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dc.contributor.authorCannone, Giuseppe
dc.contributor.authorKompaniiets, Dmytro
dc.contributor.authorGraham, Shirley
dc.contributor.authorWhite, Malcolm
dc.contributor.authorSpagnolo, Laura
dc.date.accessioned2023-02-20T12:30:07Z
dc.date.available2023-02-20T12:30:07Z
dc.date.issued2023-02-20
dc.identifier283306537
dc.identifierab7fc6ba-7b7c-49e8-b7fe-7991cefff8d6
dc.identifier85148366249
dc.identifier.citationCannone , G , Kompaniiets , D , Graham , S , White , M & Spagnolo , L 2023 , ' Structure of the Saccharolobus solfataricus type III-D CRISPR effector ' , Current Research in Structural Biology , vol. 5 , 100098 . https://doi.org/10.1016/j.crstbi.2023.100098en
dc.identifier.issn2665-928X
dc.identifier.otherORCID: /0000-0003-1543-9342/work/129709199
dc.identifier.otherORCID: /0000-0002-2608-3815/work/160753805
dc.identifier.urihttps://hdl.handle.net/10023/27016
dc.descriptionFunding: The authors acknowledge funding from BBSRC BB/J005673/1 project grant to LS and MFW and ERC funding to MFW (grant ref 101018608). DK was funded by a Darwin Trust of Edinburgh grant. We acknowledge Diamond Light Source for access and support of the cryo-EM facilities at the UK's national Electron Bio-imaging Centre (eBIC) under proposal EM16637-14, funded by the Wellcome Trust, MRC and BBRSC. The Scottish Centre for Macromolecular Imaging (SCMI) is funded by the MRC (MC_PC_17135) and SFC (H17007).en
dc.description.abstractCRISPR-Cas is a prokaryotic adaptive immune system, classified into six different types, each characterised by a signature protein. Type III systems, classified based on the presence of a Cas10 subunit, are rather diverse multi- subunit assemblies with a range of enzymatic activities and downstream ancillary effectors. The broad array of current biotechnological CRISPR applications is mainly based on proteins classified as Type II, however recent developments established the feasibility and efficacy of multi-protein Type III CRISPR-Cas effector complexes as RNA-targeting tools in eukaryotes. The crenarchaeon Saccharolobus solfataricus has two type III system subtypes (III- B and III-D). Here, we report the cryo-EM structure of the Csm Type III-D complex from S. solfataricus (SsoCsm), which uses CRISPR RNA to bind target RNA molecules, activating the Cas10 subunit for antiviral defence. The structure reveals the complex organisation, subunit/subunit connectivity and protein/guide RNA interactions of the SsoCsm complex, one of the largest CRISPR effectors known.
dc.format.extent8
dc.format.extent3716247
dc.language.isoeng
dc.relation.ispartofCurrent Research in Structural Biologyen
dc.subjectQH301 Biologyen
dc.subjectDASen
dc.subjectMCCen
dc.subject.lccQH301en
dc.titleStructure of the Saccharolobus solfataricus type III-D CRISPR effectoren
dc.typeJournal articleen
dc.contributor.sponsorEuropean Research Councilen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. St Andrews Bioinformatics Uniten
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1016/j.crstbi.2023.100098
dc.description.statusPeer revieweden
dc.identifier.grantnumber01018608en


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