High-Throughput Profiling of Peptide-RNA Interactions Using Peptide Microarrays

被引:35
作者
Pai, Jaeyoung [2 ]
Yoon, Taejin [2 ]
Kim, Nam Doo [3 ]
Lee, Im-Soon [4 ]
Yu, Jaehoon [1 ]
Shin, Injae [2 ]
机构
[1] Seoul Natl Univ, Dept Chem & Educ, Seoul 151742, South Korea
[2] Yonsei Univ, Natl Creat Res Ctr Biofunct Mol, Dept Chem, Seoul 120749, South Korea
[3] Daegu Gyeongbuk Med Innovat Fdn, New Drug Dev Ctr, Taegu 706010, South Korea
[4] Konkuk Univ, Dept Biol Sci, Seoul 143701, South Korea
关键词
REV RESPONSIVE ELEMENT; TARGETING RNA; SUBSTRATE-SPECIFICITY; PROTEIN MICROARRAYS; HELICAL PEPTIDES; BINDING-SITE; HAIRPIN RNA; HIV-1; TAT; RRE RNA; COMPLEX;
D O I
10.1021/ja309760g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A rapid and quantitative method to evaluate binding properties of hairpin RNAs to peptides using peptide microarrays has been developed. The microarray technology was shown to be a powerful tool for high-throughput analysis of RNA peptide interactions by its application to profiling interactions between 111 peptides and six hairpin RNAs. The peptide microarrays were also employed to measure hundreds of dissociation constants (K-d) of RNA peptide complexes. Our results reveal that both hydrophobic and hydrophilic faces of amphiphilic peptides are likely involved in interactions with RNA.s. Furthermore, these results also show that most of the tested peptides bind hairpin RNAs with submicromolar K-d values. One of the peptides identified by using this method was found to have good inhibitory activity against TAR-Tat interactions in cells. Because of their great applicability to evaluation of nearly all types of RNA-peptide interactions, peptide microarrays are expected to serve as robust tools for rapid assessment of peptide-RNA interactions and development of peptide ligands against RNA targets.
引用
收藏
页码:19287 / 19296
页数:10
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