dc.contributor.authorHemu, Xinya
dc.contributor.authorTaichi, Misako
dc.contributor.authorQiu, Yibo
dc.contributor.authorLiu, Ding-Xiang
dc.contributor.authorTam, James P.
dc.date.accessioned2016-01-13T03:02:07Z
dc.date.available2016-01-13T03:02:07Z
dc.date.issued2013
dc.identifier.citationHemu, X., Taichi, M., Qiu, Y., Liu, D.-X., & Tam, J. P. (2013). Biomimetic synthesis of cyclic peptides using novel thioester surrogates. Biopolymers, 100(5), 492-501.en_US
dc.identifier.issn0006-3525en_US
dc.identifier.urihttp://hdl.handle.net/10220/39685
dc.description.abstractAcyl shifts involving N-S and S-S rearrangements are reactions central to the breaking of a peptide bond and forming of thioester intermediates in an intein-catalyzed protein splicing that ultimately leads to the formation of a new peptide bond by an uncatalyzed S-N acyl shift reaction. To mimic these three acyl shift reactions in forming thioesters and the subsequent peptide ligation, here we describe the development of two 9-fluorenylmethoxycarbonyl (Fmoc)-compatible thioester surrogates that can undergo uncatalyzed N-S, S-S, and S-N acyl shifts for preparing thioesters and cyclic peptides. These surrogates were incorporated as a C-terminal amido moiety of a target peptide using Fmoc chemistry by solid-phase synthesis, and then transformed into a thioester or thiolactones via two acyl shift reactions with or without the presence of an external thiol under acidic conditions. The proposed intein-mimetic thioester surrogates were prepared using readily available starting materials including N-methyl cysteine or 2-thioethylbutylamide. A key functional moiety shared in their design is the thioethylamido (TEA) moiety, which is essential to effect a proximity-driven N-S acyl shift under a favorable five-member ring transition in the breaking of a peptide bond. Thus, the tandem series of acyl shifts effected by a TEA moiety in a thioester surrogate together with a thioethylamino moiety of an N-terminal Cys residue in a linear peptide precursor are chemical mimics of an intein, as they mediate both excision and ligation reactions in forming cyclic peptides including cyclic conotoxin and sunflower trypsin inhibitor described herein.en_US
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en_US
dc.description.sponsorshipASTAR (Agency for Sci., Tech. and Research, S’pore)en_US
dc.format.extent17 p.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesBiopolymersen_US
dc.rights© 2013 Wiley Periodicals, Inc. This is the author created version of a work that has been peer reviewed and accepted for publication by Biopolymers, Wiley Periodicals, Inc. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1002/bip.22308].en_US
dc.subjectThioesteren_US
dc.subjectThioethylamido
dc.subjectThioester surrogate
dc.subjectN-S acyl shift
dc.subjectIntein mimetic
dc.subjectCyclic peptides
dc.subjectConotoxin
dc.subjectSunflower trypsin inhibitor
dc.titleBiomimetic synthesis of cyclic peptides using novel thioester surrogatesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1002/bip.22308
dc.description.versionAccepted versionen_US


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