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dc.contributor.authorSoh, Beatrice W
dc.contributor.authorKlotz, Alexander R
dc.contributor.authorRobertson-Anderson, Rae M
dc.contributor.authorDoyle, Patrick S
dc.date.accessioned2021-10-27T20:05:56Z
dc.date.available2021-10-27T20:05:56Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/134641
dc.description.abstract© 2019 American Physical Society. The entanglement of ring polymers remains mysterious in many aspects. In this Letter, we use electric fields to induce self-entanglements in circular DNA molecules, which serve as a minimal system for studying chain entanglements. We show that self-threadings give rise to entanglements in ring polymers and can slow down polymer dynamics significantly. We find that strongly entangled circular molecules remain kinetically arrested in a compact state for very long times, thereby providing experimental evidence for the severe topological constraints imposed by threadings.
dc.language.isoen
dc.publisherAmerican Physical Society (APS)
dc.relation.isversionof10.1103/PhysRevLett.123.048002
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourceAPS
dc.titleLong-Lived Self-Entanglements in Ring Polymers
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.relation.journalPhysical Review Letters
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-08-16T18:22:08Z
dspace.orderedauthorsSoh, BW; Klotz, AR; Robertson-Anderson, RM; Doyle, PS
dspace.date.submission2019-08-16T18:22:10Z
mit.journal.volume123
mit.journal.issue4
mit.metadata.statusAuthority Work and Publication Information Needed


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