The contemporary aminoacyl-tRNA synthetases (aaRSs) are highly specific toward cognitive amino acids and tRNAs, because the fidelity of translation from genetic code to proteins relies mainly upon the accurate aminoacylation of tRNAs. Consequently, the mechanism of their recognition events is extremely complex, which has made it difficult to engineer the aaRSs with desired specificities. The central goal of this proposal is to devise a novel and practical catalytic system composed of catalytic RNA molecules (ribozymes) for the synthesis of natural and non-natural aminoacyl-tRNAs. We have recently succeeded in generating a novel ribozyme capable of synthesizing aminoacyl-tRNA. This ribozyme, referred to as ARS ribozyme (aminoacyl-tRNA synthetase ribozyme), is able to specifically recognize a glutamine cyanomethyl ester and charge the glutaminyl group on a tRNA molecule. In this proposal, we will plan to systematically evolve the ARS ribozyme into highly selective and efficient ARS ribozymes for the synthesis of various aminoacyl-tRNAs. Our ribozyme-based catalytic system will potentially offer a simple and facile method for the synthesis of aminoacyl-tRNAs in vitro. The results from these experiments will be used to drive future direction of our long-term goal, a cell-free in vitro translation system composed of ARS ribozymes, which facilitates the site-specific incorporation of non-natural amino acids into proteins. Our experiments may also provide new evidence to support an RNA-based translation system postulated in the context of the RNA world hypothesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM059159-03
Application #
6498734
Study Section
Physiological Chemistry Study Section (PC)
Program Officer
Rhoades, Marcus M
Project Start
2000-02-01
Project End
2004-01-31
Budget Start
2002-02-01
Budget End
2003-01-31
Support Year
3
Fiscal Year
2002
Total Cost
$181,695
Indirect Cost
Name
State University of New York at Buffalo
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
Ohta, Atsushi; Yamagishi, Yusuke; Suga, Hiroaki (2008) Synthesis of biopolymers using genetic code reprogramming. Curr Opin Chem Biol 12:159-67
Kang, Taek Jin; Suga, Hiroaki (2008) Ribosomal synthesis of nonstandard peptides. Biochem Cell Biol 86:92-9
Ohta, Atsushi; Murakami, Hiroshi; Higashimura, Eri et al. (2007) Synthesis of polyester by means of genetic code reprogramming. Chem Biol 14:1315-22
Ohuchi, Masaki; Murakami, Hiroshi; Suga, Hiroaki (2007) The flexizyme system: a highly flexible tRNA aminoacylation tool for the translation apparatus. Curr Opin Chem Biol 11:537-42
Kang, Taek Jin; Suga, Hiroaki (2007) In vitro selection of a 5'-purine ribonucleotide transferase ribozyme. Nucleic Acids Res 35:4186-94
Murakami, Hiroshi; Ohta, Atsushi; Ashigai, Hiroshi et al. (2006) A highly flexible tRNA acylation method for non-natural polypeptide synthesis. Nat Methods 3:357-9
Hodgson, David R W; Suga, Hiroaki (2004) Mechanistic studies on acyl-transferase ribozymes and beyond. Biopolymers 73:130-50
Murakami, Hiroshi; Saito, Hirohide; Suga, Hiroaki (2003) A versatile tRNA aminoacylation catalyst based on RNA. Chem Biol 10:655-62
Saito, Hirohide; Suga, Hiroaki (2002) Outersphere and innersphere coordinated metal ions in an aminoacyl-tRNA synthetase ribozyme. Nucleic Acids Res 30:5151-9
Murakami, Hiroshi; Bonzagni, Neil J; Suga, Hiroaki (2002) Aminoacyl-tRNA synthesis by a resin-immobilized ribozyme. J Am Chem Soc 124:6834-5

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