Extendable stapling of unprotected peptides by crosslinking two amines with o-phthalaldehyde

• Published in: Nature communications 2022-01, Vol.13 (1), p.311-311, Article 311
• Main Authors: Li, Bo, Wang, Lan, Chen, Xiangxiang, Chu, Xin, Tang, Hong, Zhang, Jie, He, Gang, Li, Li, Chen, Gong
• Format: Article
• Language: English
• Subjects: 639/638/403/933; 639/638/92/611; Amines; Amino acids; Amino groups; Crosslinking; Cysteine; Humanities and Social Sciences; multidisciplinary; Peptides; Reagents; Residues; Science; Science (multidisciplinary); Substrates
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-022-27985-7

Peptide modification methods that do not rely on the cysteine residue are underdeveloped, and their development could greatly expand the current toolbox for peptide chemistry. During the course of preliminary investigations into the classical ortho -phthalaldehyde (OPA)-amine-thiol condensation reaction, we found that in the absence of thiol, OPA readily condenses with two primary alkyl amines to form a class of underexplored isoindolin-1-imine compounds under mild aqueous conditions. From the intramolecular version of this OPA-2amines reaction, an efficient and selective methodology using mild reaction conditions has been developed for stapling unprotected peptides via crosslinking of two amino groups in both an end-to-side and side-to-side fashion. The stapling method is superfast and broadly applicable for various peptide substrates with the reacting amino groups separated by a wide range of different amino acid units. The macrocyclization reactions of selected substrates are completed within 10 seconds at 5 mM concentration and within 2 minutes at 50 μM concentration. Importantly, the resulting cyclized peptides with an isoindolinimine linkage can be extended in a one-pot sequential addition manner with several different electron-deficient π electrophiles, thereby generating more complex structures. Methods for peptide stapling, or covalently linking amino acid residues to create a non-linear structure, mostly rely on cysteine residues, which imposes a significant practical limitation. Here the authors disclose a method to chemoselectively macrocyclize two free-amine-containing residues in mild, peptide-relevant conditions, using a commercially available reagent.