posted on 2024-12-27, 02:44authored byMeng-Fan Feng, Li-Miao Qin, Bo Sun, Xianghui Yu, Yuqing Wu
Circular RNA (circRNA) has emerged
as a promising class of therapeutics
and mRNA vaccines. While possessing greater stability and functionality
akin to linear mRNA, circRNA still necessitates an efficient and adaptable
delivery system to surmount the primary challenge of cellular uptake
and membrane penetration. Inspired by the high invasiveness of the
virus, in this study, the virus-like nanoparticles (VLNPs) of human
papillomavirus (HPV) have been constructed as robust carriers for
circRNA encapsulation and transfer through their coassembly monitoring.
Notably, the functionalization of a transmembrane peptide (L17E) on
the outer surface of VLNPs has led to the development of a more efficient
nanocarrier, which has significantly enhanced both the transmembrane
delivery and endosomal escape of circRNA. Validation studies employing
VLNPs-L17E-packaged circRNA across various cell types have demonstrated
notable improvements in target protein expression, ranging from 1.48-
to 2.04-fold. These findings underscore the potential of HPV-VLNPs-L17E
as a carrier for circRNA delivery, offering promising prospects for
RNA therapy applications in the future.