Angewandte Chemie · 2021 · 13 citations · 27 references
Life SciencesBiochemistryMolecular BiologyPost-translational ModificationProtein EngineeringProteomicsPeptide Bond ChemistryPeptide ChemistryProtein DesignProtein StructureProtein S FunctionProtein-based Scaffolds
Abstract Post‐translational modifications (PTMs) enhance the repertoire of protein function and mediate or influence the activity of many cellular processes. The preparation of site‐specifically and homogeneously modified proteins, to apply as tools to understand the biological role of PTMs, is a challenging task. Herein, we describe a visible‐light‐mediated desulfurative C(sp 3 )–C(sp 3 ) bond forming reaction that enables the site‐selective installation of N ϵ ‐modified sidechains into peptides and proteins of interest. Rapid, operationally simple, and tolerant to ambient atmosphere, we demonstrate the installation of a range of lysine (Lys) PTMs into model peptide systems and showcase the potential of this technology by site‐selectively installing an N ϵ Ac sidechain into recombinantly expressed ubiquitin (Ub).
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Synthesis of Proteins by Native Chemical Ligation
Philip E. Dawson, Tom W. Muir, Ian Clark‐Lewis et al. · Science · 1994 · 4.1K citations
How many human proteoforms are there?
Ruedi Aebersold, Jeffrey N. Agar, I. Jonathan Amster et al. · Nature Chemical Biology · 2018 · 944 citations · Full text