Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103799
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dc.contributor.authorRawling, David C.en
dc.contributor.authorKohlway, Andrew S.en
dc.contributor.authorLuo, Dahaien
dc.contributor.authorDing, Steve C.en
dc.contributor.authorPyle, Anna Marieen
dc.date.accessioned2015-01-12T04:35:16Zen
dc.date.accessioned2019-12-06T21:20:31Z-
dc.date.available2015-01-12T04:35:16Zen
dc.date.available2019-12-06T21:20:31Z-
dc.date.copyright2014en
dc.date.issued2014en
dc.identifier.citationRawling, D. C., Kohlway, A. S., Luo, D., Ding, S. C., & Pyle, A. M. (2014). The RIG-I ATPase core has evolved a functional requirement for allosteric stabilization by the Pincer domain. Nucleic acids research, 42(18), 11601-11611.en
dc.identifier.issn0305-1048en
dc.identifier.urihttps://hdl.handle.net/10356/103799-
dc.description.abstractRetinoic acid-inducible gene I (RIG-I) is a pattern recognition receptor expressed in metazoan cells that is responsible for eliciting the production of type I interferons and pro-inflammatory cytokines upon detection of intracellular, non-self RNA. Structural studies of RIG-I have identified a novel Pincer domain composed of two alpha helices that physically tethers the C-terminal domain to the SF2 helicase core. We find that the Pincer plays an important role in mediating the enzymatic and signaling activities of RIG-I. We identify a series of mutations that additively decouple the Pincer motif from the ATPase core and show that this decoupling results in impaired signaling. Through enzymological and biophysical analysis, we further show that the Pincer domain controls coupled enzymatic activity of the protein through allosteric control of the ATPase core. Further, we show that select regions of the HEL1 domain have evolved to potentiate interactions with the Pincer domain, resulting in an adapted ATPase cleft that is now responsive to adjacent domains that selectively bind viral RNA.en
dc.format.extent11 p.en
dc.language.isoenen
dc.relation.ispartofseriesNucleic acids researchen
dc.rights© 2014 The Author(s). Published by Oxford University Press on behalf of Nucleic Acids Research. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectDRNTU::Science::Medicineen
dc.titleThe RIG-I ATPase core has evolved a functional requirement for allosteric stabilization by the Pincer domainen
dc.typeJournal Articleen
dc.contributor.schoolLee Kong Chian School of Medicine (LKCMedicine)en
dc.identifier.doi10.1093/nar/gku817en
dc.description.versionPublished versionen
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Appears in Collections:LKCMedicine Journal Articles
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