The joys of in vitro selection: chemically dressing oligonucleotides to satiate protein targets

被引:86
作者
Eaton, BE [1 ]
机构
[1] NeXstar Pharmaceut Inc, Boulder, CO 80301 USA
关键词
D O I
10.1016/S1367-5931(97)80103-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oligonucleotide in vitro selection provides surprisingly specific aptamers to protein targets. Synthetic chemistries for modifying nucleotides have been developed to enhance aptamer binding affinity. The diversity of nucleosides amenable to either triphosphate synthesis or phosphoramidite activation is now sufficiently broad to rival any oligomeric combinatorial library.
引用
收藏
页码:10 / 16
页数:7
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