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Cited 30 time in webofscience Cited 32 time in scopus
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dc.contributor.authorSAMANIEGO, CHRISTIAN C-
dc.contributor.authorGIORDANO, GIULIA-
dc.contributor.authorKIM, JONGMIN-
dc.contributor.authorBLANCHINI, FRANCO-
dc.contributor.authorFRANCO, ELISA-
dc.date.accessioned2018-07-17T10:48:20Z-
dc.date.available2018-07-17T10:48:20Z-
dc.date.created2018-06-21-
dc.date.issued2016-04-
dc.identifier.issn2161-5063-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/92143-
dc.description.abstractMolecular titration is emerging as an important biochemical interaction mechanism within synthetic devices built with nucleic acids and the CRISPR/Cas system. We show that molecular titration in the context of feedback circuits is a suitable mechanism to enhance the emergence of oscillations and bistable behaviors. We consider biomolecular modules that can be inhibited or activated by input monomeric regulators; the regulators compete with constitutive titrating species to determine the activity of their target. By tuning the titration rate and the concentration of titrating species, it is possible to modulate the delay and convergence speed of the transient response, and the steepness and dead zone of the stationary response of the modules. These phenomena favor the occurrence of oscillations when modules are interconnected to create a negative feedback loop; bistability is favored in a positive feedback interconnection. Numerical simulations are supported by mathematical analysis showing that the capacity of the closed loop systems to exhibit oscillations or bistability is structural.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfACS Synthetic Biology-
dc.subjecttitration-
dc.subjectoscillations-
dc.subjectbistability-
dc.subjectmonomeric regulator-
dc.subjectdelays-
dc.subjectsynthetic biology-
dc.subjectRNA-
dc.titleMolecular Titration Promotes Oscillations and Bistability in Minimal Network Models with Monomeric Regulators-
dc.typeArticle-
dc.identifier.doi10.1021/acssynbio.5b00176-
dc.type.rimsART-
dc.identifier.bibliographicCitationACS Synthetic Biology, v.5, no.4, pp.321 - 333-
dc.identifier.wosid000374436400006-
dc.date.tcdate2019-01-01-
dc.citation.endPage333-
dc.citation.number4-
dc.citation.startPage321-
dc.citation.titleACS Synthetic Biology-
dc.citation.volume5-
dc.contributor.affiliatedAuthorKIM, JONGMIN-
dc.identifier.scopusid2-s2.0-84966397026-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc12-
dc.type.docTypeArticle-
dc.subject.keywordPlusTOGGLE SWITCH-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusELONGATION-
dc.subject.keywordPlusFEEDBACK-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusCIRCUIT-
dc.subject.keywordPlusCRISPR-
dc.subject.keywordAuthortitration-
dc.subject.keywordAuthoroscillations-
dc.subject.keywordAuthorbistability-
dc.subject.keywordAuthormonomeric regulator-
dc.subject.keywordAuthordelays-
dc.subject.keywordAuthorsynthetic biology-
dc.subject.keywordAuthorRNA-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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