期刊
CHEMICAL COMMUNICATIONS
卷 57, 期 20, 页码 2487-2490出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc00553g
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资金
- JSPS KAKENHI [JP16K14029, JP18H02081, JP26248016, JP16H06509]
Metal-responsive triplex-forming oligonucleotides incorporating 5-hydroxyuracil nucleobases were synthesized, showing reversible regulation of binding to target natural DNA duplexes by the addition and removal of Gd-III ions under isothermal conditions.
Metal-responsive triplex-forming oligonucleotides (TFOs) were synthesised by incorporating 5-hydroxyuracil (UOH) nucleobases as metal recognition sites. Binding of the UOH-containing TFO to the target natural DNA duplexes was reversibly regulated by the addition and removal of Gd-III ions under isothermal conditions.
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