Show simple item record

dc.contributor.authorZhang, Chi
dc.contributor.authorDai, Peng
dc.contributor.authorSpokoyny, Alexander M.
dc.contributor.authorPentelute, Bradley L.
dc.date.accessioned2016-10-13T20:17:20Z
dc.date.available2016-10-13T20:17:20Z
dc.date.issued2014-07
dc.date.submitted2014-05
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttp://hdl.handle.net/1721.1/104805
dc.description.abstractA glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective SNAr reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on the same polypeptide chain. Cyclic peptides ranging from 9 to 24 residues were quantitatively produced within 2 h in aqueous pH = 8 buffer at room temperature. The reaction was highly selective for cyclization at the GSH tag, enabling the combination of GST-catalyzed ligation with native chemical ligation to generate a large 40-residue peptide macrocycle.en_US
dc.description.sponsorshipMassachusetts Institute of Technology (MIT startup funds)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant GM101762)en_US
dc.description.sponsorshipDamon Runyon Cancer Research Foundation (Award)en_US
dc.description.sponsorshipSontag Foundation (Distinguished Scientist Award)en_US
dc.description.sponsorshipAmgen Inc. (Summer Graduate Research Fellowship)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol501609yen_US
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.en_US
dc.sourceACSen_US
dc.titleEnzyme-Catalyzed Macrocyclization of Long Unprotected Peptidesen_US
dc.typeArticleen_US
dc.identifier.citationZhang, Chi, Peng Dai, Alexander M. Spokoyny, and Bradley L. Pentelute. “Enzyme-Catalyzed Macrocyclization of Long Unprotected Peptides.” Organic Letters 16, no. 14 (July 18, 2014): 3652–3655.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorZhang, Chi
dc.contributor.mitauthorDai, Peng
dc.contributor.mitauthorSpokoyny, Alexander M.
dc.contributor.mitauthorPentelute, Bradley L.
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5253-6873
dc.identifier.orcidhttps://orcid.org/0000-0002-4581-3473
mit.licensePUBLISHER_POLICYen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record