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Self-Assembly of Catenanes from Lasso Peptides

Author(s): Allen, Caitlin D.; Link, A. James

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dc.contributor.authorAllen, Caitlin D.-
dc.contributor.authorLink, A. James-
dc.date.accessioned2020-01-31T20:28:10Z-
dc.date.available2020-01-31T20:28:10Z-
dc.date.issued2016-11-02en_US
dc.identifier.citationAllen, Caitlin D., Link, A. James. (2016). Self-Assembly of Catenanes from Lasso Peptides. Journal of the American Chemical Society, 138 (43), 14214 - 14217. doi:10.1021/jacs.6b09454en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1nb54-
dc.description.abstractLasso peptides exist naturally in a threaded state as [1]rotaxanes, and we reasoned that lasso peptides cleaved in their loop region could serve as building blocks for catenanes. Mutagenesis of the lasso peptide microcin J25 (MccJ25) with two cysteine residues followed by cleavage of the peptide with trypsin led to a [2]rotaxane structure that self-assembled into a [3]catenane and [4]catenanes at room temperature in aqueous solution. The [3]catenane represents the smallest ring size of a catenane comprised solely of polypeptide segments. The NMR structure of the [3]catenane was determined, suggesting that burial of hydrophobic residues may be a driving force for assembly of the catenane structure.en_US
dc.format.extent14214 - 14217en_US
dc.language.isoen_USen_US
dc.relation.ispartofJournal of the American Chemical Societyen_US
dc.rightsAuthor's manuscripten_US
dc.titleSelf-Assembly of Catenanes from Lasso Peptidesen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1021/jacs.6b09454-
dc.date.eissued2016-10-21en_US
dc.identifier.eissn1520-5126-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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