Evidence map›Paper›PMID 40944451›Full record

ArticleProtein science : a publication of the Protein Society2025

Rational design of a covalent ACE2 decoy receptor that broadly neutralizes SARS-CoV-2 variants.

Nobumasa Hino, Risa Takada, Kyosuke Suzuki, Nagisa Tokunoh, Tatsuya Karaki, Kazumasa Ohtake, Haruna Ogami, Takafumi Nishiura, Kenji Ishimoto, Tomohito Tsukamoto and 9 more

Abstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Nobumasa HinoLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.ORCID 0000-0002-7072-1183
Risa TakadaLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Kyosuke SuzukiLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Nagisa TokunohVaccine Creation Group, BIKEN Innovative Vaccine Research Alliance Laboratories, Research Institute for Microbial Diseases, The University of Osaka, Osaka, Japan.
Tatsuya KarakiVaccine Creation Group, BIKEN Innovative Vaccine Research Alliance Laboratories, Research Institute for Microbial Diseases, The University of Osaka, Osaka, Japan.
Kazumasa OhtakeLaboratory for Nonnatural Amino Acid Technology, RIKEN Center for Biosystems Dynamics Research, Kanagawa, Japan.
Haruna OgamiLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Takafumi NishiuraLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Kenji IshimotoLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Tomohito TsukamotoLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Yukio AgoLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Yoshiaki OkadaLaboratory of Clinical Science and Biomedicine, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Toru OkamotoInstitute for Advanced Co-Creation Studies, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Chikako OnoCenter for Infectious Disease Education and Research, The University of Osaka, Osaka, Japan.
Yoshiharu MatsuuraCenter for Infectious Disease Education and Research, The University of Osaka, Osaka, Japan.
Satoshi ObikaLaboratory of Bioorganic Chemistry, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.
Kensaku SakamotoLaboratory for Nonnatural Amino Acid Technology, RIKEN Center for Biosystems Dynamics Research, Kanagawa, Japan.
Yasuo YoshiokaCenter for Infectious Disease Education and Research, The University of Osaka, Osaka, Japan.
Shinsaku NakagawaLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, Osaka, Japan.

Funding

Japan Agency for Medical Research and Development JP25ama121052Japan Agency for Medical Research and Development JP25ama121054Japan Society for the Promotion of Science 23K18004Japan Society for the Promotion of Science 25K01950RIKEN-Osaka University Science & Technology Hub Collaborative Research ProgramThe Nippon Foundation
6 · The paper itself

Abstract

The ongoing evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the emergence of variants that evade existing vaccines and antibody therapies necessitate novel, potent, and broad-spectrum antiviral strategies. Enhancing therapeutic proteins with additional covalent binding capabilities, such as minibinders and nanobodies, reportedly potentiates their antiviral efficacy by irreversibly capturing the viral cell-entry protein. However, viral mutations that interfere with covalent bonding or reduce viral affinity with therapeutic proteins might compromise the efficacy of this strategy. Therefore, in this study, we aimed to develop a broadly neutralizing covalent angiotensin-converting enzyme 2-Fc (ACE2-Fc) decoy using a rational design strategy that integrates functional genomics with structural information. Using this approach, we targeted a highly conserved and functionally constrained residue on the viral receptor-binding domain (RBD) and identified tyrosine 473 (Y473) as an optimal target. We engineered ACE2-Fc constructs by replacing glutamate 23 (E23) and threonine 27 (T27) with the non-canonical amino acid-fluorosulfate-L-tyrosine (FSY), generating E23FSY and T27FSY constructs. These constructs formed a specific and efficient covalent bond with Y473 of the RBD. Notably, this covalent capture was retained against the highly mutated Omicron BA.5 RBD. In pseudovirus neutralization assays, both E23FSY and T27FSY exhibited markedly enhanced potency against both wild-type-like (D614G) and Omicron variants compared to their non-covalent counterparts. These results demonstrate that using an inherently escape-resistant decoy receptor to covalently target evolutionarily constrained residues on the viral RBD is a highly efficient strategy for creating potent, broad-spectrum covalent inhibitors against rapidly evolving viruses such as SARS-CoV-2.

Indexed as

Angiotensin-Converting Enzyme 2SARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingCOVID-19HumansACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ACE2‐Fccovalent proteinscross‐linkinggenetic code expansionnon‐canonical amino acidsSARS‐CoV‐2

Identifiers

PMID40944451
PMCPMC12432405

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.