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Coat Assembly and GTPases01:33

Coat Assembly and GTPases

Vesicles incorporate different coat protein subunits in different cell locations, which changes the properties of the coat, such as the shape and geometry of the transport vesicles. Thus, vesicle coat proteins also play a significant role in cargo selection.
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Viruses are unique biological entities that blur the boundary between living and non-living systems. Although they lack cellular structure and metabolic processes, they can exhibit characteristics of life when infecting a host. Their defining feature is a nucleic acid core, composed of either DNA or RNA, encapsulated within a protein coat called a capsid. This simple structure allows them to invade host cells and use their machinery for replication efficiently.Viral Structure and...
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Updated: May 20, 2026

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting
08:40

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting

Published on: March 1, 2019

Poxvirus cell entry: how many proteins does it take?

Bernard Moss1

  • 1Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. bmoss@nih.gov

Viruses
|July 4, 2012
PubMed
Summary
This summary is machine-generated.

Poxviruses utilize an unprecedented number of proteins for cell entry, unlike other viruses. Fusion requires a complex of 11-12 transmembrane proteins, suggesting a conserved viral entry mechanism.

Keywords:
endocytosismacropinocytosistransmembrane proteinsvaccinia virus entryviral membrane fusion

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Area of Science:

  • Virology
  • Cellular Biology
  • Molecular Biology

Background:

  • Many viruses use 1-2 proteins for cell entry, but poxviruses employ numerous proteins, potentially enabling broad cell tropism.
  • Poxviruses exist as mature virions (MV) and extracellular enveloped virions (EV), with distinct membrane structures and attachment mechanisms.
  • MV attachment involves four viral proteins binding to cell surface molecules like glycosaminoglycans.

Purpose of the Study:

  • To investigate the protein requirements and mechanisms of poxvirus entry into host cells.
  • To elucidate the conserved viral entry pathways across different poxvirus forms (MV and EV).

Main Methods:

  • Analysis of viral protein composition and function during cell entry.
  • Biochemical studies to understand membrane fusion processes.
  • Comparative analysis of MV and EV entry pathways.

Main Results:

  • Poxvirus entry involves a complex of 11-12 non-glycosylated transmembrane proteins, conserved across poxviruses.
  • Viral entry can occur at the plasma membrane or via endosomes, involving actin dynamics and cell signaling.
  • Membrane fusion proceeds in a two-step manner: lipid mixing followed by pore expansion and core penetration.

Conclusions:

  • The extensive protein machinery in poxviruses is linked to their ability to infect diverse cell types.
  • A conserved mechanism involving a multi-protein complex mediates poxvirus fusion, regardless of the entry pathway or virion form.
  • Understanding poxvirus entry provides insights into viral pathogenesis and potential therapeutic targets.