Wehofsky Nicole, Wespe Christian, Cerovsky Vaclav, Pech Andreas, Hoess Eva, Rudolph Rainer, Bordusa Frank
Max Planck Research Unit for Enzymology of Protein Folding, Weinbergweg 22, 06120 Halle/Saale, Germany.
Chembiochem. 2008 Jun 16;9(9):1493-9. doi: 10.1002/cbic.200800025.
Herein we present the first report on protease-catalysed ligation of cleavage-sensitive peptide and protein fragments in ionic-liquid-containing solvent systems. By applying the newly established [MMIM][Me2PO4]/buffer mixture as a reaction medium, significant advantages over purely aqueous or conventional organic solvent-containing media could be identified, including in particular the use of active wild-type proteases as biocatalysts, the suppression of any competitive proteolytic side reactions, the high turnover rates compared to classical organic solvents and the high stability of chemically labile reactants.
在此,我们首次报道了在含离子液体的溶剂体系中蛋白酶催化切割敏感肽和蛋白质片段的连接反应。通过应用新建立的[MMIM][Me2PO4]/缓冲液混合物作为反应介质,可以发现相对于纯水性或传统含有机溶剂的介质具有显著优势,尤其包括使用活性野生型蛋白酶作为生物催化剂、抑制任何竞争性蛋白水解副反应、与经典有机溶剂相比具有高周转率以及化学不稳定反应物的高稳定性。