Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nature. 2012 Jul 11;487(7406):196-201. doi: 10.1038/nature11181.
DNA synthesis has been extensively studied, but the chemical reaction itself has not been visualized. Here we follow the course of phosphodiester bond formation using time-resolved X-ray crystallography. Native human DNA polymerase η, DNA and dATP were co-crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped by freezing at desired time points for structural analysis. The substrates and two Mg(2+) ions are aligned within 40 s, but the bond formation is not evident until 80 s. From 80 to 300 s structures show a mixture of decreasing substrate and increasing product of the nucleotidyl-transfer reaction. Transient electron densities indicate that deprotonation and an accompanying C2'-endo to C3'-endo conversion of the nucleophile 3'-OH are rate limiting. A third Mg(2+) ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism.
DNA 合成已得到广泛研究,但该化学反应本身尚未得到可视化。在这里,我们使用时间分辨 X 射线晶体学来跟踪磷酸二酯键形成的过程。在没有 Mg(2+)的情况下,将天然人 DNA 聚合酶 η、DNA 和 dATP 共结晶在 pH 6.0 下。在 pH 7.0 下将晶体暴露于 1 mM Mg(2+)以启动聚合反应,并在所需时间点冷冻以进行结构分析。底物和两个 Mg(2+)离子在 40 秒内对齐,但直到 80 秒才出现键形成的迹象。在 80 到 300 秒之间的结构显示出核苷酸转移反应中底物减少和产物增加的混合物。瞬态电子密度表明,亲核试剂 3'-OH 的去质子化和伴随的 C2'-endo 到 C3'-endo 转化是限速步骤。第三个 Mg(2+)离子与新键一起到达并稳定中间状态,这可能是双金属离子机制中未被认识到的特征。