Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region
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Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region. / Goltermann, Lise; Borch Jensen, Martin; Bentin, Thomas.
In: Protein Engineering Design and Selection (Print Edition), Vol. 24, No. 1-2, 01.2011, p. 125-129.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region
AU - Goltermann, Lise
AU - Borch Jensen, Martin
AU - Bentin, Thomas
PY - 2011/1
Y1 - 2011/1
N2 - In bacteria, the 5' mRNA coding region plays an important role in determining translation output. Here, we report synthetic sequences that when placed in the 5'-mRNA coding region, leading to recombinant proteins containing short N-terminal extensions, virtually abolish, enhance or produce intermediate expression levels of green fluorescent protein in Escherichia coli. At least in one case, no apparent effect on protein stability was observed, pointing to RNA level effects as the principal reason for the observed expression differences. Targeting a synonymous codon library to the 5' coding sequence allowed tuning of protein expression over ~300-fold with preservation of amino acid identity. This approach is simple and should be generally applicable in bacteria. The data support that features in the 5' mRNA coding region near the AUG start codon are key in determining translation output and hence is important to recombinant and, most certainly, endogenous gene expression.
AB - In bacteria, the 5' mRNA coding region plays an important role in determining translation output. Here, we report synthetic sequences that when placed in the 5'-mRNA coding region, leading to recombinant proteins containing short N-terminal extensions, virtually abolish, enhance or produce intermediate expression levels of green fluorescent protein in Escherichia coli. At least in one case, no apparent effect on protein stability was observed, pointing to RNA level effects as the principal reason for the observed expression differences. Targeting a synonymous codon library to the 5' coding sequence allowed tuning of protein expression over ~300-fold with preservation of amino acid identity. This approach is simple and should be generally applicable in bacteria. The data support that features in the 5' mRNA coding region near the AUG start codon are key in determining translation output and hence is important to recombinant and, most certainly, endogenous gene expression.
U2 - 10.1093/protein/gzq086
DO - 10.1093/protein/gzq086
M3 - Journal article
C2 - 21047874
VL - 24
SP - 125
EP - 129
JO - Protein Engineering, Design and Selection
JF - Protein Engineering, Design and Selection
SN - 1741-0126
IS - 1-2
ER -
ID: 23253414