寡核苷酸
计算生物学
生物结合
核糖核酸酶H
核糖核酸
RNA剪接
核糖核酸酶P
RNA干扰
基因
化学
生物
遗传学
生物化学
作者
Thomas C. Roberts,Róbert Langer,Matthew J. A. Wood
标识
DOI:10.1038/s41573-020-0075-7
摘要
Oligonucleotides can be used to modulate gene expression via a range of processes including RNAi, target degradation by RNase H-mediated cleavage, splicing modulation, non-coding RNA inhibition, gene activation and programmed gene editing. As such, these molecules have potential therapeutic applications for myriad indications, with several oligonucleotide drugs recently gaining approval. However, despite recent technological advances, achieving efficient oligonucleotide delivery, particularly to extrahepatic tissues, remains a major translational limitation. Here, we provide an overview of oligonucleotide-based drug platforms, focusing on key approaches - including chemical modification, bioconjugation and the use of nanocarriers - which aim to address the delivery challenge.
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