期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 14, 页码 4987-4990出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b00610
关键词
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资金
- National Institute of General Medical Sciences of the National Institutes of Health [P20GM103451]
We report a new strategy to regulate microRNAs (miRNAs) biogenesis by using bifunctional small molecules that consist of a pre-miRNA binding unit connected by a linker to a Dicer inhibiting unit. In this effort, fluorescence polarization-based screening was used to identify neomycin as a pre-miR-21 binding ligand. Although neomycin cannot inhibit miR-21 maturation, linking it to the RNase inhibitor 1 forms the bifunctional conjugate 7A, which inhibits the production of miR-21. We expect that this strategy will be applicable to design other molecules for miRNA regulation.
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