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dc.contributor.authorTamsir, Alvin
dc.contributor.authorClancy, Kevin
dc.contributor.authorPeterson, Todd
dc.contributor.authorStanton, Brynne C.
dc.contributor.authorNielsen, Alec Andrew
dc.contributor.authorVoigt, Christopher A.
dc.date.accessioned2015-10-30T15:51:51Z
dc.date.available2015-10-30T15:51:51Z
dc.date.issued2013-12
dc.date.submitted2013-08
dc.identifier.issn1552-4450
dc.identifier.issn1552-4469
dc.identifier.urihttp://hdl.handle.net/1721.1/99526
dc.description.abstractGenetic circuits perform computational operations based on interactions between freely diffusing molecules within a cell. When transcription factors are combined to build a circuit, unintended interactions can disrupt its function. Here, we apply 'part mining' to build a library of 73 TetR-family repressors gleaned from prokaryotic genomes. The operators of a subset were determined using an in vitro method, and this information was used to build synthetic promoters. The promoters and repressors were screened for cross-reactions. Of these, 16 were identified that both strongly repress their cognate promoter (5- to 207-fold) and exhibit minimal interactions with other promoters. Each repressor-promoter pair was converted to a NOT gate and characterized. Used as a set of 16 NOT/NOR gates, there are >10[superscript 54] circuits that could be built by changing the pattern of input and output promoters. This represents a large set of compatible gates that can be used to construct user-defined circuits.en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (Award FA9550-11-C-0028)en_US
dc.description.sponsorshipAmerican Society for Engineering Education. National Defense Science and Engineering Graduate Fellowship (32 CFR 168a)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency. Chronical of Lineage Indicative of Origins (N66001-12-C-4016)en_US
dc.description.sponsorshipUnited States. Office of Naval Research (N00014-13-1-0074)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (GM095765)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Synthetic Biology Engineering Research Center (SA5284-11210)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nchembio.1411en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleGenomic mining of prokaryotic repressors for orthogonal logic gatesen_US
dc.typeArticleen_US
dc.identifier.citationStanton, Brynne C, Alec A K Nielsen, Alvin Tamsir, Kevin Clancy, Todd Peterson, and Christopher A Voigt. “Genomic Mining of Prokaryotic Repressors for Orthogonal Logic Gates.” Nat Chem Biol 10, no. 2 (December 8, 2013): 99–105.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Biology Centeren_US
dc.contributor.mitauthorStanton, Brynne C.en_US
dc.contributor.mitauthorNielsen, Alec Andrewen_US
dc.contributor.mitauthorVoigt, Christopher A.en_US
dc.relation.journalNature Chemical Biologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsStanton, Brynne C; Nielsen, Alec A K; Tamsir, Alvin; Clancy, Kevin; Peterson, Todd; Voigt, Christopher Aen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0844-4776
dc.identifier.orcidhttps://orcid.org/0000-0003-2171-8460
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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