Literature DB >> 22362707

Glycine to glutamic acid misincorporation observed in a recombinant protein expressed by Escherichia coli cells.

Yunping Huang1, Brian O'Mara, Matthew Conover, Richard Ludwig, Jinmei Fu, Li Tao, Zheng Jian Li, Siegfried Rieble, Michael J Grace, Reb J Russell.   

Abstract

A novel amino acid misincorporation, in which the intended glycine (Gly) residues were replaced by a glutamic acid (Glu), was observed in a recombinant protein expressed by Escherichia coli. The misincorporation was identified by peptide mapping and liquid chromatography-tandem mass spectrometric analysis on proteolyzed peptides of the protein and verified using the corresponding synthetic peptides containing the misincorporated residues. Analysis of the distribution of the misincorporated residues and their codon usage shows strong correlation between this misincorporation and the use of rarely used codon within the E. coli expression system. Results in this study suggest that the usage of the rare codon GGA has resulted in a Glu for Gly misincorporation.
Copyright © 2012 The Protein Society.

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Year:  2012        PMID: 22362707      PMCID: PMC3403460          DOI: 10.1002/pro.2046

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


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