was critical for receptor cell surface expression. Eight residues were important for ligand binding. Mutations of three residues impaired Gs-cAMP signaling without changing the binding properties. Investigation on constitutive activities of all the mutants in the cAMP pathway revealed that six residues were involved in constraining the receptor in inactive states and five residues were important for receptor activation in the absence of an agonist. In addition, mutations of four residues impaired the ligand-stimulated ERK1/2 signaling pathway without affecting the binding properties. We also showed that some mutants were biased to the Gs-cAMP or ERK1/2 signaling pathway. In summary, we demonstrated that the DRYxxI motif and ICL2 were important for MC4R function.

摘要

黑素皮质素-4 受体(MC4R)是 G 蛋白偶联受体(GPCR)超家族的成员,由于其在调节能量平衡中的关键作用,它在肥胖发病机制的研究中得到了广泛的研究。Gs-cAMP 和 ERK1/2 级联反应被认为是由 MC4R 启动的重要细胞内信号通路。跨膜域 3 末端的 DRYxxI 基序和细胞内环 2(ICL2)被认为是几种 GPCR 中受体功能的关键。为了研究该结构域在 MC4R 中的功能,我们对十七个残基进行了丙氨酸扫描诱变。结果表明,一个残基对于受体的细胞表面表达至关重要。八个残基对于配体结合很重要。三个残基的突变会损害 Gs-cAMP 信号转导,但不改变结合特性。对所有突变体在 cAMP 通路中的组成活性的研究表明,有六个残基参与约束受体处于非活性状态,五个残基对于无激动剂时受体的激活很重要。此外,四个残基的突变会损害配体刺激的 ERK1/2 信号通路,但不影响结合特性。我们还表明,一些突变体偏向于 Gs-cAMP 或 ERK1/2 信号通路。总之,我们证明了 DRYxxI 基序和 ICL2 对于 MC4R 功能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4633/7589821/f9ca93575f90/ijms-21-07611-g001.jpg

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