Bubbled RNA‐Based Cargo for Boosting RNA Interference
Source abstract
Abstract
As ribonucleic acid (RNA) nanotechnology has advanced, it has been applied widely in RNA‐based therapeutics. Among the range of approaches, enzymatically synthesized RNA structures for inducing RNA interference in cancer cells have potential for silencing genes in a target‐specific manner. On the other hand, the efficiency of gene silencing needs to be improved to utilize the RNA‐based system for RNAi therapeutics. This paper introduces a new approach for efficient generation of siRNA from bubbled RNA‐based cargo (BRC). The presence of bubbles in between to avoid nonfunctional short dsRNAs allows the RNA‐based cargoes to contain multiple Dicer‐cleavage sites to release the functional siRNAs when introduced to cells. BRCs can be synthesized easily in a one‐pot process and be purified by simple centrifugation. Furthermore, efficient target gene silencing by the bubbled structure is confirmed both in vitro and in vivo. Therefore, this bubbled RNA cargo system can be utilized for target‐specific RNAi therapeutics with high efficiency in the generation of functional siRNAs in the target cells.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: RNA Interference and Gene Delivery · Advanced biosensing and bioanalysis techniques · Bacteriophages and microbial interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering University of Seoul 163 Seoulsiripdaero Dongdaemun‐gu Seoul 02504 Republic of Korea
KU‐KIST Graduate School of Converging Science and Technology Korea University 145 Anam‐ro Seongbuk‐gu, Seoul 02841 Republic of Korea
Center for Theragnosis Biomedical Research Institute Korea Institute of Science and Technology (KIST) Seoul 02792 Republic of Korea
Funding
National Research Foundation of Korea
References (24)
Show source-provided references
1. 10.1038/nrd362510.1038/nrd3625 ↗
2. 10.1073/pnas.160029911310.1073/pnas.1600299113 ↗
3. 10.1038/nnano.2010.23110.1038/nnano.2010.231 ↗
4. 10.1021/ar500076k10.1021/ar500076k ↗
5. 10.1016/0022-5193(82)90002-910.1016/0022-5193(82)90002-9 ↗
6. 10.1021/bi00237a00510.1021/bi00237a005 ↗
7. 10.1038/382607a010.1038/382607a0 ↗
8. 10.1089/nat.2012.035010.1089/nat.2012.0350 ↗
9. 10.1021/acscombsci.5b0010810.1021/acscombsci.5b00108 ↗
10. 10.1038/nprot.2011.41810.1038/nprot.2011.418 ↗
11. Halman J. R. · Nucleic Acids Res. · 2017 · 45 · 2210
12. 10.1021/nn502253c10.1021/nn502253c ↗
13. 10.1016/j.addr.2015.10.00810.1016/j.addr.2015.10.008 ↗
14. 10.1038/nbt0397-27310.1038/nbt0397-273 ↗
15. 10.1021/ja00134a03210.1021/ja00134a032 ↗
16. 10.1038/nmat325310.1038/nmat3253 ↗
17. 10.1038/srep1273710.1038/srep12737 ↗
18. 10.1038/ncomms536710.1038/ncomms5367 ↗
19. 10.1038/srep2514610.1038/srep25146 ↗
20. 10.1021/acsbiomaterials.5b0055410.1021/acsbiomaterials.5b00554 ↗
21. 10.1038/nnano.2012.21110.1038/nnano.2012.211 ↗
22. 10.1039/C4CC04969A10.1039/C4CC04969A ↗
23. 10.1002/smll.20130267610.1002/smll.201302676 ↗
24. 10.1126/science.112163810.1126/science.1121638 ↗