Glycomics and Proteomics Approaches to Investigate Early Adenovirus–Host Cell Interactions. Issue 13 (22nd June 2018)
- Record Type:
- Journal Article
- Title:
- Glycomics and Proteomics Approaches to Investigate Early Adenovirus–Host Cell Interactions. Issue 13 (22nd June 2018)
- Main Title:
- Glycomics and Proteomics Approaches to Investigate Early Adenovirus–Host Cell Interactions
- Authors:
- Lasswitz, Lisa
Chandra, Naresh
Arnberg, Niklas
Gerold, Gisa - Abstract:
- Abstract: Adenoviruses as most viruses rely on glycan and protein interactions to attach to and enter susceptible host cells. The Adenoviridae family comprises more than 80 human types and they differ in their attachment factor and receptor usage, which likely contributes to the diverse tropism of the different types. In the past years, methods to systematically identify glycan and protein interactions have advanced. In particular sensitivity, speed and coverage of mass spectrometric analyses allow for high-throughput identification of glycans and peptides separated by liquid chromatography. Also, developments in glycan microarray technologies have led to targeted, high-throughput screening and identification of glycan-based receptors. The mapping of cell surface interactions of the diverse adenovirus types has implications for cell, tissue, and species tropism as well as drug development. Here we review known adenovirus interactions with glycan- and protein-based receptors, as well as glycomics and proteomics strategies to identify yet elusive virus receptors and attachment factors. We finally discuss challenges, bottlenecks, and future research directions in the field of non-enveloped virus entry into host cells. Graphical abstract: Unlabelled Image Highlights: Adenovirus entry into cells is guided by specific glycan and protein interactions. Glycan arrays and shotgun glycomics methods are valuable technologies to identify virus–glycan interactions. Shotgun proteomics andAbstract: Adenoviruses as most viruses rely on glycan and protein interactions to attach to and enter susceptible host cells. The Adenoviridae family comprises more than 80 human types and they differ in their attachment factor and receptor usage, which likely contributes to the diverse tropism of the different types. In the past years, methods to systematically identify glycan and protein interactions have advanced. In particular sensitivity, speed and coverage of mass spectrometric analyses allow for high-throughput identification of glycans and peptides separated by liquid chromatography. Also, developments in glycan microarray technologies have led to targeted, high-throughput screening and identification of glycan-based receptors. The mapping of cell surface interactions of the diverse adenovirus types has implications for cell, tissue, and species tropism as well as drug development. Here we review known adenovirus interactions with glycan- and protein-based receptors, as well as glycomics and proteomics strategies to identify yet elusive virus receptors and attachment factors. We finally discuss challenges, bottlenecks, and future research directions in the field of non-enveloped virus entry into host cells. Graphical abstract: Unlabelled Image Highlights: Adenovirus entry into cells is guided by specific glycan and protein interactions. Glycan arrays and shotgun glycomics methods are valuable technologies to identify virus–glycan interactions. Shotgun proteomics and ligand-based receptor capture are powerful methods for proteinaceous receptor discovery. A combination of shotgun glycomics and proteomics with CRISPR/Cas9 and RNAi validation holds the promise of generating a systems biology view of virus entry processes. … (more)
- Is Part Of:
- Journal of molecular biology. Volume 430:Issue 13(2018)
- Journal:
- Journal of molecular biology
- Issue:
- Volume 430:Issue 13(2018)
- Issue Display:
- Volume 430, Issue 13 (2018)
- Year:
- 2018
- Volume:
- 430
- Issue:
- 13
- Issue Sort Value:
- 2018-0430-0013-0000
- Page Start:
- 1863
- Page End:
- 1882
- Publication Date:
- 2018-06-22
- Subjects:
- adenovirus -- virus entry -- proteomics -- glycomis -- host cell interactions
HAdVs human adenoviruses -- LSFs long-shafted fibers -- SSFs short-shafted fibers -- SA Sialic acid -- IAVs influenza A viruses -- GAGs glycosaminoglycans -- HS heparan sulfate -- HSPG heparan sulfate proteoglycan -- HBGAs histo blood group antigens -- GSLs glycosphingolipids -- CAR coxsackie and adenovirus receptor -- VCAM-1 vascular cell adhesion molecule-1 -- MHC-I major histocompatibility complex 1 -- CFG Consortium for Functional Glycomics -- SG shotgun glycomics -- ICL Imperial College of London -- VOPBAs virus overlay protein binding assays -- VAPs virus attachment proteins -- AE-MS affinity enrichment mass spectrometry
Molecular biology -- Periodicals
Biology -- Periodicals
Biochemistry -- Periodicals
Bacteriology -- Periodicals
Molecular Biology -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biologie -- Périodiques
Biochimie -- Périodiques
Moleculaire biologie
Biochemistry
Biology
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222836 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jmb.2018.04.039 ↗
- Languages:
- English
- ISSNs:
- 0022-2836
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.700000
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