PREDICTING ANTISENSE OLIGONUCLEOTIDE INHIBITORY EFFICACY - A COMPUTATIONAL APPROACH USING HISTOGRAMS AND THERMODYNAMIC INDEXES

被引:80
作者
STULL, RA
TAYLOR, LA
SZOKA, FC
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT PHARM, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT PHARMACEUT CHEM, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, COMP GRAPH LAB, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1093/nar/20.13.3501
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
Antisense oligonucleotides (ASOs) are designed to bind to a specific mRNA and selectively suppress its translation. To facilitate selection of optimal ASO targets, we have developed three thermodynamic indices to evaluate putative structural complexes important in ASO action. These indices are: a secondary structure score (Sscore), which estimates the strength of local mRNA secondary structures at the ASO target site; a duplex score (Dscore), which estimates the DELTA-G(formation) for the ASO:mRNA target sequence duplex;and a competition score (Cscore), which is the difference between the Dscore and the Sscore. We also present two histograms to graphically display these indices from different regions of the mRNA. The indices are compared to the inhibition reported in five studies of ASO-mediated suppression of gene expression. The Dscore is the most consistent predictor of ASO efficacy in four of the five studies (r2 from 0.44 to 0.99), while the results of the fifth study could not be predicted by any thermodynamic or physical index. Thus the Dscores and their histogram may prove useful in selection of ASO targets.
引用
收藏
页码:3501 / 3508
页数:8
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