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Related Concept Videos

Viral Structure00:56

Viral Structure

Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
Inhibitors Of Virion Release01:25

Inhibitors Of Virion Release

Viral replication and dissemination rely on efficient mechanisms for host cell entry, genome replication, assembly, and release. Influenza viruses, such as types A and B, are negative-sense single-stranded RNA viruses with a segmented genome, that depend on two critical surface glycoproteins to carry out these processes: hemagglutinin (HA) and neuraminidase (NA). HA initiates infection by binding to sialic acid residues on the surface of host epithelial cells, facilitating receptor-mediated...
Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
Subviral Agents01:29

Subviral Agents

Subviral agents are infectious entities that resemble viruses but lack one or more viral components, such as a capsid or essential replication machinery. These agents include viroids, prions, and satellites, each possessing distinct structural and functional characteristics that influence their mode of infection and replication.Viroids are the simplest subviral agents, consisting of circular, single-stranded RNA molecules without a protein coat. They exclusively infect plants, relying entirely...
Inhibitors of Virion Maturation and Assembly01:19

Inhibitors of Virion Maturation and Assembly

As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...

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Related Experiment Video

Updated: Jun 28, 2026

Quantifying Human Norovirus Virus-like Particles Binding to Commensal Bacteria Using Flow Cytometry
07:02

Quantifying Human Norovirus Virus-like Particles Binding to Commensal Bacteria Using Flow Cytometry

Published on: April 29, 2020

Noroviral P particle: structure, function and applications in virus-host interaction.

Ming Tan1, Pingan Fang, Teepanis Chachiyo

  • 1Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.

Virology
|October 18, 2008
PubMed
Summary

Noroviruses cause epidemic gastroenteritis by binding to human histo-blood group antigens (HBGAs). Subviral P particles retain this binding function and show potential for norovirus vaccine development.

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Last Updated: Jun 28, 2026

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Quantifying Human Norovirus Virus-like Particles Binding to Commensal Bacteria Using Flow Cytometry

Published on: April 29, 2020

Production of Human Norovirus Protruding Domains in E. coli for X-ray Crystallography
10:46

Production of Human Norovirus Protruding Domains in E. coli for X-ray Crystallography

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Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses
08:10

Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses

Published on: January 15, 2020

Area of Science:

  • Virology
  • Structural Biology
  • Immunology

Background:

  • Noroviruses are a major cause of epidemic acute gastroenteritis.
  • These viruses utilize human histo-blood group antigens (HBGAs) as cellular receptors.
  • The protruding (P) domain of the norovirus capsid contains the receptor-binding site and can form subviral particles (P particles) in vitro.

Purpose of the Study:

  • To characterize the structure and HBGA-binding function of norovirus P particles.
  • To evaluate the potential of P particles for vaccine development.

Main Methods:

  • Cryo-electron microscopy (cryo-EM) for structural reconstruction.
  • Biochemical assays to assess HBGA-binding.
  • Immunogenicity studies.
  • Production of P particles in E. coli and yeast.

Main Results:

  • P particles are composed of 12 P dimers arranged in octahedral symmetry.
  • The dimeric packing resembles that of the norovirus capsid, with the receptor-binding interface exposed.
  • P particles are immunogenic and share antigenic and HBGA-binding profiles with virus-like particles.
  • P particles are stable and readily produced in microbial systems.

Conclusions:

  • Norovirus P particles possess a defined structure mimicking the viral capsid's surface.
  • P particles effectively bind to HBGAs and are immunogenic.
  • Their stability and ease of production suggest significant potential for norovirus vaccine development.