Reference: Chen B, et al. (2024) The mechanism of discriminative aminoacylation by isoleucyl-tRNA synthetase based on wobble nucleotide recognition. Nat Commun 15(1): 10817.

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Abstract


The faithful charging of amino acids to cognate tRNAs by aminoacyl-tRNA synthetases (AARSs) determines the fidelity of protein translation. Isoleucyl-tRNA synthetase (IleRS) distinguishes tRNA(Ile) from tRNA(Met) solely based on the nucleotide at wobble position (N34), and a single substitution at N34 could exchange the aminoacylation specificity between two tRNAs. Here, we report the structural and biochemical mechanism of N34 recognition-based tRNA discrimination by Saccharomyces cerevisiae IleRS (ScIleRS). ScIleRS utilizes a eukaryotic/archaeal-specific arginine as the H-bond donor to recognize the common carbonyl group (H-bond acceptor) of various N34s of tRNA(Ile), which induces mutual structural adaptations between ScIleRS and tRNA(Ile) to achieve a preferable editing state. C34 of unmodified tRNA(Ile)(CAU) (behaves like tRNA(Met)) lacks a relevant H-bond acceptor, which disrupts key H-bonding interactions and structural adaptations and suspends the ScIleRS.tRNA(Ile)(CAU) complex in an initial non-reactive state. This wobble nucleotide recognition-based structural adaptation provides mechanistic insights into selective tRNA aminoacylation by AARSs.

Reference Type
Journal Article
Authors
Chen B, Yi F, Luo Z, Lu F, Liu H, Luo S, Gu Q, Zhou H
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