Watching DNA polymerase η make a phosphodiester bond

被引:220
作者
Nakamura, Teruya [1 ,2 ]
Zhao, Ye [1 ,3 ]
Yamagata, Yuriko [2 ]
Hua, Yue-Jin [3 ]
Yang, Wei [1 ]
机构
[1] NIDDKD, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Kumamoto Univ, Grad Sch Pharmaceut Sci, Kumamoto 8620973, Japan
[3] Zhejiang Univ, Inst Nucl Agr Sci, Hangzhou 310029, Zhejiang, Peoples R China
基金
日本学术振兴会; 中国国家自然科学基金; 美国国家卫生研究院;
关键词
CRYSTAL-STRUCTURES; 2-METAL-ION MECHANISM; TERNARY COMPLEXES; TRANSITION-STATE; STRUCTURAL BASIS; ACTIVE-SITE; SUBSTRATE; FIDELITY; METAL; BINDING;
D O I
10.1038/nature11181
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 eta, DNA and dATP were co-crystallized at pH 6.0 without Mg2+. The polymerization reaction was initiated by exposing crystals to 1 mM Mg2+ at pH 7.0, and stopped by freezing at desired time points for structural analysis. The substrates and two Mg2+ 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 Mg2+ ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism.
引用
收藏
页码:196 / U77
页数:7
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