1. Controlled co-immobilisation of proteins via 4′-phosphopantetheine-mediated site-selective covalent linkage
- Author
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Yujiao, Zheng, Wenshi, Luo, Jia, Yang, Huazhen, Wang, Quan, Hu, Zaohai, Zeng, Xuefeng, Li, and Shengbin, Wang
- Subjects
Bioengineering ,General Medicine ,Molecular Biology ,Biotechnology - Abstract
In Escherichia coli, acyl carrier protein (ACP) is posttranslationally converted into its active holo-ACP form via covalent linkage of 4'-phosphopantetheine (4'-PP) to residue serine-36. We found that the long flexible 4'-PP arm could react chemoselectively with the iodoacetyl group introduced on solid supports with high efficiency under mild conditions. Based on this finding, we developed site-selective immobilisation of proteins via the active holo-ACP fusion tag, independently of the physicochemical properties of the protein of interest. Furthermore, the molecular ratios of co-immobilised proteins can be manipulated because the tethering process is predominantly directed by the molar concentrations of diverse holo-ACP fusions during co-immobilisation. Conveniently tuning the molecular ratios of co-immobilised proteins allows their cooperation, leading to a highly productive multi-protein co-immobilisation system. Kinetic studies of enzymes demonstrated that α-amylase (Amy) and methyl parathion hydrolase (MPH) immobilised via active tag holo-ACP had higher catalytic efficiency (k
- Published
- 2022
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