Back to Search
Start Over
Synthesis of tRNA analogues containing a terminal ribose locked in the South conformation to study tRNA-dependent enzymes.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2018 Mar 14; Vol. 16 (11), pp. 1903-1911. - Publication Year :
- 2018
-
Abstract
- We report here the synthetic route of two constrained dinucleotides and the determination of the sugar puckering by NMR analyses of the starting nucleosides. Enzymatic ligation to microhelix-RNAs provide access to tRNA analogues containing a 3' terminal A <superscript>76</superscript> locked in South conformation. Biological evaluation of our tRNA analogues has been performed using amino-acyl tRNA-dependent transferase FemX <subscript>Wv</subscript> , which mediates non-ribosomal incorporation of amino acids into the bacterial cell wall. We have shown that our tRNA analogues inhibited the aminoacyl transfer reaction catalyzed by FemX <subscript>Wv</subscript> with IC <subscript>50s</subscript> of 10 and 8 μM. These results indicate that FemX <subscript>Wv</subscript> displays a moderate preference for tRNAs containing a terminal A <superscript>76</superscript> locked in the South conformation and that a South to North switch in the conformation of the terminal ribose might contribute to the release of the uncharged tRNA <superscript>Ala</superscript> product of the aminoacyl transfer reaction catalyzed by FemX <subscript>wv</subscript> .
- Subjects :
- Aminoacyltransferases antagonists & inhibitors
Aminoacyltransferases metabolism
Bacterial Proteins metabolism
Models, Molecular
Nucleic Acid Conformation
RNA, Transfer chemical synthesis
RNA, Transfer metabolism
Ribonucleotides chemical synthesis
Ribonucleotides metabolism
Ribose chemical synthesis
Ribose metabolism
Weissella enzymology
Weissella metabolism
Chemistry Techniques, Synthetic methods
RNA, Transfer chemistry
Ribonucleotides chemistry
Ribose analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1477-0539
- Volume :
- 16
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29484333
- Full Text :
- https://doi.org/10.1039/c8ob00019k