Evidence map›Paper›PMID 32290077›Full record

ArticleViruses2020

Molecular Mechanism of Evolution and Human Infection with SARS-CoV-2.

Jiahua He, Huanyu Tao, Yumeng Yan, Sheng-You Huang, Yi Xiao

Abstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing 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

83 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. RNA 3D Structure Prediction: Progress and Perspective.Molecules (Basel, Switzerland) · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Mutations in SARS-CoV-2: Insights on structure, variants, vaccines, and biomedical interventions.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

23 more citing papers are in PubMed but not listed here.

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

5 authors.

Jiahua HeInstitute of Biophysics, School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.
Huanyu TaoInstitute of Biophysics, School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.
Yumeng YanInstitute of Biophysics, School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.
Sheng-You HuangInstitute of Biophysics, School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.ORCID 0000-0002-4209-4565
Yi XiaoInstitute of Biophysics, School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.

Funding

National Natural Science Foundation of China 31670724
6 · The paper itself

Abstract

The outbreak of a novel coronavirus, which was later formally named the severe acute respiratory coronavirus 2 (SARS-CoV-2), has caused a worldwide public health crisis. Previous studies showed that SARS-CoV-2 is highly homologous to SARS-CoV and infects humans through the binding of the spike protein to ACE2. Here, we have systematically studied the molecular mechanisms of human infection with SARS-CoV-2 and SARS-CoV by protein-protein docking and MD simulations. It was found that SARS-CoV-2 binds ACE2 with a higher affinity than SARS-CoV, which may partly explain that SARS-CoV-2 is much more infectious than SARS-CoV. In addition, the spike protein of SARS-CoV-2 has a significantly lower free energy than that of SARS-CoV, suggesting that SARS-CoV-2 is more stable and may survive a higher temperature than SARS-CoV. This provides insights into the evolution of SARS-CoV-2 because SARS-like coronaviruses have originated in bats. Our computation also suggested that the RBD-ACE2 binding for SARS-CoV-2 is much more temperature-sensitive than that for SARS-CoV. Thus, it is expected that SARS-CoV-2 would decrease its infection ability much faster than SARS-CoV when the temperature rises. These findings would be beneficial for the disease prevention and drug/vaccine development of SARS-CoV-2.

Indexed as

Biological EvolutionAngiotensin-Converting Enzyme 2BetacoronavirusCoronavirus InfectionsCOVID-19Hot TemperatureHumansMolecular Docking SimulationMolecular Dynamics SimulationPandemicsPeptidyl-Dipeptidase APneumonia, ViralProtein BindingProtein StabilitySARS-CoV-2Severe acute respiratory syndrome-related coronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase ASpike Glycoprotein, Coronavirusspike glycoprotein, SARS-CoVcoronaviruseshuman infectionMD simulationsmolecular mechanismprotein dockingSARS-CoVSARS-CoV-2

Identifiers

PMID32290077
PMCPMC7232534

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.