Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/84599
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dc.contributor.authorQiu, Yiboen
dc.contributor.authorNguyen, Giang Kien Trucen
dc.contributor.authorCao, Yuanen
dc.contributor.authorHemu, Xinyaen
dc.contributor.authorLiu, Chuan-Faen
dc.contributor.authorTam, James Pingkwanen
dc.date.accessioned2016-12-16T08:57:09Zen
dc.date.accessioned2019-12-06T15:48:03Z-
dc.date.available2016-12-16T08:57:09Zen
dc.date.available2019-12-06T15:48:03Z-
dc.date.issued2016en
dc.identifier.citationNguyen, G. K. T., Qiu, Y., Cao, Y., Hemu, X., Liu, C. -F., & Tam, J. P. (2016). Butelase-mediated cyclization and ligation of peptides and proteins. Nature Protocols, 11(10), 1977-1988.en
dc.identifier.issn1754-2189en
dc.identifier.urihttps://hdl.handle.net/10356/84599-
dc.description.abstractEnzymes that catalyze efficient macrocyclization or site-specific ligation of peptides and proteins can enable tools for drug design and protein engineering. Here we describe a protocol to use butelase 1, a recently discovered peptide ligase, for high-efficiency cyclization and ligation of peptides and proteins ranging in size from 10 to >200 residues. Butelase 1 is the fastest known ligase and is found in pods of the common medicinal plant Clitoria ternatea (also known as butterfly pea). It has a very simple C-terminal-specific recognition motif that requires Asn/Asp (Asx) at the P1 position and a dipeptide His–Val at the P1′ and P2′ positions. Substrates for butelase-mediated ligation can be prepared by standard Fmoc (9-fluorenylmethyloxycarbonyl) chemistry or recombinant expression with the minimal addition of this tripeptide Asn–His–Val motif at the C terminus. Butelase 1 achieves cyclizations that are 20,000 times faster than those of sortase A, a commonly used enzyme for backbone cyclization. Unlike sortase A, butelase is traceless, and it can be used for the total synthesis of naturally occurring peptides and proteins. Furthermore, butelase 1 is also useful for intermolecular ligations and synthesis of peptide or protein thioesters, which are versatile activated intermediates necessary for and compatible with many chemical ligation methods. The protocol describes steps for isolation and purification of butelase 1 from plant extract using a four-step chromatography procedure, which takes ~3 d. We then describe steps for intramolecular cyclization, intermolecular ligation and butelase-mediated synthesis of protein thioesters. Butelase reactions are generally completed within minutes and often achieve excellent yields.en
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en
dc.format.extent21 p.en
dc.language.isoenen
dc.relation.ispartofseriesNature Protocolsen
dc.rights© 2016 Nature Publishing Group. This is the author created version of a work that has been peer reviewed and accepted for publication by Nature Protocols, Nature Publishing Group. 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/10.1038/nprot.2016.118].en
dc.subjectButelaseen
dc.subjectCyclizationen
dc.titleButelase-mediated cyclization and ligation of peptides and proteinsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doi10.1038/nprot.2016.118en
dc.description.versionAccepted versionen
item.grantfulltextopen-
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