Protein Synthesis in Coupled and Uncoupled Cell-Free Prokaryotic Gene Expression Systems

被引:16
作者
Hansen, Maike M. K. [1 ]
Rosquelles, Marta Ventosa [1 ]
Yelleswarapu, Maaruthy [1 ]
Maas, Roel J. M. [1 ]
van Vugt-Jonker, Aafke J. [1 ]
Heus, Hans A. [1 ]
Huck, Wilhelm T. S. [1 ]
机构
[1] Radboud Univ Nijmegen, Inst Mol & Mat, Heyendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands
来源
ACS SYNTHETIC BIOLOGY | 2016年 / 5卷 / 12期
基金
欧洲研究理事会;
关键词
uncoupling; cell-free; ribosomes; transcription; translation; DNA TOPOISOMERASE-I; ESCHERICHIA-COLI; TRANSLATIONAL EFFICIENCY; QUANTITATIVE-ANALYSIS; SECONDARY STRUCTURE; ACTIVE PROTEINS; RNA-POLYMERASE; TRANSCRIPTION; RIBOSOME; BINDING;
D O I
10.1021/acssynbio.6b00010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Secondary structure formation of mRNA, caused by desynchronization of transcription and translation, is known to impact gene expression in vivo. Yet, inactivation of mRNA by secondary structures in cell-free protein expression is frequently overlooked. Transcription and translation rates are often not highly synchronized in cell-free expression systems, leading to a temporal mismatch between the processes and a drop in efficiency of protein production. By devising a cell-free gene expression platform in which transcriptional and translational elongation are successfully performed independently, we determine that sequence-dependent mRNA secondary structures are the main cause of mRNA inactivation in in vitro gene expression.
引用
收藏
页码:1433 / 1440
页数:8
相关论文
共 40 条
  • [1] Pausing by bacterial RNA polymerase is mediated by mechanistically distinct classes of signals
    Artsimovitch, I
    Landick, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) : 7090 - 7095
  • [2] BARANOV VI, 1993, METHOD ENZYMOL, V217, P123
  • [3] Translation rate is controlled by coupled trade-offs between site accessibility, selective RNA unfolding and sliding at upstream standby sites
    Borujeni, Amin Espah
    Channarasappa, Anirudh S.
    Salis, Howard M.
    [J]. NUCLEIC ACIDS RESEARCH, 2014, 42 (04) : 2646 - 2659
  • [4] The Native 3D Organization of Bacterial Polysomes
    Brandt, Florian
    Etchells, Stephanie A.
    Ortiz, Julio O.
    Elcock, Adrian H.
    Hartl, F. Ulrich
    Baumeister, Wolfgang
    [J]. CELL, 2009, 136 (02) : 261 - 271
  • [5] Brophy JAN, 2014, NAT METHODS, V11, P508, DOI [10.1038/NMETH.2926, 10.1038/nmeth.2926]
  • [6] Gene Position More Strongly Influences Cell-Free Protein Expression from Operons than T7 Transcriptional Promoter Strength
    Chizzolini, Fabio
    Forlin, Michele
    Cecchi, Dario
    Mansy, Sheref S.
    [J]. ACS SYNTHETIC BIOLOGY, 2014, 3 (06): : 363 - 371
  • [7] An in vitro Autogene
    Davidson, Eric A.
    Meyer, Adam J.
    Ellefson, Jared W.
    Levy, Matthew
    Ellington, Andrew D.
    [J]. ACS SYNTHETIC BIOLOGY, 2012, 1 (05): : 190 - 196
  • [8] Lost in translation: the influence of ribosomes on bacterial mRNA decay
    Deana, A
    Belasco, JG
    [J]. GENES & DEVELOPMENT, 2005, 19 (21) : 2526 - 2533
  • [9] CONTROL OF TRANSLATION BY MESSENGER-RNA SECONDARY STRUCTURE IN ESCHERICHIA-COLI - A QUANTITATIVE-ANALYSIS OF LITERATURE DATA
    DESMIT, MH
    VANDUIN, J
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1994, 244 (02) : 144 - 150
  • [10] SECONDARY STRUCTURE OF THE RIBOSOME BINDING-SITE DETERMINES TRANSLATIONAL EFFICIENCY - A QUANTITATIVE-ANALYSIS
    DESMIT, MH
    VANDUIN, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) : 7668 - 7672