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Expanding the Scope of Ribosome-Mediated Biosynthesis in vitro using tRNA-Aminoacylating Ribozyme
被引:2
|作者:
Cho, Namjin
[1
]
Jin, Haneul
[1
]
Jeon, Hyewon
[1
]
Lee, Kanghun
[2
]
Lee, Joongoo
[1
,2
]
机构:
[1] Pohang Univ Sci & Technol POSTECH, Dept Chem Engn, Pohang 37673, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Sch Interdisciplinary Biosci & Bioengn I Bio, Pohang 37673, South Korea
基金:
新加坡国家研究基金会;
关键词:
cell-free system;
cyclic backbone;
non-canonical substrate;
ribosome;
ribozyme;
synthetic biology;
UNNATURAL AMINO-ACIDS;
PI-PI INTERACTIONS;
GENETIC-CODE;
CHEMICAL AMINOACYLATION;
MACROCYCLIC PEPTIDES;
TRANSLATION SYSTEM;
PROTEIN;
SELECTION;
SUBSTITUTION;
RECOGNITION;
D O I:
10.1002/ijch.202300174
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Proteins are synthesized within ribosomes through the polymerization of amino acids (AAs). This process requires prior activation of AAs through aminoacylation that attaches them to their corresponding transfer RNAs (tRNAs). Within cells, this attachment is facilitated by aminoacyl-tRNA synthetase, resulting in a tRNA:AA conjugate. A set of ribozymes developed to acylate tRNA with non-canonical substrates enables this process outside the confines of living cells, thereby facilitating the synthesis of novel bio-based products. In modern biotechnology, aminoacylating ribozymes contribute to the production of innovative bio-based materials bearing functional non-canonical chemical substrates (NCSs) and fill the gaps in synthesizing unique polymeric backbones, extending the scope beyond traditional peptide bonds. This review summarizes current understanding of flexizymes at the molecular level and their application in generating exceptional polymeric backbones through ribosome-mediated synthesis in vitro.
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页数:13
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