Glycomics and Proteomics Approaches to Investigate Early Adenovirus-Host Cell Interactions

Lisa Lasswitz1, Naresh Chandra2, Niklas Arnberg2

  • 1Institute for Experimental Virology, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Medical School Hannover and the Helmholtz Centre for Infection Research, 30625 Hannover, Germany.

Insights

Adenoviruses use glycan and protein interactions for cell entry. Advanced glycomics and proteomics methods help identify these crucial viral receptors and attachment factors, impacting tropism and drug development.

Area of Science:

  • Virology
  • Glycobiology
  • Proteomics

Background:

  • Adenoviruses, a large family of viruses, utilize specific glycan and protein interactions to infect host cells.
  • Diverse human adenovirus types exhibit varied tropism due to differences in attachment factors and receptor usage.
  • Understanding these interactions is key to deciphering viral entry mechanisms.

Purpose of the Study:

  • To review known adenovirus interactions with glycan and protein receptors.
  • To explore glycomics and proteomics strategies for identifying novel virus receptors and attachment factors.
  • To discuss implications for viral tropism and antiviral drug development.

Main Methods:

  • Review of existing literature on adenovirus-receptor interactions.
  • Discussion of advancements in mass spectrometry for glycan and peptide identification.
  • Highlighting developments in glycan microarray technologies for high-throughput screening.

Main Results:

  • Adenovirus attachment and entry are mediated by specific glycan and protein interactions.
  • High-throughput analytical techniques enable systematic identification of these interactions.
  • Mapping these interactions provides insights into viral tropism and host range.

Conclusions:

  • Advanced glycomics and proteomics are essential for identifying elusive adenovirus receptors.
  • Understanding virus-host interactions is critical for developing targeted antiviral therapies.
  • Future research should focus on overcoming challenges in studying non-enveloped virus entry.

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