Unknown

Dataset Information

0

Flexizyme-catalyzed synthesis of 3'-aminoacyl-NH-tRNAs.


ABSTRACT: Structural analysis of ribosomes in complex with aminoacyl- and/or peptidyl-transfer RNA (tRNA) often suffers from rapid hydrolysis of the ester bond of aminoacyl-tRNAs. To avoid this issue, several methods to introduce an unhydrolyzable amide bond instead of the canonical ester bond have been developed to date. However, the existing methodologies require rather complex steps of synthesis and are often inapplicable to a variety of amino acids including those with noncanonical structures. Here, we report a new method to synthesize 3'-aminoacyl-NH-tRNAs by means of flexizymes-ribozymes capable of charging amino acids onto tRNAs. We show that two types of flexizymes, dFx and eFx, are able to charge various amino acids, including nonproteinogenic ones, onto tRNA or microhelix RNA bearing the 3'-deoxy-3'-amino-adenosine. Due to the versatility of the flexizymes toward any pair of nonproteinogenic amino acids and full-length or fragment tRNAs, this method provides researchers an opportunity to use a wide array of hydrolytically stable 3'-aminoacyl-NH-tRNAs and analogs for various studies.

SUBMITTER: Katoh T 

PROVIDER: S-EPMC6511858 | biostudies-other | 2019 May

REPOSITORIES: biostudies-other

altmetric image

Publications

Flexizyme-catalyzed synthesis of 3'-aminoacyl-NH-tRNAs.

Katoh Takayuki T   Suga Hiroaki H  

Nucleic acids research 20190501 9


Structural analysis of ribosomes in complex with aminoacyl- and/or peptidyl-transfer RNA (tRNA) often suffers from rapid hydrolysis of the ester bond of aminoacyl-tRNAs. To avoid this issue, several methods to introduce an unhydrolyzable amide bond instead of the canonical ester bond have been developed to date. However, the existing methodologies require rather complex steps of synthesis and are often inapplicable to a variety of amino acids including those with noncanonical structures. Here, w  ...[more]

Similar Datasets

| S-EPMC2682858 | biostudies-literature
| S-EPMC7367177 | biostudies-literature
| S-EPMC4005694 | biostudies-literature
| S-EPMC4992060 | biostudies-literature
| S-EPMC8565323 | biostudies-literature
| S-EPMC7196831 | biostudies-literature
| S-EPMC4534242 | biostudies-other
| S-EPMC9291533 | biostudies-literature
2020-03-26 | GSE126384 | GEO
| S-EPMC3592460 | biostudies-literature