Aptamers as therapeutics

被引:1680
作者
Keefe, Anthony D. [1 ]
Pai, Supriya [1 ]
Ellington, Andrew [1 ]
机构
[1] Univ Texas Austin, Inst Cell & Mol Biol, Austin, TX 78712 USA
关键词
AFFINITY RNA LIGANDS; IN-VITRO SELECTION; IMMUNODEFICIENCY-VIRUS TYPE-1; TARGETED DRUG-DELIVERY; PROSTATE-CANCER CELLS; COMBINATORIAL SELECTION; VASCULAR-PERMEABILITY; SYSTEMATIC EVOLUTION; AUTOMATED SELECTION; SIRNA DELIVERY;
D O I
10.1038/nrd3141
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nucleic acid aptamers can be selected from pools of random-sequence oligonucleotides to bind a wide range of biomedically relevant proteins with affinities and specificities that are comparable to antibodies. Aptamers exhibit significant advantages relative to protein therapeutics in terms of size, synthetic accessibility and modification by medicinal chemistry. Despite these properties, aptamers have been slow to reach the marketplace, with only one aptamer-based drug receiving approval so far. A series of aptamers currently in development may change how nucleic acid therapeutics are perceived. It is likely that in the future, aptamers will increasingly find use in concert with other therapeutic molecules and modalities.
引用
收藏
页码:537 / 550
页数:14
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