All Stories

  1. Host susceptibility and structural and immunological insight of S proteins of two SARS-CoV-2 closely related bat coronaviruses
  2. Optimization and Deoptimization of Codons in SARS‐CoV‐2 and Related Implications for Vaccine Development
  3. Adaptive Evolution of the Spike Protein in Coronaviruses
  4. A Competitive Panning Method Reveals an Anti-SARS-CoV-2 Nanobody Specific for an RBD-ACE2 Binding Site
  5. Effect of polymorphism in Rhinolophus affinis ACE2 on entry of SARS-CoV-2 related bat coronaviruses
  6. Mouse models susceptible to HCoV-229E and HCoV-NL63 and cross protection from challenge with SARS-CoV-2
  7. A Lentiviral Pseudotype System to Characterize SARS-CoV-2 Glycoprotein
  8. Characterization of SARS-CoV-2 Glycoprotein Using a Quantitative Cell–Cell Fusion System
  9. A Host-Harbored Metabolic Susceptibility of Coronavirus Enables Broad-Spectrum Targeting
  10. Relative vaccine effectiveness against Delta and Omicron COVID-19 after homologous inactivated vaccine boosting: a retrospective cohort study
  11. A comprehensive survey of bat sarbecoviruses across China in relation to the origins of SARS-CoV and SARS-CoV-2
  12. Optimization and deoptimization of codons in SARS-CoV-2 and the implications for vaccine development
  13. A Bispecific Antibody Targeting RBD and S2 Potently Neutralizes SARS-CoV-2 Omicron and Other Variants of Concern
  14. Simultaneous measurement of the antibody responses against SARS-CoV-2 and its multiple variants by a phage display mediated immuno-multiplex quantitative PCR-based assay
  15. A case–case study on the effect of primary and booster immunization with China-produced COVID-19 vaccines on prevention of pneumonia and viral load among vaccinated persons infected by Delta and Omicron variants
  16. Kathryn V. Holmes: A Career of Contributions to the Coronavirus Field
  17. A Bispecific Antibody Targeting RBD and S2 Potently Neutralizes SARS-CoV-2 Omicron and Other Variants of Concern
  18. The stalk domain of SARS-CoV-2 NSP13 is essential for its helicase activity
  19. Evolutionary dynamics of the severe acute respiratory syndrome coronavirus 2 genomes
  20. Negatively charged phospholipids accelerate the membrane fusion activity of the plant-specific insert domain of an aspartic protease
  21. SARS-CoV-2's origin should be investigated worldwide for pandemic prevention
  22. A comprehensive survey of bat sarbecoviruses across China for the origin tracing of SARS-CoV and SARS-CoV-2
  23. On the origin of SARS-CoV-2—The blind watchmaker argument
  24. The Rhinolophus affinis bat ACE2 and multiple animal orthologs are functional receptors for bat coronavirus RaTG13 and SARS-CoV-2
  25. Author Correction: Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV
  26. The Rhinolophus affinis bat ACE2 and multiple animal orthologs are functional receptors for bat coronavirus RaTG13 and SARS-CoV-2
  27. Insights into the mechanism of membrane fusion induced by the plant defense element, plant-specific insert
  28. Human monoclonal antibodies block the binding of SARS-CoV-2 spike protein to angiotensin converting enzyme 2 receptor
  29. Human monoclonal antibodies block the binding of SARS-CoV-2 spike protein to angiotensin converting enzyme 2 receptor
  30. Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV
  31. On the origin and continuing evolution of SARS-CoV-2
  32. Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study
  33. Glycine 29 Is Critical for Conformational Changes of the Spike Glycoprotein of Mouse Hepatitis Virus A59 Triggered by either Receptor Binding or High pH
  34. A highly efficient in vivo plasmid editing tool based on CRISPR-Cas12a and phage λ Red recombineering
  35. Identification of H209 as Essential for pH 8-Triggered Receptor-Independent Syncytium Formation by S Protein of Mouse Hepatitis Virus A59
  36. Crystal structure of the receptor binding domain of the spike glycoprotein of human betacoronavirus HKU1
  37. Structural and Molecular Evidence Suggesting Coronavirus-driven Evolution of Mouse Receptor
  38. Identification of the Fusion Peptide-Containing Region in Betacoronavirus Spike Glycoproteins
  39. Platform technology to generate broadly cross-reactive antibodies to α-helical epitopes in hemagglutinin proteins from influenza A viruses
  40. Deciphering the bat virome catalog to better understand the ecological diversity of bat viruses and the bat origin of emerging infectious diseases
  41. Identification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1
  42. Isolation, propagation, genome analysis and epidemiology of HKU1 betacoronaviruses
  43. Role of the Spike Glycoprotein of Human Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in Virus Entry and Syncytia Formation
  44. Human Coronavirus HKU1 Infection of Primary Human Type II Alveolar Epithelial Cells: Cytopathic Effects and Innate Immune Response
  45. Engineered Regulatory T Cells Coexpressing MHC Class II:Peptide Complexes Are Efficient Inhibitors of Autoimmune T Cell Function and Prevent the Development of Autoimmune Arthritis
  46. Innate Immune Response of Human Alveolar Type II Cells Infected with Severe Acute Respiratory Syndrome–Coronavirus
  47. Strategies for Designing Peptide Immunogens To Elicit α-Helical Conformation-Specific Antibodies Reactive with Native Proteins
  48. Crystal structure of mouse coronavirus receptor-binding domain complexed with its murine receptor
  49. An Autoantigen-Specific, Highly Restricted T Cell Repertoire Infiltrates the Arthritic Joints of Mice in an HLA-DR1 Humanized Mouse Model of Autoimmune Arthritis
  50. Complementation of a Binding-Defective Retrovirus by a Host Cell Receptor Mutant
  51. An Aromatic Side Chain Is Required at Residue 8 of SU for Fusion of Ecotropic Murine Leukemia Virus
  52. A Point Mutation in the Binding Subunit of a Retroviral Envelope Protein Arrests Virus Entry at Hemifusion
  53. Identification of a Critical Basic Residue on the Ecotropic Murine Leukemia Virus Receptor