Efficient In Vitro Full‐Sense‐Codons Protein Synthesis. Issue 10 (8th June 2022)
- Record Type:
- Journal Article
- Title:
- Efficient In Vitro Full‐Sense‐Codons Protein Synthesis. Issue 10 (8th June 2022)
- Main Title:
- Efficient In Vitro Full‐Sense‐Codons Protein Synthesis
- Authors:
- Wu, Yang
Tang, Mengtong
Wang, Zhaoguan
Yang, Youhui
Li, Zhong
Liang, Shurui
Yin, Peng
Qi, Hao - Abstract:
- Abstract: Termination of translation is essential but hinders applications of genetic code engineering, e.g., unnatural amino acids incorporation and codon randomization mediated saturation mutagenesis. Here, for the first time, it is demonstrated that E. coli Pth and ArfB together play an efficient translation termination without codon preference in the absence of class‐I release factors. By degradation of the targeted protein, both essential and alternative termination types of machinery are completely removed to disable codon‐dependent termination in cell extract. Moreover, a total of 153 engineered tRNAs are screened for efficient all stop‐codons decoding to construct a codon‐dependent termination defect in vitro protein synthesis with all 64 sense‐codons, iPSSC. Finally, this full sense genetic code achieves significant improvement in the incorporation of distinct unnatural amino acids at up to 12 positions and synthesis of protein encoding consecutive NNN codons. By decoding all information in nucleotides to amino acids, iPSSC may hold great potential in building artificial protein synthesis beyond the cell. Abstract : Global translation termination is identified and completely removed with deletion of one set of essential factors, RF1, RF2, SsrA, ArfA, ArfB, and Pth, to achieve in vitro protein synthesis with 64 sense codons (iPSSC), which is capable of transferring all information in nucleotide to amino acids. iPSSC builds a versatile platform with all‐sense geneticAbstract: Termination of translation is essential but hinders applications of genetic code engineering, e.g., unnatural amino acids incorporation and codon randomization mediated saturation mutagenesis. Here, for the first time, it is demonstrated that E. coli Pth and ArfB together play an efficient translation termination without codon preference in the absence of class‐I release factors. By degradation of the targeted protein, both essential and alternative termination types of machinery are completely removed to disable codon‐dependent termination in cell extract. Moreover, a total of 153 engineered tRNAs are screened for efficient all stop‐codons decoding to construct a codon‐dependent termination defect in vitro protein synthesis with all 64 sense‐codons, iPSSC. Finally, this full sense genetic code achieves significant improvement in the incorporation of distinct unnatural amino acids at up to 12 positions and synthesis of protein encoding consecutive NNN codons. By decoding all information in nucleotides to amino acids, iPSSC may hold great potential in building artificial protein synthesis beyond the cell. Abstract : Global translation termination is identified and completely removed with deletion of one set of essential factors, RF1, RF2, SsrA, ArfA, ArfB, and Pth, to achieve in vitro protein synthesis with 64 sense codons (iPSSC), which is capable of transferring all information in nucleotide to amino acids. iPSSC builds a versatile platform with all‐sense genetic code for artificial protein engineering. … (more)
- Is Part Of:
- Advanced biology. Volume 6:Issue 10(2022)
- Journal:
- Advanced biology
- Issue:
- Volume 6:Issue 10(2022)
- Issue Display:
- Volume 6, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 6
- Issue:
- 10
- Issue Sort Value:
- 2022-0006-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-06-08
- Subjects:
- codon reassignment -- protein degradation -- synthetic biology -- translation termination
Molecular biology -- Periodicals
Systems biology -- Periodicals
Biological systems -- Periodicals
Biotechnology -- Periodicals
Bioengineering -- Periodicals
Biomedical engineering -- Periodicals
660.6 - Journal URLs:
- https://onlinelibrary.wiley.com/journal/27010198 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adbi.202200023 ↗
- Languages:
- English
- ISSNs:
- 2701-0198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24155.xml