Ofer Zimmerman, Maxwell I Zimmerman, Saravanan Raju, Christopher A Nelson, John M Errico, Emily A Madden, Autumn C Holmes, Ahmed O Hassan, Laura A VanBlargan, Arthur S Kim, Lucas J Adams, Katherine Basore, Bradley M Whitener, Sathvik Palakurty, Hannah G Davis-Adams, Chengqun Sun, Theron Gilliland, James T Earnest, Hongming Ma, Gregory D Ebel, Christian Zmasek, Richard H Scheuermann, William B Klimstra, Daved H Fremont, Michael S Diamond
{"title":"α病毒受体MXRA8的脊椎动物类特异性结合模式。","authors":"Ofer Zimmerman, Maxwell I Zimmerman, Saravanan Raju, Christopher A Nelson, John M Errico, Emily A Madden, Autumn C Holmes, Ahmed O Hassan, Laura A VanBlargan, Arthur S Kim, Lucas J Adams, Katherine Basore, Bradley M Whitener, Sathvik Palakurty, Hannah G Davis-Adams, Chengqun Sun, Theron Gilliland, James T Earnest, Hongming Ma, Gregory D Ebel, Christian Zmasek, Richard H Scheuermann, William B Klimstra, Daved H Fremont, Michael S Diamond","doi":"10.1016/j.cell.2023.09.007","DOIUrl":null,"url":null,"abstract":"<p><p>MXRA8 is a receptor for chikungunya (CHIKV) and other arthritogenic alphaviruses with mammalian hosts. However, mammalian MXRA8 does not bind to alphaviruses that infect humans and have avian reservoirs. Here, we show that avian, but not mammalian, MXRA8 can act as a receptor for Sindbis, western equine encephalitis (WEEV), and related alphaviruses with avian reservoirs. Structural analysis of duck MXRA8 complexed with WEEV reveals an inverted binding mode compared with mammalian MXRA8 bound to CHIKV. Whereas both domains of mammalian MXRA8 bind CHIKV E1 and E2, only domain 1 of avian MXRA8 engages WEEV E1, and no appreciable contacts are made with WEEV E2. Using these results, we generated a chimeric avian-mammalian MXRA8 decoy-receptor that neutralizes infection of multiple alphaviruses from distinct antigenic groups in vitro and in vivo. Thus, different alphaviruses can bind MXRA8 encoded by different vertebrate classes with distinct engagement modes, which enables development of broad-spectrum inhibitors.</p>","PeriodicalId":9656,"journal":{"name":"Cell","volume":" ","pages":"4818-4833.e25"},"PeriodicalIF":45.5000,"publicationDate":"2023-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615782/pdf/","citationCount":"0","resultStr":"{\"title\":\"Vertebrate-class-specific binding modes of the alphavirus receptor MXRA8.\",\"authors\":\"Ofer Zimmerman, Maxwell I Zimmerman, Saravanan Raju, Christopher A Nelson, John M Errico, Emily A Madden, Autumn C Holmes, Ahmed O Hassan, Laura A VanBlargan, Arthur S Kim, Lucas J Adams, Katherine Basore, Bradley M Whitener, Sathvik Palakurty, Hannah G Davis-Adams, Chengqun Sun, Theron Gilliland, James T Earnest, Hongming Ma, Gregory D Ebel, Christian Zmasek, Richard H Scheuermann, William B Klimstra, Daved H Fremont, Michael S Diamond\",\"doi\":\"10.1016/j.cell.2023.09.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>MXRA8 is a receptor for chikungunya (CHIKV) and other arthritogenic alphaviruses with mammalian hosts. However, mammalian MXRA8 does not bind to alphaviruses that infect humans and have avian reservoirs. Here, we show that avian, but not mammalian, MXRA8 can act as a receptor for Sindbis, western equine encephalitis (WEEV), and related alphaviruses with avian reservoirs. Structural analysis of duck MXRA8 complexed with WEEV reveals an inverted binding mode compared with mammalian MXRA8 bound to CHIKV. Whereas both domains of mammalian MXRA8 bind CHIKV E1 and E2, only domain 1 of avian MXRA8 engages WEEV E1, and no appreciable contacts are made with WEEV E2. Using these results, we generated a chimeric avian-mammalian MXRA8 decoy-receptor that neutralizes infection of multiple alphaviruses from distinct antigenic groups in vitro and in vivo. Thus, different alphaviruses can bind MXRA8 encoded by different vertebrate classes with distinct engagement modes, which enables development of broad-spectrum inhibitors.</p>\",\"PeriodicalId\":9656,\"journal\":{\"name\":\"Cell\",\"volume\":\" \",\"pages\":\"4818-4833.e25\"},\"PeriodicalIF\":45.5000,\"publicationDate\":\"2023-10-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615782/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cell.2023.09.007\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/10/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cell.2023.09.007","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Vertebrate-class-specific binding modes of the alphavirus receptor MXRA8.
MXRA8 is a receptor for chikungunya (CHIKV) and other arthritogenic alphaviruses with mammalian hosts. However, mammalian MXRA8 does not bind to alphaviruses that infect humans and have avian reservoirs. Here, we show that avian, but not mammalian, MXRA8 can act as a receptor for Sindbis, western equine encephalitis (WEEV), and related alphaviruses with avian reservoirs. Structural analysis of duck MXRA8 complexed with WEEV reveals an inverted binding mode compared with mammalian MXRA8 bound to CHIKV. Whereas both domains of mammalian MXRA8 bind CHIKV E1 and E2, only domain 1 of avian MXRA8 engages WEEV E1, and no appreciable contacts are made with WEEV E2. Using these results, we generated a chimeric avian-mammalian MXRA8 decoy-receptor that neutralizes infection of multiple alphaviruses from distinct antigenic groups in vitro and in vivo. Thus, different alphaviruses can bind MXRA8 encoded by different vertebrate classes with distinct engagement modes, which enables development of broad-spectrum inhibitors.
期刊介绍:
Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO).
The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries.
In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.