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dc.contributor.authorGam, Jeremy J.
dc.contributor.authorDiAndreth, Breanna
dc.contributor.authorJones, Ross D.
dc.contributor.authorHuh, Jin
dc.contributor.authorWeiss, Ron
dc.date.accessioned2020-04-08T17:13:28Z
dc.date.available2020-04-08T17:13:28Z
dc.date.issued2019-08
dc.date.submitted2019-01
dc.identifier.issn1362-4962
dc.identifier.issn0305-1048
dc.identifier.urihttps://hdl.handle.net/1721.1/124540
dc.description.abstractBiological research is relying on increasingly complex genetic systems and circuits to perform sophisticated operations in living cells. Performing these operations often requires simultaneous delivery of many genes, and optimizing the stoichiometry of these genes can yield drastic improvements in performance. However, sufficiently sampling the large design space of gene expression stoichiometries in mammalian cells using current methods is cumbersome, complex, or expensive. We present a 'poly-transfection' method as a simple yet high-throughput alternative that enables comprehensive evaluation of genetic systems in a single, readily-prepared transfection sample. Each cell in a poly-transfection represents an independent measurement at a distinct gene expression stoichiometry, fully leveraging the single-cell nature of transfection experiments. We first benchmark poly-transfection against co-transfection, showing that titration curves for commonly-used regulators agree between the two methods. We then use poly-transfections to efficiently generate new insights, for example in CRISPRa and synthetic miRNA systems. Finally, we use poly-transfection to rapidly engineer a difficult-to-optimize miRNA-based cell classifier for discriminating cancerous cells. One-pot evaluation enabled by poly-transfection accelerates and simplifies the design of genetic systems, providing a new high-information strategy for interrogating biology. ©2019en_US
dc.description.sponsorshipNational Institutes of Health (no. R01CA173712)en_US
dc.description.sponsorshipNational Institutes of Health (no. R01CA207029)en_US
dc.description.sponsorshipNational Institutes of Health (no. P50GM098792)en_US
dc.description.sponsorshipNational Science Foundation (no. 1745645)en_US
dc.description.sponsorshipCancer Center Support Grant (no. P30CCA14051)en_US
dc.language.isoen
dc.publisherOxford University Press (OUP)en_US
dc.relation.isversionof10.1093/NAR/GKZ623en_US
dc.rightsCreative Commons Attribution NonCommercial License 4.0en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.sourceOxford University Pressen_US
dc.titleA ‘poly-transfection’ method for rapid, one-pot characterization and optimization of genetic systemsen_US
dc.typeArticleen_US
dc.identifier.citationGam, Jeremy J., et al., "A ‘poly-transfection’ method for rapid, one-pot characterization and optimization of genetic systems." Nucleic acids research 47, 18 (August 2019): p. e106 doi 10.1093/NAR/GKZ623 ©2019 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalNucleic acids researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-03-19T12:16:58Z
dspace.date.submission2020-03-19T12:17:02Z
mit.journal.volume47en_US
mit.journal.issue18en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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