Related Experiment Video
Updated: Nov 28, 2025

Isolation of Viral Replication Compartment-enriched Sub-nuclear Fractions from Adenovirus-infected Normal Human Cells
Published on: November 12, 2015
Structural Organization and Protein-Protein Interactions in Human Adenovirus Capsid
Vijay S Reddy1, Michael A Barry2
1Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA, 92037, USA. reddyv@scripps.edu.
Abstract:
Human adenoviruses (HAdVs) are large (150 MDa), complex, nonenveloped dsDNA viruses that cause self-limiting respiratory, ocular and enteric infections. They are significant health hazard in young, elderly and immuno-compromised populations. Moreover, various adenoviruses (AdVs) of mammalian origin are being used as vectors in gene, vaccine and cancer therapies. Multiple copies of at least 13 different proteins, all in all ~2800 protein molecules, come together to form an adenovirus virion packaging the ~36 Kbp geome. The details of structural organization of the adenovirus capsid and underlying network of protein-protein interactions provide clues into designing the modified and novel adenovirus vectors with desired functionalities and/or targeting specificities. The advancements in 3D structure determination by cryo-electron microscopy (cryo-EM) in the past decade have enabled unveiling of the complex organization of adenovirus architecture at near atomic resolution. Specifically, these studies revealed the structures and the network of interactions involving cement/minor proteins in stabilizing the AdV icosahedral architecture, which appear to be mostly conserved among human adenoviruses. In this chapter, we describe the current state of knowledge on the structure and organization of human adenoviruses.
Insights
Human adenoviruses (HAdVs) are complex viruses causing infections and used in therapies. Advanced cryo-electron microscopy reveals their structural organization and protein interactions for improved vector design.
Area of Science:
- Virology
- Structural Biology
- Biochemistry
Background:
- Human adenoviruses (HAdVs) are nonenveloped dsDNA viruses responsible for various infections.
- HAdVs pose health risks, particularly to vulnerable populations.
- Adenoviruses are crucial as vectors in gene, vaccine, and cancer therapies.
Purpose of the Study:
- To detail the current understanding of human adenovirus structure and organization.
- To explore the protein-protein interactions within the adenovirus capsid.
- To highlight how structural insights inform the design of novel adenovirus vectors.
Main Methods:
- Utilizing advancements in cryo-electron microscopy (cryo-EM) for 3D structure determination.
- Analyzing near-atomic resolution structures of adenovirus architecture.
- Investigating the role of specific proteins, like cement/minor proteins, in capsid stabilization.
Main Results:
- Cryo-EM has unveiled the intricate organization of adenovirus architecture.
- Identified the network of protein-protein interactions stabilizing the viral capsid.
- Observed conserved structural features and protein interactions among human adenoviruses.
Conclusions:
- The detailed structure of human adenoviruses is increasingly understood through cryo-EM.
- Understanding capsid protein interactions is key to adenovirus vector development.
- Structural insights facilitate the design of modified adenoviruses with enhanced functionalities.
More Related Videos
08:14Combined Genetic and Chemical Capsid Modifications of Adenovirus-Based Gene Transfer Vectors for Shielding and Targeting
Published on: October 26, 2018
13:36Utilizing the Antigen Capsid-Incorporation Strategy for the Development of Adenovirus Serotype 5-Vectored Vaccine Approaches
Published on: May 6, 2015
Related Concept Videos
Viral Structure
Protein Complex Assembly
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Introduction to Virus
Protein Organization
The primary structure of a protein is its amino acid sequence....
Protein Organization
Size and Structure of Viral Genomes