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Improvement of a miRNA inhibitor by intracellular selection
Sequences surrounding the miRNA binding domain of the miRNA inhibitor LidNA were selected intracellularly. The library was transfected into cells, and then, inhibitors that were associated with argonaute 2 were selected. The potent inhibitors were slowly degraded intracellularly, while the lower-act...
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Published in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2020-07, Vol.84 (7), p.1451-1454 |
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container_title | Bioscience, biotechnology, and biochemistry |
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description | Sequences surrounding the miRNA binding domain of the miRNA inhibitor LidNA were selected intracellularly. The library was transfected into cells, and then, inhibitors that were associated with argonaute 2 were selected. The potent inhibitors were slowly degraded intracellularly, while the lower-activity inhibitors were rapidly degraded. A combination of the selected sequences surrounding the miRNA binding domain enhanced miRNA inhibitory activity.
LidNA: DNA that puts a lid on miRNA function; LNA: locked nucleic acid; Ago2: argonaute 2; LNA: locked nucleic acid |
doi_str_mv | 10.1080/09168451.2020.1743167 |
format | article |
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source | Oxford Journals Online; EZB Electronic Journals Library |
subjects | Ago2 Argonaute Proteins - metabolism Base Sequence DNA Probes - chemistry DNA Probes - genetics DNA Probes - pharmacology DNA, Single-Stranded - chemistry DNA, Single-Stranded - metabolism HEK293 Cells Humans LidNA MicroRNAs - antagonists & inhibitors MicroRNAs - genetics MicroRNAs - metabolism miRNA miRNA inhibitor Oligonucleotides - pharmacology RNA-Binding Motifs Transfection |
title | Improvement of a miRNA inhibitor by intracellular selection |
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