Expanding the eukaryotic genetic code with a biosynthesized 21st amino acid. (28th September 2022)
- Record Type:
- Journal Article
- Title:
- Expanding the eukaryotic genetic code with a biosynthesized 21st amino acid. (28th September 2022)
- Main Title:
- Expanding the eukaryotic genetic code with a biosynthesized 21st amino acid
- Authors:
- Wu, Kuan‐Lin
Moore, Joshua A.
Miller, Mitchell D.
Chen, Yuda
Lee, Catherine
Xu, Weijun
Peng, Zane
Duan, Qinghui
Phillips, George N.
Uribe, Rosa A.
Xiao, Han - Abstract:
- Abstract: Genetic code expansion technology allows for the use of noncanonical amino acids (ncAAs) to create semisynthetic organisms for both biochemical and biomedical applications. However, exogenous feeding of chemically synthesized ncAAs at high concentrations is required to compensate for the inefficient cellular uptake and incorporation of these components into proteins, especially in the case of eukaryotic cells and multicellular organisms. To generate organisms capable of autonomously biosynthesizing an ncAA and incorporating it into proteins, we have engineered a metabolic pathway for the synthesis of O ‐methyltyrosine (OMeY). Specifically, we endowed organisms with a marformycins biosynthetic pathway‐derived methyltransferase that efficiently converts tyrosine to OMeY in the presence of the co‐factor S ‐adenosylmethionine. The resulting cells can produce and site‐specifically incorporate OMeY into proteins at much higher levels than cells exogenously fed OMeY. To understand the structural basis for the substrate selectivity of the transferase, we solved the X‐ray crystal structures of the ligand‐free and tyrosine‐bound enzymes. Most importantly, we have extended this OMeY biosynthetic system to both mammalian cells and the zebrafish model to enhance the utility of genetic code expansion. The creation of autonomous eukaryotes using a 21st amino acid will make genetic code expansion technology more applicable to multicellular organisms, providing valuable vertebrateAbstract: Genetic code expansion technology allows for the use of noncanonical amino acids (ncAAs) to create semisynthetic organisms for both biochemical and biomedical applications. However, exogenous feeding of chemically synthesized ncAAs at high concentrations is required to compensate for the inefficient cellular uptake and incorporation of these components into proteins, especially in the case of eukaryotic cells and multicellular organisms. To generate organisms capable of autonomously biosynthesizing an ncAA and incorporating it into proteins, we have engineered a metabolic pathway for the synthesis of O ‐methyltyrosine (OMeY). Specifically, we endowed organisms with a marformycins biosynthetic pathway‐derived methyltransferase that efficiently converts tyrosine to OMeY in the presence of the co‐factor S ‐adenosylmethionine. The resulting cells can produce and site‐specifically incorporate OMeY into proteins at much higher levels than cells exogenously fed OMeY. To understand the structural basis for the substrate selectivity of the transferase, we solved the X‐ray crystal structures of the ligand‐free and tyrosine‐bound enzymes. Most importantly, we have extended this OMeY biosynthetic system to both mammalian cells and the zebrafish model to enhance the utility of genetic code expansion. The creation of autonomous eukaryotes using a 21st amino acid will make genetic code expansion technology more applicable to multicellular organisms, providing valuable vertebrate models for biological and biomedical research. Abstract : PDB Code(s): 7UX6, 7UX7 and 7UX8 ; … (more)
- Is Part Of:
- Protein science. Volume 31:Number 10(2022)
- Journal:
- Protein science
- Issue:
- Volume 31:Number 10(2022)
- Issue Display:
- Volume 31, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 31
- Issue:
- 10
- Issue Sort Value:
- 2022-0031-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-09-28
- Subjects:
- biosynthesis -- cell engineering -- genetic code expansion -- metabolic engineering -- noncanonical amino acid -- site‐specific incorporation -- unnatural amino acid
Proteins -- Periodicals
572.6 - Journal URLs:
- http://www.proteinscience.org/ ↗
http://www3.interscience.wiley.com/journal/121502357/ ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1002/pro.4443 ↗
- Languages:
- English
- ISSNs:
- 0961-8368
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.105500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24062.xml