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dc.contributor.authorMa, Hanhui
dc.contributor.authorTu, Li-Chun
dc.contributor.authorNaseri, Ardalan
dc.contributor.authorChung, Yu-Chieh
dc.contributor.authorGrunwald, David
dc.contributor.authorZhang, Shaojie
dc.contributor.authorPederson, Thoru
dc.date2022-08-11T08:10:52.000
dc.date.accessioned2022-08-23T17:22:56Z
dc.date.available2022-08-23T17:22:56Z
dc.date.issued2018-11-01
dc.date.submitted2019-09-18
dc.identifier.citation<p>Nat Methods. 2018 Nov;15(11):928-931. doi: 10.1038/s41592-018-0174-0. Epub 2018 Oct 30. <a href="https://doi.org/10.1038/s41592-018-0174-0">Link to article on publisher's site</a></p>
dc.identifier.issn1548-7091 (Linking)
dc.identifier.doi10.1038/s41592-018-0174-0
dc.identifier.pmid30377374
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48850
dc.description.abstractClustered regularly interspaced short palindromic repeats (CRISPR) guide RNA scaffolds have been adapted to carry multiple binding sites for fluorescent proteins to enhance brightness for live cell imaging of genomic loci. However, many of these modifications result in guide RNA instability and thus produce lower genome-labeling efficiency than anticipated. Here we introduce CRISPR-Sirius, based on octet arrays of aptamers conferring both enhanced guide RNA stability and brightness, and provide initial biological applications of this platform.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30377374&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252086/
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectBioimaging and Biomedical Optics
dc.subjectGenetics and Genomics
dc.titleCRISPR-Sirius: RNA scaffolds for signal amplification in genome imaging
dc.typeJournal Article
dc.source.journaltitleNature methods
dc.source.volume15
dc.source.issue11
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/rti_pubs/59
dc.identifier.contextkey15358659
html.description.abstract<p>Clustered regularly interspaced short palindromic repeats (CRISPR) guide RNA scaffolds have been adapted to carry multiple binding sites for fluorescent proteins to enhance brightness for live cell imaging of genomic loci. However, many of these modifications result in guide RNA instability and thus produce lower genome-labeling efficiency than anticipated. Here we introduce CRISPR-Sirius, based on octet arrays of aptamers conferring both enhanced guide RNA stability and brightness, and provide initial biological applications of this platform.</p>
dc.identifier.submissionpathrti_pubs/59
dc.contributor.departmentRNA Therapeutics Institute
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages928-931


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