Bioactive and nuclease-resistant L-DNA ligand of vasopressin

被引:179
作者
Williams, KP
Liu, XH
Schumacher, TNM
Lin, HY
Ausiello, DA
Kim, PS
Bartel, DP
机构
[1] MIT,WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142
[2] MIT,DEPT BIOL,CAMBRIDGE,MA 02142
[3] HOWARD HUGHES MED INST,CAMBRIDGE CTR 9,CAMBRIDGE,MA 02142
[4] MASSACHUSETTS GEN HOSP,DEPT MED,PROGRAM MEMBRANE BIOL,RENAL UNIT,CHARLESTOWN,MA 02129
关键词
D O I
10.1073/pnas.94.21.11285
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In vitro selection experiments have produced nucleic acid ligands (aptamers) that bind tightly and specifically to a great variety of target biomolecules, The utility of aptamers is often limited by their vulnerability to nucleases present in biological materials, One way to circumvent this problem is to select an aptamer that binds the enantiomer of the target, then synthesize the enantiomer of the aptamer as a nuclease-insensitive ligand of the normal target, We have so identified a mirror-image single-stranded DNA that binds the peptide hormone vasopressin and have demonstrated its stability to nucleases and its bioactivity as a vasopressin antagonist in cell culture.
引用
收藏
页码:11285 / 11290
页数:6
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