Protein and Nucleic Acid Modifications in Response to Virus Infection

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Animal Viruses".

Deadline for manuscript submissions: closed (31 March 2022) | Viewed by 4771

Special Issue Editor


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Guest Editor
Associate Professor, Department of Microbiology and Immunology, University of Otago, Dunedin 9054, New Zealand
Interests: molecular virology; viral pathoegenesis; virus-host interactions; innate antiviral response; protein modifications; protein trafficking; acetylation
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Special Issue Information

Dear Colleagues,

Viruses utilise and exploit the host cell machinery to multiply. The inter- and intra-molecular interactions which play a critical role in virus–host interactions are known to be influenced by the complexity of the host proteome and transcriptome. Nevertheless, the layers of such complexity continue to unravel with the invention and application of new technologies. One of the phenomena which impacts this complexity is the reversible and irreversible modifications of both host and viral proteins as well as nucleic acids during infection. A plethora of such modifications, e.g., phosphorylation, glycosylation, acylation, methylation, and acetylation, etc., is known; many of them are dynamic and occur or change in response to virus infection. Many of these modifications have been known for some time, whereas many have been discovered recently. Nevertheless, the magnitude of these modifications in response to virus infection continues to unravel and is detrimental for comprehensive understanding of virus–host interactions. This Special Issue of Viruses invites articles reporting the latest research developments in this discipline of virology research.

Dr. Matloob Husain
Guest Editor

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Keywords

  • host and viral proteome
  • omics
  • protein modifications
  • DNA and RNA modifications
  • acetylation
  • methylation

Published Papers (1 paper)

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Research

22 pages, 47268 KiB  
Article
Acetylation, Methylation and Allysine Modification Profile of Viral and Host Proteins during Influenza A Virus Infection
by Farjana Ahmed, Torsten Kleffmann and Matloob Husain
Viruses 2021, 13(7), 1415; https://doi.org/10.3390/v13071415 - 20 Jul 2021
Cited by 12 | Viewed by 4054
Abstract
Protein modifications dynamically occur and regulate biological processes in all organisms. Towards understanding the significance of protein modifications in influenza virus infection, we performed a global mass spectrometry screen followed by bioinformatics analyses of acetylation, methylation and allysine modification in human lung epithelial [...] Read more.
Protein modifications dynamically occur and regulate biological processes in all organisms. Towards understanding the significance of protein modifications in influenza virus infection, we performed a global mass spectrometry screen followed by bioinformatics analyses of acetylation, methylation and allysine modification in human lung epithelial cells in response to influenza A virus infection. We discovered 8 out of 10 major viral proteins and 245 out of 2280 host proteins detected to be differentially modified by three modifications in infected cells. Some of the identified proteins were modified on multiple amino acids residues and by more than one modification; the latter occurred either on different or same residues. Most of the modified residues in viral proteins were conserved across >40 subtypes of influenza A virus, and influenza B or C viruses and located on the protein surface. Importantly, many of those residues have already been determined to be critical for the influenza A virus. Similarly, many modified residues in host proteins were conserved across influenza A virus hosts like humans, birds, and pigs. Finally, host proteins undergoing the three modifications clustered in common functional networks of metabolic, cytoskeletal, and RNA processes, all of which are known to be exploited by the influenza A virus. Full article
(This article belongs to the Special Issue Protein and Nucleic Acid Modifications in Response to Virus Infection)
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