Vinylphosphonites for staudinger-induced chemoselective peptide cyclization and functionalization

Item Type: | Article |
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Title: | Vinylphosphonites for staudinger-induced chemoselective peptide cyclization and functionalization |
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Creators Name: | Kasper, M.A and Glanz, M. and Oder, A. and Schmieder, P. and von Kries, J.P. and Hackenberger, C.P.R. |
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Abstract: | In this paper, we introduce vinylphosphonites for chemoselective Staudinger-phosphonite reactions (SPhR) with azides to form vinylphosphonamidates for the subsequent modification of cysteine residues in peptides and proteins. An electron-rich alkene is turned into an electron-deficient vinylphosphonamidate, thereby inducing electrophilic reactivity for a following thiol addition. We show that by varying the phosphonamidate ester substituent we can fine-tune the reactivity of the thiol addition and even control the functional properties of the final conjugate. Furthermore, we observed a drastic increase in thiol addition efficiency when the SPhR is carried out in the presence of a thiol substrate in a one-pot reaction. Hence, we utilize vinylphosphonites for the chemoselective intramolecular cyclization of peptides carrying an azide-containing amino acid and a cysteine in high yields. Our concept was demonstrated for the stapling of a cell-permeable peptidic inhibitor for protein–protein interaction (PPI) between BCL9 and beta-catenin, which is known to create a transcription factor complex playing a role in embryonic development and cancer origin, and for macrocyclization of cell-penetrating peptides (CPPs) to enhance the cellular uptake of proteins. |
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Keywords: | Protein Modification, Drug, Strategies, Stability, Chemistry |
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Source: | Chemical Science |
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ISSN: | 2041-6520 |
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Publisher: | Royal Society of Chemistry |
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Volume: | 10 |
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Number: | 25 |
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Page Range: | 6322-6329 |
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Date: | 7 July 2019 |
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Official Publication: | https://doi.org/10.1039/C9SC01345H |
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PubMed: | View item in PubMed |
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