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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:
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.
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页码:1433 / 1440
页数:8
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