Abstract
An efficient strategy for the synthesis of large libraries of conformationally defined peptides is reported, using dynamic combinatorial chemistry as a tool to graft amino acid side chains on a well-ordered 3D (3-dimension) peptide backbone. Combining rationally designed scaffolds with combinatorial side chains selection represents an alternative method to access peptide libraries for structures that are not genetically encodable. This method would allow a breakthrough for the discovery of protein mimetic for unconventional targets for which little is known.
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Zagiel, B., Peker, T., Marquant, R., Cazals, G., Webb, G., Miclet, E., … Moumné, R. (2022). Dynamic Amino Acid Side-Chains Grafting on Folded Peptide Backbone**. Chemistry - A European Journal, 28(36). https://doi.org/10.1002/chem.202200454
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