Department of Chemistry and Biochemistry, Alberta RNA Research and Training Institute, University of Lethbridge, Lethbridge, Alberta, Canada.
Department of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine, University of Calgary, Alberta, Canada.
J Med Virol. 2024 Jun;96(6):e29692. doi: 10.1002/jmv.29692.
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.
为实现乙型肝炎病毒 (HBV) 的病毒学治愈,需要创新策略来靶向共价闭合环状 DNA (cccDNA) 基因组。鸟嘌呤四链体 (G4s) 是一种可以被 DNA 采用的二级结构,在调节病毒复制、转录和翻译方面发挥着重要作用。已经开发出基于抗体的探针和小分子来研究 G4s 在人类基因组中的作用,但没有专门针对病毒感染中 G4s 的。在此,我们描述了一种可以靶向 HBV cccDNA 基因组 PreCore (PreC) 启动子中 G4 的人源化单域抗体 (S10) 的开发。微量热泳动 (MicroScale Thermophoresis) 表明,S10 对 G4 形式的 PreC G4 具有很强的纳摩尔亲和力,并用小角度 X 射线散射确定了复合物的结构电子密度包络。S10 通过慢病毒转导进入 HepG2-NTCP 细胞显示核定位,染色质免疫沉淀结合下一代测序表明 S10 可以结合 cccDNA 上存在的 HBV PreC G4。这项研究验证了 HBV cccDNA 中存在 G4,并且表明可以使用 S10 针对这种 DNA 二级结构具有高结构和序列特异性。