Direct light-free cysteine-to-boronoalanine conversion in peptides
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Updated: Nov 5, 2026

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry
Published on: July 20, 2016
Jeongsu Lee1, Tomoko Hoshi1, Honami Matsumoto1
1Department of Pharmacy, Faculty of Pharmaceutical Sciences, Nagasaki International University, 2825-7 Huis Ten Bosch-machi, Sasebo, Nagasaki 859-3298, Japan. kyamada@niu.ac.jp.
Abstract:
Direct cysteine-to-boronoalanine conversion in peptides is achieved using B2cat2 and TPPTS in aqueous DMF/phosphate buffer at room temperature without irradiation. The method tolerates diverse peptide sequences, including methionine-containing and terminal-cysteine peptides, with no detectable epimerization or modification of other tested side chains.
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