HBcAg
乙型肝炎表面抗原
乙型肝炎病毒
化学
抗原
病毒学
病毒
体外
体内
生物
生物化学
免疫学
生物技术
作者
Xiao Guo,Maozhong Sun,Rui Gao,Aihua Qu,Chen Chen,Chuanlai Xu,Hua Kuang,Liguang Xu
标识
DOI:10.1002/anie.202103717
摘要
Abstract Hepatitis B virus (HBV) poses a severe threat to public health and social development. Here, we synthesized 4±0.5 nm copper (I) sulfide (Cu 2 S) nanoparticles (NPs) with 46 mdeg chiroptical property at 530 nm to selectively cleavage HBV core antigen (HBcAg) and effectively blocked HBV assembly and prevented HBV infection both in vitro and in vivo under light at 808 nm. Experimental analysis showed that the chiral Cu 2 S NPs specific bound with the functional domain from phenylalanine 23 (F 23 ) to leucine 30 (L 30 ) from HBcAg primary sequence and the cutting site was between amino acid residues F 24 and proline 25 (P 25 ). Under excitation at 808 nm, the intracellular HBcAg concentration was reduced by 95 %, and in HBV transgenic mice, the levels of HBV surface antigen (HBsAg) and HBV DNA were decreased by 93 % and 86 %, respectively. Together, these results reveal the potential nanomedicine for HBV control and provide fresh tools for viral infection.
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