Enzyme-catalyzed macrocyclization of long unprotected peptides

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Abstract

A glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective SNAr reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on the same polypeptide chain. Cyclic peptides ranging from 9 to 24 residues were quantitatively produced within 2 h in aqueous pH = 8 buffer at room temperature. The reaction was highly selective for cyclization at the GSH tag, enabling the combination of GST-catalyzed ligation with native chemical ligation to generate a large 40-residue peptide macrocycle. © 2014 American Chemical Society.

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Zhang, C., Dai, P., Spokoyny, A. M., & Pentelute, B. L. (2014). Enzyme-catalyzed macrocyclization of long unprotected peptides. Organic Letters, 16(14), 3652–3655. https://doi.org/10.1021/ol501609y

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