Department of Chemistry, University at Albany, State University of New York, 1400 Washington Ave., Albany, NY, 1222, USA.
The RNA Institute, University at Albany State University of New York, 1400 Washington Ave., Albany, NY, 1222, USA.
Chemistry. 2021 Jun 4;27(32):8372-8379. doi: 10.1002/chem.202100742. Epub 2021 May 7.
A new family of hydrazone modified cytidine phosphoramidite building block was synthesized and incorporated into oligodeoxynucleotides to construct photoswitchable DNA strands. The E-Z isomerization triggered by the irradiation of blue light with a wavelength of 450 nm was investigated and confirmed by H NMR spectroscopy and HPLC in the contexts of both nucleoside and oligodeoxynucleotide. The light activated Z form isomer of this hydrazone-cytidine with a six-member intramolecular hydrogen bond was found to inhibit DNA synthesis in the primer extension model by using Bst DNA polymerase. In addition, the hydrazone modification caused the misincorporation of dATP together with dGTP into the growing DNA strand with similar selectivity, highlighting a potential G to A mutation. This work provides a novel functional DNA building block and an additional molecular tool that has potential chemical biology and biomedicinal applications to control DNA synthesis and DNA-enzyme interactions using the cell friendly blue light irradiation.
一种新型腙修饰的胞苷磷酰胺核苷单元被合成并整合到寡脱氧核苷酸中,以构建光致变色 DNA 链。通过 1 H NMR 光谱和 HPLC 在核苷和寡脱氧核苷酸两种情况下,研究并证实了该腙-胞苷在 450nm 蓝光照射下的 E-Z 异构化。发现在六元分子内氢键的作用下,这种腙-胞苷的光激活 Z 型异构体可以抑制 Bst DNA 聚合酶在引物延伸模型中的 DNA 合成。此外,腙修饰导致 dATP 与 dGTP 一起错误地掺入到生长的 DNA 链中,具有相似的选择性,突出了潜在的 G 到 A 突变。这项工作提供了一种新型的功能性 DNA 构建模块和一个额外的分子工具,具有潜在的化学生物学和生物医学应用,可利用细胞友好的蓝光照射来控制 DNA 合成和 DNA-酶相互作用。