Molecular basis of tRNA aminocarboxypropyl-transferase TapT for substrate recognition

3-(3-amino-3-carboxypropyl) uridine (acp3U) is a highly conserved modification found in variable- and D-loops of transfer RNAs (tRNAs) in bacteria and eukarya. TapT has been identified as the enzyme responsible for acp3U modification at position 47 of Escherichia coli tRNAs in the presence of S-adenosylmethionine (SAM), while the specific substrate binding details and catalytic mechanism of TapT remain unknown. Here, we determined the three-dimensional structure of TapT in a SAM-bound state. The overall structure adopts SPOUT folding, with SAM located in an adaptive pocket. The cofactor recognition mode was further evaluated by additional structures of S-methyl-5'-thioadenosine or sinefungin to TapT, together with isothermal titration calorimetry to explore binding affinity and liquid chromatography-mass spectrometry experiments to detect enzymatic activity. Furthermore, we performed fluorescence polarization assays to explore the tRNA recognition mechanism of TapT. It thus provides a thorough molecular basis for TapT substrate recognition and may promote further application in biochemistry, molecular biology, and tumor diagnostics.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-11-13
DOI
https://doi.org/10.1093/nar/gkaf1202
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Molecular basis of tRNA aminocarboxypropyl-transferase TapT for substrate recognition

Yao Jiang, Gong‐Li Tang, Hengrui Liang, Hai‐Xue Pan et al.
Nucleic Acids Research
RNA modifications and cancer
article

Molecular basis of tRNA aminocarboxypropyl-transferase TapT for substrate recognition

Yao Jiang, Gong‐Li Tang, Hengrui Liang, Hai‐Xue Pan, Pingwei Liu, Jinyue Pu, Zhe Wang, Weiyan Wang, Yan Wu, Aiai Sun
article en

Abstract

3-(3-amino-3-carboxypropyl) uridine (acp3U) is a highly conserved modification found in variable- and D-loops of transfer RNAs (tRNAs) in bacteria and eukarya. TapT has been identified as the enzyme responsible for acp3U modification at position 47 of Escherichia coli tRNAs in the presence of S-adenosylmethionine (SAM), while the specific substrate binding details and catalytic mechanism of TapT remain unknown. Here, we determined the three-dimensional structure of TapT in a SAM-bound state. The overall structure adopts SPOUT folding, with SAM located in an adaptive pocket. The cofactor recognition mode was further evaluated by additional structures of S-methyl-5'-thioadenosine or sinefungin to TapT, together with isothermal titration calorimetry to explore binding affinity and liquid chromatography-mass spectrometry experiments to detect enzymatic activity. Furthermore, we performed fluorescence polarization assays to explore the tRNA recognition mechanism of TapT. It thus provides a thorough molecular basis for TapT substrate recognition and may promote further application in biochemistry, molecular biology, and tumor diagnostics.

Nucleic Acids ResearchVol. 53(21)
Anhui Medical University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), ZheJiang Academy of Agricultural Sciences (CN), First Affiliated Hospital of Anhui Medical University (CN), University of Chinese Academy of Sciences (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, University of Science and Technology of China, University of Chinese Academy of Sciences
Openalex Percentile: Top 69%
RNA modifications and cancer
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