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针对mRNA序列特异性敲低的方法。

Approaches for the sequence-specific knockdown of mRNA.

作者信息

Scherer Lisa J, Rossi John J

机构信息

Division of Molecular Biology, Beckman Research Institute of the City of Hope, Duarte, California 91010, USA.

出版信息

Nat Biotechnol. 2003 Dec;21(12):1457-65. doi: 10.1038/nbt915.

Abstract

Over the past 25 years there have been thousands of published reports describing applications of antisense nucleic acid derivatives for targeted inhibition of gene function. The major classes of antisense agents currently used by investigators for sequence-specific mRNA knockdowns are antisense oligonucleotides (ODNs), ribozymes, DNAzymes and RNA interference (RNAi). Whatever the method, the problems for effective application are remarkably similar: efficient delivery, enhanced stability, minimization of off-target effects and identification of sensitive sites in the target RNAs. These challenges have been in existence from the first attempts to use antisense research tools, and need to be met before any antisense molecule can become widely accepted as a therapeutic agent.

摘要

在过去25年里,已有数千篇发表的报告描述了反义核酸衍生物在靶向抑制基因功能方面的应用。研究人员目前用于序列特异性敲低mRNA的主要反义剂类别包括反义寡核苷酸(ODN)、核酶、脱氧核酶和RNA干扰(RNAi)。无论采用何种方法,有效应用的问题都非常相似:高效递送、增强稳定性、将脱靶效应降至最低以及识别靶RNA中的敏感位点。从首次尝试使用反义研究工具开始,这些挑战就一直存在,并且在任何反义分子能够被广泛接受为治疗剂之前都需要加以应对。

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