Structural Basis and Rational Design of Nucleotide Analogue Inhibitor Evading the SARS-CoV-2 Proofreading Enzyme

All coronaviruses (CoVs) encode an exoribonuclease in nonstructural protein nsp14 (nsp14 ExoN), which is required for the excision of mismatched nucleotides or nucleotide analogues (NAs) that are incorporated into nascent RNA. Here, we investigated the mechanism by which NAs evade SARS-CoV-2 nsp14 ExoN cleavage using chemically synthesized RNA with NAs incorporated at the 3' end. Nsp14 ExoN exhibited significantly attenuated activity on RNA with sofosbuvir monophosphate (SMP) compared with natural nucleotides, remdesivir/molnupiravir monophosphate, and, in particular, AT-9010 monophosphate (ATMP), which has the same chemically modified ribose moiety as SMP, incorporated at the 3' end. Cryo-electron microscopy structures of nsp10/14 bound to RNA-SMP/-ATMP and mutagenesis studies revealed the essential roles of H95/Q145/F146 in recognizing the base moiety and thus pulling the NAs into a favored conformation for cleavage. Therefore, NAs may evade nsp14 ExoN cleavage by having (1) a base that does not interact with H95, Q145, or F146 and (2) a chemically modified ribose. Guided by this hypothesis, two NAs were designed to effectively resist nsp14 ExoN cleavage. These results inform the rational design of anti-CoV NAs.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-06-13
DOI
https://doi.org/10.1021/jacs.5c05014
Citations
3
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
4.19

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article

Structural Basis and Rational Design of Nucleotide Analogue Inhibitor Evading the SARS-CoV-2 Proofreading Enzyme

Xiaoyu Chang, Yuanchen Dong, Liming Yan, Feng Zhou et al.
3 citations
Journal of the American Chemical Society
SARS-CoV-2 and COVID-19 Research
4.19
article

Structural Basis and Rational Design of Nucleotide Analogue Inhibitor Evading the SARS-CoV-2 Proofreading Enzyme

Xiaoyu Chang, Yuanchen Dong, Liming Yan, Feng Zhou, Zihe Rao, Yufan Pan, Zhiyong Lou, Yucen Huang, Dongsheng Liu, Jin Ge, Bo Huang, Junbo Wang, Yixiao Liu, Lejin Zhang
article en
3 citations

Abstract

All coronaviruses (CoVs) encode an exoribonuclease in nonstructural protein nsp14 (nsp14 ExoN), which is required for the excision of mismatched nucleotides or nucleotide analogues (NAs) that are incorporated into nascent RNA. Here, we investigated the mechanism by which NAs evade SARS-CoV-2 nsp14 ExoN cleavage using chemically synthesized RNA with NAs incorporated at the 3' end. Nsp14 ExoN exhibited significantly attenuated activity on RNA with sofosbuvir monophosphate (SMP) compared with natural nucleotides, remdesivir/molnupiravir monophosphate, and, in particular, AT-9010 monophosphate (ATMP), which has the same chemically modified ribose moiety as SMP, incorporated at the 3' end. Cryo-electron microscopy structures of nsp10/14 bound to RNA-SMP/-ATMP and mutagenesis studies revealed the essential roles of H95/Q145/F146 in recognizing the base moiety and thus pulling the NAs into a favored conformation for cleavage. Therefore, NAs may evade nsp14 ExoN cleavage by having (1) a base that does not interact with H95, Q145, or F146 and (2) a chemically modified ribose. Guided by this hypothesis, two NAs were designed to effectively resist nsp14 ExoN cleavage. These results inform the rational design of anti-CoV NAs.

Journal of the American Chemical SocietyVol. 147(25)
University of Science and Technology of China (CN), Hong Kong Polytechnic University (HK), Chinese Academy of Sciences (CN), Nankai University (CN), ShanghaiTech University (CN), Zhengzhou University (CN), Czech Academy of Sciences, Institute of Biophysics (CZ), Beijing Enterprises (China) (CN), Institute of Biophysics (CN), Institute of Chemistry (CN), State Key Laboratory of Chemical Engineering (CN), University of Chinese Academy of Sciences (CN), State Key Laboratory of Medicinal Chemical Biology, Center for Excellence in Education (US), Tsinghua University (CN)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Beijing Municipal Science and Technology Commission, Beijing Municipal Natural Science Foundation
Openalex Percentile: Top 6%
SARS-CoV-2 and COVID-19 Research
4.19
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