| Literature DB >> 25591010 |
Emmanuelle Boll1, Hervé Drobecq1, Nathalie Ollivier1, Annick Blanpain1, Laurent Raibaut1, Rémi Desmet1, Jérôme Vicogne1, Oleg Melnyk1.
Abstract
Small ubiquitin-like modifier (SUMO) post-translational modification (PTM) of proteins has a crucial role in the regulation of important cellular processes. This protocol describes the chemical synthesis of functional SUMO-peptide conjugates. The two crucial stages of this protocol are the solid-phase synthesis of peptide segments derivatized by thioester or bis(2-sulfanylethyl)amido (SEA) latent thioester functionalities and the one-pot assembly of the SUMO-peptide conjugate by a sequential native chemical ligation (NCL)/SEA native peptide ligation reaction sequence. This protocol also enables the isolation of a SUMO SEA latent thioester, which can be attached to a target peptide or protein in a subsequent step. It is compatible with 9-fluorenylmethoxycarbonyl (Fmoc) chemistry, and it gives access to homogeneous, reversible and functional SUMO conjugates that are not easily produced using living systems. The synthesis of SUMO-peptide conjugates on a milligram scale takes 20 working days.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25591010 DOI: 10.1038/nprot.2015.013
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491