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

Author:

Figueroa Gerardo B.1ORCID,D'souza Simmone123ORCID,Pereira Higor S.1ORCID,Vasudeva Gunjan1ORCID,Figueroa Sara B.1ORCID,Robinson Zachary E.1ORCID,Badmalia Maulik D.14ORCID,Meier‐Stephenson Vanessa124ORCID,Corcoran Jennifer A.2ORCID,van Marle Guido2ORCID,Ni Yi56ORCID,Urban Stephan56ORCID,Coffin Carla S.23ORCID,Patel Trushar R.124ORCID

Affiliation:

1. Department of Chemistry and Biochemistry Alberta RNA Research and Training Institute, University of Lethbridge Lethbridge Alberta Canada

2. Department of Microbiology, Immunology and Infectious Diseases Cumming School of Medicine, University of Calgary Alberta Canada

3. Department of Medicine Cumming School of Medicine, University of Calgary Calgary Alberta Canada

4. Li Ka Shing Institute of Virology Faculty of Medicine & Dentistry, University of Alberta Edmonton Alberta Canada

5. Department of Infectious Diseases, Molecular Virology University Hospital Heidelberg Heidelberg Germany

6. German Center for Infection Research Heidelberg University Heidelberg Germany

Abstract

AbstractTo 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.

Funder

Canada Research Chairs

Alberta Innovates

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Diamond Light Source

Cumming School of Medicine, University of Calgary

Publisher

Wiley

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