Putting amino acids onto tRNAs: The aminoacyl-tRNA synthetases as catalysts
- PMID: 33837710
- DOI: 10.1016/bs.enz.2020.06.003
Putting amino acids onto tRNAs: The aminoacyl-tRNA synthetases as catalysts
Abstract
In this chapter we consider the catalytic approaches used by aminoacyl-tRNA synthetase (AARS) enzymes to synthesize aminoacyl-tRNA from cognate amino acid and tRNA. This ligase reaction proceeds through an activated aminoacyl-adenylate (aa-AMP). Common themes among AARSs include use of induced fit to drive catalysis and transition state stabilization by class-conserved sequence and structure motifs. Active site metal ions contribute to the amino acid activation step, while amino acid transfer to tRNA is generally a substrate-assisted concerted mechanism. A distinction between classes is the rate-limiting step for aminoacylation. We present some examples for each aspect of aminoacylation catalysis, including the experimental approaches developed to address questions of AARS chemistry.
Keywords: Aminoacyl-tRNA synthetase; Catalysis; Concerted; Divalent metals; Dynamics; Enzyme mechanisms; Induced fit; Nucleophile; Rate-limiting step; Substrate-assisted; Transition state; tRNA.
© 2020 Elsevier Inc. All rights reserved.
Similar articles
-
Relationship of the CCA sequence of tRNA with the early evolutional aspect of aminoacyl-tRNA synthetases.Nucleic Acids Symp Ser. 1999;(42):211-2. doi: 10.1093/nass/42.1.211. Nucleic Acids Symp Ser. 1999. PMID: 10780454
-
Trans-editing by aminoacyl-tRNA synthetase-like editing domains.Enzymes. 2020;48:69-115. doi: 10.1016/bs.enz.2020.07.002. Epub 2020 Sep 8. Enzymes. 2020. PMID: 33837712 Review.
-
Noncanonical inputs and outputs of tRNA aminoacylation.Enzymes. 2020;48:117-147. doi: 10.1016/bs.enz.2020.04.003. Epub 2020 Jun 12. Enzymes. 2020. PMID: 33837702
-
A continuous assay for monitoring the synthetic and proofreading activities of multiple aminoacyl-tRNA synthetases for high-throughput drug discovery.RNA Biol. 2018;15(4-5):659-666. doi: 10.1080/15476286.2017.1397262. Epub 2017 Dec 15. RNA Biol. 2018. PMID: 29168435 Free PMC article.
-
Synthetic and editing reactions of aminoacyl-tRNA synthetases using cognate and non-cognate amino acid substrates.Methods. 2017 Jan 15;113:13-26. doi: 10.1016/j.ymeth.2016.09.015. Epub 2016 Oct 3. Methods. 2017. PMID: 27713080 Review.
Cited by
-
Reflections on the Origin of Coded Protein Biosynthesis.Biomolecules. 2024 Apr 25;14(5):518. doi: 10.3390/biom14050518. Biomolecules. 2024. PMID: 38785925 Free PMC article. Review.
-
Natural human tRNAAla anticodon variants mistranslate the genetic code.RNA. 2025 May 16;31(6):791-806. doi: 10.1261/rna.080450.125. RNA. 2025. PMID: 40118510
MeSH terms
Substances
LinkOut - more resources
Miscellaneous