Catalysis of Native Chemical Ligation and Expressed Protein Ligation by Alkylselenols.

The reaction between C-terminal α-thioester and N-terminal cysteinyl peptides is known as native chemical ligation (NCL). Alkyl α-thioesters are traditionally prepared in NCL due to their higher thermodynamic stability, which endows resistance to hydrolysis and easier peptide handling. However, the ligation kinetics of these species are slow, and the reaction times exceed the practical limits for chemical protein synthesis. Therefore, conversion to a more reactive phenyl α-thioesters through thiol-thioester exchange is usually employed to enhance the NCL reaction rate. In addition, phenyl thiols can reverse the formation of the less reactive branched thioesters, i.e., thioesters formed with internal Cys residues, and thiolactones. Interestingly, the fastest NCL rates are achieved with phenyl α-selenoesters, though phenylselenol is a poor catalyst for the selenol-(α-alkyl thioester) exchange, particularly with β-branched residues. Hence, it is usually necessary to preform the phenyl α-selenoester and protect internal cysteine residues to preserve the kinetic advantage. Moreover, an ∼2-5-fold excess of the N-terminal cysteine acceptor peptide is typically required to prevent the competition from the cysteine of the ligation product for the phenyl α-selenoester donor that leads to the branched thioester formation. Based on these precedents, we have designed sodium 2-selenoethanesulfonate (SeESNa) as a new selenol catalyst that can overcome these limitations. SeESNa reacts with alkyl α-thioester,