Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region

Research output: Contribution to journalJournal articleResearchpeer-review

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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 journalJournal articleResearchpeer-review

Harvard

Goltermann, L, Borch Jensen, M & Bentin, T 2011, 'Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region', Protein Engineering Design and Selection (Print Edition), vol. 24, no. 1-2, pp. 125-129. https://doi.org/10.1093/protein/gzq086

APA

Goltermann, L., Borch Jensen, M., & Bentin, T. (2011). Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region. Protein Engineering Design and Selection (Print Edition), 24(1-2), 125-129. https://doi.org/10.1093/protein/gzq086

Vancouver

Goltermann L, Borch Jensen M, Bentin T. Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region. Protein Engineering Design and Selection (Print Edition). 2011 Jan;24(1-2):125-129. https://doi.org/10.1093/protein/gzq086

Author

Goltermann, Lise ; Borch Jensen, Martin ; Bentin, Thomas. / Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region. In: Protein Engineering Design and Selection (Print Edition). 2011 ; Vol. 24, No. 1-2. pp. 125-129.

Bibtex

@article{31b2d2b0f3b411dfb6d2000ea68e967b,
title = "Tuning protein expression using synonymous codon libraries targeted to the 5' mRNA coding region",
abstract = "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.",
author = "Lise Goltermann and {Borch Jensen}, Martin and Thomas Bentin",
year = "2011",
month = jan,
doi = "10.1093/protein/gzq086",
language = "English",
volume = "24",
pages = "125--129",
journal = "Protein Engineering, Design and Selection",
issn = "1741-0126",
publisher = "Oxford University Press",
number = "1-2",

}

RIS

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