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Structural basis of CMKLR1 signaling induced by chemerin9
Chemokine-like receptor 1 (CMKLR1), also known as chemerin receptor 23 (ChemR23) or chemerin receptor 1, is a chemoattractant G protein-coupled receptor (GPCR) that responds to the adipokine chemerin and is highly expressed in innate immune cells, including macrophages and neutrophils. The signaling...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274904/ https://www.ncbi.nlm.nih.gov/pubmed/37333145 http://dx.doi.org/10.1101/2023.06.09.544295 |
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author | Zhang, Xuan Weiß, Tina Cheng, Mary Hongying Chen, Siqi Ambrosius, Carla Katharina Czerniak, Anne Sophie Li, Kunpeng Feng, Mingye Bahar, Ivet Beck-Sickinger, Annette G. Zhang, Cheng |
author_facet | Zhang, Xuan Weiß, Tina Cheng, Mary Hongying Chen, Siqi Ambrosius, Carla Katharina Czerniak, Anne Sophie Li, Kunpeng Feng, Mingye Bahar, Ivet Beck-Sickinger, Annette G. Zhang, Cheng |
author_sort | Zhang, Xuan |
collection | PubMed |
description | Chemokine-like receptor 1 (CMKLR1), also known as chemerin receptor 23 (ChemR23) or chemerin receptor 1, is a chemoattractant G protein-coupled receptor (GPCR) that responds to the adipokine chemerin and is highly expressed in innate immune cells, including macrophages and neutrophils. The signaling pathways of CMKLR1 can lead to both pro- and anti-inflammatory effects depending on the ligands and physiological contexts. To understand the molecular mechanisms of CMKLR1 signaling, we determined a high-resolution cryo-electron microscopy (cryo-EM) structure of the CMKLR1-G(i) signaling complex with chemerin9, a nanopeptide agonist derived from chemerin, which induced complex phenotypic changes of macrophages in our assays. The cryo-EM structure, together with molecular dynamics simulations and mutagenesis studies, revealed the molecular basis of CMKLR1 signaling by elucidating the interactions at the ligand-binding pocket and the agonist-induced conformational changes. Our results are expected to facilitate the development of small molecule CMKLR1 agonists that mimic the action of chemerin9 to promote the resolution of inflammation. |
format | Online Article Text |
id | pubmed-10274904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102749042023-06-17 Structural basis of CMKLR1 signaling induced by chemerin9 Zhang, Xuan Weiß, Tina Cheng, Mary Hongying Chen, Siqi Ambrosius, Carla Katharina Czerniak, Anne Sophie Li, Kunpeng Feng, Mingye Bahar, Ivet Beck-Sickinger, Annette G. Zhang, Cheng bioRxiv Article Chemokine-like receptor 1 (CMKLR1), also known as chemerin receptor 23 (ChemR23) or chemerin receptor 1, is a chemoattractant G protein-coupled receptor (GPCR) that responds to the adipokine chemerin and is highly expressed in innate immune cells, including macrophages and neutrophils. The signaling pathways of CMKLR1 can lead to both pro- and anti-inflammatory effects depending on the ligands and physiological contexts. To understand the molecular mechanisms of CMKLR1 signaling, we determined a high-resolution cryo-electron microscopy (cryo-EM) structure of the CMKLR1-G(i) signaling complex with chemerin9, a nanopeptide agonist derived from chemerin, which induced complex phenotypic changes of macrophages in our assays. The cryo-EM structure, together with molecular dynamics simulations and mutagenesis studies, revealed the molecular basis of CMKLR1 signaling by elucidating the interactions at the ligand-binding pocket and the agonist-induced conformational changes. Our results are expected to facilitate the development of small molecule CMKLR1 agonists that mimic the action of chemerin9 to promote the resolution of inflammation. Cold Spring Harbor Laboratory 2023-06-10 /pmc/articles/PMC10274904/ /pubmed/37333145 http://dx.doi.org/10.1101/2023.06.09.544295 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Zhang, Xuan Weiß, Tina Cheng, Mary Hongying Chen, Siqi Ambrosius, Carla Katharina Czerniak, Anne Sophie Li, Kunpeng Feng, Mingye Bahar, Ivet Beck-Sickinger, Annette G. Zhang, Cheng Structural basis of CMKLR1 signaling induced by chemerin9 |
title | Structural basis of CMKLR1 signaling induced by chemerin9 |
title_full | Structural basis of CMKLR1 signaling induced by chemerin9 |
title_fullStr | Structural basis of CMKLR1 signaling induced by chemerin9 |
title_full_unstemmed | Structural basis of CMKLR1 signaling induced by chemerin9 |
title_short | Structural basis of CMKLR1 signaling induced by chemerin9 |
title_sort | structural basis of cmklr1 signaling induced by chemerin9 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274904/ https://www.ncbi.nlm.nih.gov/pubmed/37333145 http://dx.doi.org/10.1101/2023.06.09.544295 |
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