Mirror-design of L-oligonucleotide ligands binding to L-arginine

被引:165
作者
Nolte, A [1 ]
Klussmann, S [1 ]
Bald, R [1 ]
Erdmann, VA [1 ]
Furste, JP [1 ]
机构
[1] FREE UNIV BERLIN, INST BIOCHEM, D-14195 BERLIN, GERMANY
关键词
in vitro selection; mirror-design; L-RNA; arginine;
D O I
10.1038/nbt0996-1116
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
The high affinity and selectivity of nucleic acid ligands have clearly demonstrated that RNA can be targeted to a variety of molecules. In practice, however, the use of unmodified aptamers is impeded by the low stability of RNA in biological fluids, Here we describe the mirror-design of a stable 38-mer L-oligoribonucleotide ligand that binds to L-arginine. This L-RNA ligand was also able to bind to a short peptide containing the basic region of the human immunodeficiency virus type-1 Tat-protein, The L-RNA ligand displayed the expected stability in human serum, These findings may contribute to the identification of novel diagnostics and pharmaceuticals.
引用
收藏
页码:1116 / 1119
页数:4
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