Influence of secondary structure on kinetics and reaction mechanism of DNA hybridization

被引:98
作者
Chen, Chunlai
Wang, Wenjuan
Wang, Zhang
Wei, Fang
Zhao, Xin Sheng [1 ]
机构
[1] Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Struct Chem Unstable & Stable S, Beijing 100871, Peoples R China
[2] Peking Univ, Dept Chem Biol, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1093/nar/gkm177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hybridization of nucleic acids with secondary structure is involved in many biological processes and technological applications. To gain more insight into its mechanism, we have investigated the kinetics of DNA hybridization/ denaturation via fluorescence resonance energy transfer ( FRET) on perfectly matched and single- base- mismatched DNA strands. DNA hybridization shows nonArrhenius behavior. At high temperature, the apparent activation energies of DNA hybridization are negative and independent of secondary structure. In contrast, when temperature decreases, the apparent activation energies of DNA hybridization change to positive and become structure dependent. The large unfavorable enthalpy of secondary structure melting is compensated for by concomitant duplex formation. Based on our results, we propose a reaction mechanism about how the melting of secondary structure influences the hybridization process. A significant point in the mechanism is that the rate- limiting step switches along with temperature variation in the hybridization process of structured DNA, because the free energy profile of hybridization in structured DNA varies with the variation in temperature.
引用
收藏
页码:2875 / 2884
页数:10
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