Grant Gian Paola G, Qin Peter Z
Department of Chemistry, University of Southern California, LJS-251, 840 Downey Way, Los Angeles, CA 90089-0744, USA.
Nucleic Acids Res. 2007;35(10):e77. doi: 10.1093/nar/gkm240. Epub 2007 May 21.
In site-directed spin labeling (SDSL), a nitroxide moiety containing a stable, unpaired electron is covalently attached to a specific site within a macromolecule, and structural and dynamic information at the labeling site is obtained via electron paramagnetic resonance (EPR) spectroscopy. Successful SDSL requires efficient site-specific incorporation of nitroxides. Work reported here presents a new method for facile nitroxide labeling at the 5' terminus of nucleic acids of arbitrary sizes. T4-polynucleotide kinase was used to enzymatically substitute a phosphorothioate group at the 5' terminus of a nucleic acid, and the resulting phosphorothioate was then reacted with an iodomethyl derivative of a nitroxide. The method was successfully demonstrated on both chemically synthesized and naturally occurring nucleic acids. The attached nitroxides reported duplex formation as well as tertiary folding of nucleic acids, indicating that they serve as a valid probe in nucleic acid studies.
在定点自旋标记(SDSL)中,含有稳定未成对电子的氮氧化物部分共价连接到大分子内的特定位点,通过电子顺磁共振(EPR)光谱获得标记位点的结构和动力学信息。成功的SDSL需要高效地将氮氧化物定点掺入。本文报道的工作提出了一种在任意大小核酸的5'末端进行简便氮氧化物标记的新方法。使用T4 - 多核苷酸激酶酶促取代核酸5'末端的硫代磷酸酯基团,然后使所得的硫代磷酸酯与氮氧化物的碘甲基衍生物反应。该方法在化学合成的核酸和天然存在的核酸上均得到成功验证。连接的氮氧化物报告了核酸的双链形成以及三级折叠,表明它们可作为核酸研究中的有效探针。