Shu Yi, Shu Dan, Diao Zhijuan, Shen Guanxin, Guo Peixuan
Department of Biomedical Engineering, College of Medicine/College of Engineering, University of Cincinnati, 3125 Eden Ave., Cincinnati, OH, USA.
IEEE NIH Life Sci Syst Appl Workshop. 2009 May 2;2009:9-12. doi: 10.1109/LISSA.2009.4906696.
Bacteriophage phi29 DNA packaging motor is geared by a six-pRNA ring. pRNA is able to form a multimeric complex and patterned superstructures via the interaction of two reengineered interlocking loops. This unique feature makes it an ideal polyvalent vehicle for nanomachine fabrication, pathogen detection, and the delivery of therapeutics. This report describes novel approaches for the fabrication of polyvalent therapeutic pRNA nanoparticles, especially tetramers for specific siRNA delivery to cancer cells and for the silencing of targeted genes. RNA 3-D design, circular permutation, folding energy alteration, and nucleotide modification were applied to generate stable RNA nanoparticles with low toxicity. Animal trials demonstrated the high efficiency of the polyvalent RNA nanoparticles in the prevention and treatment of cancer. Using such protein-free nanoparticles as therapeutic reagents would allow for long-term administration to avoid the induction of antibody due to repeated treatment for chronic diseases.
噬菌体phi29 DNA包装马达由一个六聚体pRNA环驱动。pRNA能够通过两个重新设计的互锁环的相互作用形成多聚体复合物和有图案的超结构。这一独特特性使其成为纳米机器制造、病原体检测和治疗药物递送的理想多价载体。本报告描述了制造多价治疗性pRNA纳米颗粒的新方法,特别是用于将特定siRNA递送至癌细胞并沉默靶向基因的四聚体。应用RNA三维设计、环形排列、折叠能量改变和核苷酸修饰来生成低毒性的稳定RNA纳米颗粒。动物试验证明了多价RNA纳米颗粒在癌症预防和治疗中的高效性。使用这种无蛋白质的纳米颗粒作为治疗试剂将允许长期给药,以避免因慢性疾病的重复治疗而诱导抗体。