Department of Bioscience and Biotechnology, Okayama University , 3-1-1 Tsushimanaka, Okayama, Japan.
Bioconjug Chem. 2011 Nov 16;22(11):2222-6. doi: 10.1021/bc200095a. Epub 2011 Oct 27.
RNA interference (RNAi) is being widely explored as a tool in functional genomics and tissue engineering, and in the therapy of intractable diseases, including cancer and neurodegenerative diseases. Recently, we developed a photoinducible RNAi method using photosensitizing carrier proteins, named CLIP-RNAi (CPP-linked RBP-mediated RNA internalization and photoinduced RNAi). Novel carrier proteins were designed for this study to establish a highly efficient delivery system for small interfering RNA (siRNA) or short hairpin RNA (shRNA) and to demonstrate light-dependent gene silencing. In addition, the results suggested that the dissociation of the siRNA (or shRNA) from carrier proteins in the cytoplasm is a critical event in CLIP-RNAi-mediated gene silencing.
RNA 干扰 (RNAi) 作为功能基因组学和组织工程学以及治疗难治性疾病(包括癌症和神经退行性疾病)的工具,正得到广泛的探索。最近,我们使用光敏载体蛋白开发了一种光诱导的 RNAi 方法,命名为 CLIP-RNAi(CPP 连接的 RBP 介导的 RNA 内化和光诱导的 RNAi)。为了建立高效的小干扰 RNA (siRNA) 或短发夹 RNA (shRNA) 传递系统,并证明光依赖性基因沉默,本研究设计了新型载体蛋白。此外,结果表明,siRNA(或 shRNA)从载体蛋白在细胞质中的解离是 CLIP-RNAi 介导的基因沉默的关键事件。