Use of the amicyanin signal sequence for efficient periplasmic expression in E. coli of a human antibody light chain variable domain.

Autor: Dow BA; Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, United States., Tatulian SA; Department of Physics, University of Central Florida, Orlando, FL 32816, United States., Davidson VL; Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, United States. Electronic address: victor.davidson@ucf.edu.
Jazyk: angličtina
Zdroj: Protein expression and purification [Protein Expr Purif] 2015 Apr; Vol. 108, pp. 9-12. Date of Electronic Publication: 2015 Jan 05.
DOI: 10.1016/j.pep.2014.12.017
Abstrakt: Periplasmic localization of recombinant proteins offers advantages over cytoplasmic protein expression. In this study signal sequence of amicyanin, which is encoded by the mauC gene of Paracoccus denitrificans, was used to express the light chain variable domain of the human κIO8/O18 germline antibody in the periplasm of Escherichiacoli. The expressed protein was purified in good yield (70mg/L of culture) in one step from the periplasmic fraction by affinity chromatography using an engineered hexahistidine tag. Circular dichroism spectroscopy was used to determine if the secondary and tertiary structures of the protein and its thermal stability corresponded to those of the native folded protein. The expressed and purified protein was indeed properly folded and exhibited a reasonable thermal transition temperature of 53°C. These results indicate that the amicyanin signal sequence may be particularly useful for prokaryotic expression of proteins which are prone to mis-folding, aggregation or formation of inclusion bodies, all of which were circumvented in this study.
(Copyright © 2014 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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