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Water-soluble allyl sulfones for dual site-specific labelling of proteins and cyclic peptides

Water-soluble allyl sulfones provide convenient site-specific disulfide rebridging of native proteins and cyclic peptides. The site-selective functionalization of (a) the peptide hormone somatostatin, (b) the interchain disulfide of bovine insulin and (c) functionalization of the proteins GFP and ly...

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Detalles Bibliográficos
Autores principales: Wang, Tao, Riegger, Andreas, Lamla, Markus, Wiese, Sebastian, Oeckl, Patrick, Otto, Markus, Wu, Yuzhou, Fischer, Stephan, Barth, Holger, Kuan, Seah Ling, Weil, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006486/
https://www.ncbi.nlm.nih.gov/pubmed/29997815
http://dx.doi.org/10.1039/c6sc00005c
Descripción
Sumario:Water-soluble allyl sulfones provide convenient site-specific disulfide rebridging of native proteins and cyclic peptides. The site-selective functionalization of (a) the peptide hormone somatostatin, (b) the interchain disulfide of bovine insulin and (c) functionalization of the proteins GFP and lysozyme with allyl sulfones proceeds in aqueous solution. Allyl sulfones offer three functionalizable sites that react with thiol containing molecules in a step-wise fashion. Dual labeling of proteins and cyclic peptides is achieved i.e. the attachment of a chromophore and an affinity tag in a single reaction step, which is of great significance for the construction of precise multifunctional peptide and protein conjugates.