Rapid on-resin N-formylation of peptides as one-pot reaction [research data]

N-formylation is a common pre- and post-translational modification of the N-terminus or the lysine side chain of peptides and proteins that plays a role in the initiation of immune responses, gene expression, or epigenetics. Despite its high biological relevance, protocols for the chemical N-formyla...

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Hauptverfasser: Kokollari, Agon (VerfasserIn) , Werner, Marius (VerfasserIn) , Lindner, Christina (VerfasserIn) , Pham, Truc Lam (VerfasserIn) , Thomas, Franziska (VerfasserIn)
Dokumenttyp: Datenbank Forschungsdaten
Sprache:Englisch
Veröffentlicht: Heidelberg Universität 2024-02-09
DOI:10.11588/data/00RULE
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Online-Zugang:Resolving-System, kostenfrei, Volltext: https://doi.org/10.11588/data/00RULE
Verlag, kostenfrei, Volltext: https://heidata.uni-heidelberg.de/dataset.xhtml?persistentId=doi:10.11588/data/00RULE
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Verfasserangaben:Agon Kokollari, Marius Werner, Christina Lindner, Truc Lam Pham, Franziska Thomas
Beschreibung
Zusammenfassung:N-formylation is a common pre- and post-translational modification of the N-terminus or the lysine side chain of peptides and proteins that plays a role in the initiation of immune responses, gene expression, or epigenetics. Despite its high biological relevance, protocols for the chemical N-formylation of synthetic peptides are scarce. The few available methods are elaborate in their execution and the yields are highly sequence-dependent. We present a rapid, easy-to-use one-pot procedure that runs at room temperature and can be used to formylate protected peptides at both the N-terminus and the lysine side chain on the resin in near-quantitative yields. Only insensitive, storage-stable standard chemicals – formic acid, acetic anhydride, pyridine and DMF – are used. Formylation works for both short and long peptides of up to 34 amino acids and over the spectrum of canonical amino acids.
Beschreibung:Gesehen am 12.02.2024
Beschreibung:Online Resource
DOI:10.11588/data/00RULE