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Updated: Jul 9, 2026

A Comparative Approach to Characterize the Landscape of Host-Pathogen Protein-Protein Interactions
Published on: July 18, 2013
AAV-2 Rep78 and HPV-16 E1 interact in vitro, modulating their ATPase activity
Sarmistha Bandyopadhyay1, Kevin D Raney, Yong Liu
1Department of Internal Medicine, Gene Therapy Program, University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, Arkansas 72205, USA.
Human papillomavirus (HPV) E1 protein interacts with adeno-associated virus (AAV) Rep78 protein. This interaction modulates their biochemical functions, offering insights into AAV DNA replication mechanisms.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Adeno-associated virus (AAV) requires helper viruses for efficient DNA replication.
- Human papillomavirus (HPV) can function as an AAV helper virus.
- The HPV-16 E1 protein is a key helper gene for AAV-2 DNA replication and transcription.
Purpose of the Study:
- To investigate the physical interaction between AAV Rep78 and HPV E1 proteins.
- To determine if the homology between Rep78 and E1 suggests a functional interaction.
- To explore the impact of this interaction on their respective biochemical activities.
Main Methods:
- Purification of full-length GST-E1 and MBP-Rep78 proteins from bacteria.
- Utilized five biochemical assays: pull-down, coimmunoprecipitation, ELISA, chemical cross-linking, and ATPase activity assays.
- Assessed the effect of combined protein presence on ATPase activity.
Main Results:
- Multiple assays provided consistent evidence of a physical interaction between Rep78 and E1.
- The ATPase activity of the proteins was decreased when both were present together.
- The interaction suggests modulation of individual protein functions.
Conclusions:
- AAV Rep78 and HPV E1 proteins physically interact.
- This interaction influences their biochemical functions, particularly ATPase activity.
- Provides foundational insights into the mechanism of HPV E1's helper function in AAV DNA replication.
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