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用于基因转移的纳米技术方法。

Nanotechnology approaches for gene transfer.

作者信息

Lundin Karin E, Simonson Oscar E, Moreno Pedro M D, Zaghloul Eman M, Oprea Iulian I, Svahn Mathias G, Smith C I Edvard

机构信息

Department of Laboratory Medicine, Clinical Research Center, Karolinska Institutet, Karolinska University Hospital, 141 86 Huddinge, Sweden.

出版信息

Genetica. 2009 Sep;137(1):47-56. doi: 10.1007/s10709-009-9372-0. Epub 2009 Jun 2.

Abstract

In both basic research as well as experimental gene therapy the need to transfer genetic material into a cell is of vital importance. The cellular compartment, which is the target for the genetic material, depends upon application. An siRNA that mediates silencing is preferably delivered to the cytosol while a transgene would need to end up in the nucleus for successful transcription to occur. Furthermore the ability to regulate gene expression has grown substantially since the discovery of RNA interference. In such diverse fields as medical research and agricultural pest control, the capability to alter the genetic output has been a useful tool for pushing the scientific frontiers. This review is focused on nanotechnological approaches to assemble optimised structures of nucleic acid derivatives to facilitate gene delivery as well as promoting down regulation of endogenous genes.

摘要

在基础研究以及实验性基因治疗中,将遗传物质导入细胞的需求至关重要。作为遗传物质靶标的细胞区室取决于应用情况。介导沉默的小干扰RNA(siRNA)最好递送至细胞质,而转基因则需要进入细胞核才能成功进行转录。此外,自RNA干扰被发现以来,调节基因表达的能力有了显著提高。在医学研究和农业害虫防治等诸多不同领域,改变基因输出的能力一直是推动科学前沿的有用工具。本综述聚焦于纳米技术方法,以组装核酸衍生物的优化结构,促进基因递送以及促进内源性基因的下调。

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