NUCLEASE-RESISTANT NUCLEIC-ACID LIGANDS TO VASCULAR-PERMEABILITY FACTOR VASCULAR ENDOTHELIAL GROWTH-FACTOR

被引:213
|
作者
GREEN, LS [1 ]
JELLINEK, D [1 ]
BELL, C [1 ]
BEEBE, LA [1 ]
FEISTNER, BD [1 ]
GILL, SC [1 ]
JUCKER, FM [1 ]
JANJIC, N [1 ]
机构
[1] NEXSTAR PHARMACEUT,BOULDER,CO 80301
来源
CHEMISTRY & BIOLOGY | 1995年 / 2卷 / 10期
关键词
ANGIOGENESIS; 2'-AMINO-2'-DEOXYPYRIMIDINE NUCLEOTIDE RNA; COMBINATORIAL LIBRARIES; IN VITRO EVOLUTION; NUCLEASE-RESISTANT OLIGONUCLEOTIDES;
D O I
10.1016/1074-5521(95)90032-2
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
Background: Vascular permeability factor/vascular endothelial growth factor (VPF/VEGF) is a potent inducer of new blood vessel growth (angiogenesis) that contributes to the pathology of many angiogenesis-associated disease states such as psoriasis, rheumatoid arthritis and cancer. Few molecular entities capable of binding to VPF/VEGF with high affinity and specificity have been described to date. Result: Nuclease-resistant 2'-amino-2'deoxypyrimidine nucleotide RNA (2'-aminopyrimidine RNA) ligands that bind to VPF/VEGF with high affinity have been identified by iterative rounds of affinity-selection/amplification from two independent random libraries. The sequence information that confers high affinity binding to VPF/VEGF is contained in a contiguous stretch of 24 nucleotides, 5'-CCCUGAUGGUAGAC-GCCGGGGUG-3' (2'-aminopyrimidine nucleotides are designated with italic letters). Of the 14 ribopurines in this minimal ligand, 10 can be substituted with the corresponding 2'-O-methylpurine nucleotides without a reduction in binding affinity to VPF/VEGE In fact, the 2'O-methyl substitution at permissive positions leads to a similar to 17-fold improvement in the binding affinity to VPF/VEGE. The higher affinity results from the reduction in the dissociation rate constant of the 2'-O-methyl-substituted RNA ligand from the protein compared to the unsubstituted ligand. The 2'-O-methyl-substituted minimal ligand, which folds into a bulged hairpin motif, is also more thermally stable than the unsubstituted ligand. Nuclease resistance of the Ligand is further improved by the 2'-O-methyl substitutions and the addition of short phosphorothioate caps to the 3'- and 5'-ends. Conclusions: We have used the SELEX (systematic evolution of ligands by exponential enrichment) process in conjunction with post-SELEX modifications to define a highly nuclease-resistant oligonucleotide that binds to VPF/VEGF with high affinity and specificity.
引用
收藏
页码:683 / 695
页数:13
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