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
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