Catalysis of native chemical ligation and expressed protein ligation by alkylselenols

Vista senzilla d'ítem
dc.contributor.authorSánchez Campillo, Iván
dc.contributor.authorGratacòs i Batlle, Esther
dc.contributor.authorPérez García, Selene
dc.contributor.authorNguyen, Hong S.
dc.contributor.authorTriola i Guillem, Gemma
dc.contributor.authorMootz, Henning D.
dc.contributor.authorBlanco Canosa, Juan B.
dc.date.accessioned2025-12-04T10:08:25Z
dc.date.available2025-12-04T10:08:25Z
dc.date.issued2025-12-02
dc.description.sponsorshipThe reaction between C-terminal α-thioester and N-terminal cysteinyl peptides is known as native chemical ligation (NCL). Alkyl α-thioesters are traditionally prepared in NCL due to their higher thermodynamic stability, which endows resistance to hydrolysis and easier peptide handling. However, the ligation kinetics of these species are slow, and the reaction times exceed the practical limits for chemical protein synthesis. Therefore, conversion to a more reactive phenyl α-thioesters through thiol-thioester exchange is usually employed to enhance the NCL reaction rate. In addition, phenyl thiols can reverse the formation of the less reactive branched thioesters, i.e., thioesters formed with internal Cys residues, and thiolactones. Interestingly, the fastest NCL rates are achieved with phenyl α-selenoesters, though phenylselenol is a poor catalyst for the selenol-(α-alkyl thioester) exchange, particularly with β-branched residues. Hence, it is usually necessary to preform the phenyl α-selenoester and protect internal cysteine residues to preserve the kinetic advantage. Moreover, an ∼2–5-fold excess of the N-terminal cysteine acceptor peptide is typically required to prevent the competition from the cysteine of the ligation product for the phenyl α-selenoester donor that leads to the branched thioester formation. Based on these precedents, we have designed sodium 2-selenoethanesulfonate (SeESNa) as a new selenol catalyst that can overcome these limitations. SeESNa reacts with alkyl α-thioester, N-acyl benzotriazole, and N-acylurea peptides, giving α-SeESNa species. We have determined the rate constants for the ligation with preformed α-SeESNa peptides and show that it is a superior catalyst compared to the known 4-mercaptophenylacetic and 4-mercaptobenzoic acids. The utility of SeESNA was proved through the synthesis of the cardiotoxin A5, a snake venom peptide that contains eight cysteines, without orthogonal cysteine protection. Importantly, it has enabled expressed protein ligation under folding conditions with extraordinary speed, as shown with the Sonic Hedgehog and SUMO2 proteins. Thus, SeESNa is envisaged to have broad applicability in synthetic and semisynthetic protein chemistry.
dc.format.extent17 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn2691-3704
dc.identifier.urihttps://hdl.handle.net/2445/224669
dc.language.isoeng
dc.publisherACS Publications
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1021/jacsau.5c00793
dc.relation.ispartofJACS Au, 2025
dc.relation.urihttps://doi.org/10.1021/jacsau.5c00793
dc.rightscc-by (c) Sánchez Campillo, Iván et al., 2025
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.classificationLligands
dc.subject.classificationModificació química de les proteïnes
dc.subject.classificationPèptids
dc.subject.otherLigands
dc.subject.otherChemical modification of proteins
dc.subject.otherPeptides
dc.titleCatalysis of native chemical ligation and expressed protein ligation by alkylselenols
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Miniatura
Nom:
catalysis-of-native-chemical-ligation-and-expressed-protein-ligation-by-alkylselenols.pdf
Mida:
6.29 MB
Format:
Adobe Portable Document Format
Descarregar

Col·leccions

Articles publicats en revistes (Química Inorgànica i Orgànica)