| Literature DB >> 29516601 |
Philip A Cistrone1, Anthony P Silvestri1, Jordi C J Hintzen1, Philip E Dawson1.
Abstract
Peptide macrocycles are widely utilized in the development of high affinity ligands, including stapled α-helices. The linear rigidity of a 1,3-diynyl linkage provides an optimal distance (7 Å) between β-carbons of the i,i+4 amino acid side chains, thus suggesting its utility in stabilizing α-helical structures. Here, we report the development of an on-resin strategy for an intramolecular Glaser reaction between two alkyne-terminated side chains by using copper chloride, an essential bpy-diol ligand, and diisopropylethylamine at room temperature. The efficiency of this ligation was illustrated by the synthesis of (i,i+4)-, (i,i+5)-, (i,i+6)-, and (i,i+7)-stapled BCL-9 α-helical peptides using the unnatural amino acid propargyl serine. Overall, this procedurally simple method relies on inexpensive and widely available reagents to generate low molecular weight 23-, 26-, 29-, and 32-membered peptide macrocycles.Entities:
Keywords: Glaser; chemoselectivity; copper acetylide; macrocyclization; peptide stapling
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Year: 2018 PMID: 29516601 PMCID: PMC6097620 DOI: 10.1002/cbic.201800121
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164