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Development of a single-domain antibody to target a G-quadruplex located on the hepatitis B virus covalently closed circular DNA genome

To achieve a virological cure for hepatitis B virus (HBV), innovative strategies are required to target the covalently closed circular DNA (cccDNA) genome. Guanine-quadruplexes (G4s) are a secondary structure that can be adopted by DNA and play a significant role in regulating viral replication, tra...

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Main Authors: Figueroa, Gerardo B. (Author) , D'souza, Simmone (Author) , Pereira, Higor S. (Author) , Vasudeva, Gunjan (Author) , Figueroa, Sara B. (Author) , Robinson, Zachary E. (Author) , Badmalia, Maulik D. (Author) , Meier-Stephenson, Vanessa (Author) , Corcoran, Jennifer A. (Author) , van Marle, Guido (Author) , Ni, Yi (Author) , Urban, Stephan (Author) , Coffin, Carla S. (Author) , Patel, Trushar R. (Author)
Format: Article (Journal)
Language:English
Published: June 2024
In: Journal of medical virology
Year: 2024, Volume: 96, Issue: 6, Pages: 1-13
ISSN:1096-9071
DOI:10.1002/jmv.29692
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/jmv.29692
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/jmv.29692
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Author Notes:Gerardo B. Figueroa, Simmone D'souza, Higor S. Pereira, Gunjan Vasudeva, Sara B. Figueroa, Zachary E. Robinson, Maulik D. Badmalia, Vanessa Meier-Stephenson, Jennifer A. Corcoran, Guido van Marle, Yi Ni, Stephan Urban, Carla S. Coffin, Trushar R. Patel
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Summary:To achieve a virological cure for hepatitis B virus (HBV), innovative strategies are required to target the covalently closed circular DNA (cccDNA) genome. Guanine-quadruplexes (G4s) are a secondary structure that can be adopted by DNA and play a significant role in regulating viral replication, transcription, and translation. Antibody-based probes and small molecules have been developed to study the role of G4s in the context of the human genome, but none have been specifically made to target G4s in viral infection. Herein, we describe the development of a humanized single-domain antibody (S10) that can target a G4 located in the PreCore (PreC) promoter of the HBV cccDNA genome. MicroScale Thermophoresis demonstrated that S10 has a strong nanomolar affinity to the PreC G4 in its quadruplex form and a structural electron density envelope of the complex was determined using Small-Angle X-ray Scattering. Lentiviral transduction of S10 into HepG2-NTCP cells shows nuclear localization, and chromatin immunoprecipitation coupled with next-generation sequencing demonstrated that S10 can bind to the HBV PreC G4 present on the cccDNA. This research validates the existence of a G4 in HBV cccDNA and demonstrates that this DNA secondary structure can be targeted with high structural and sequence specificity using S10.
Item Description:Gesehen am 10.01.2025
Physical Description:Online Resource
ISSN:1096-9071
DOI:10.1002/jmv.29692

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