Department of Chemistry , University of Houston , Houston , Texas 77204 , United States.
Department of Chemistry , University of North Texas , Denton , Texas 76201 , United States.
J Am Chem Soc. 2019 Sep 4;141(35):13739-13743. doi: 10.1021/jacs.9b06447. Epub 2019 Aug 26.
Enzymes like uracil DNA glycosylase (UDG) can achieve ground state destabilization, by polarizing substrates to mimic rare tautomers. On the basis of computed nucleus independent chemical shifts, NICS(1), and harmonic oscillator model of electron delocalization (HOMED) analyses, of quantum mechanics (QM) and quantum mechanics/molecular mechanics (QM/MM) models of the UDG active site, uracil is strongly polarized when bound to UDG and resembles a tautomer >12 kcal/mol higher in energy. Natural resonance theory (NRT) analyses identified a dominant O2 imidate resonance form for residue bound 1-methyl-uracil. This "tautomeric strain" raises the energy of uracil, making uracilate a better than expected leaving group. Computed gas-phase S2 reactions of free and hydrogen bonded 1-methyl-uracil demonstrate the relationship between the degree of polarization in uracil and the leaving group ability of uracilate.
酶如尿嘧啶 DNA 糖基化酶(UDG)可以通过极化底物来模拟罕见的互变异构体,从而达到基态去稳定化。基于量子力学(QM)和量子力学/分子力学(QM/MM)模型的计算原子核独立化学位移、NICS(1)和电子离域的谐振子模型(HOMED)分析,UDG 活性位点的,当与 UDG 结合时,尿嘧啶被强烈极化,并且类似于能量高 12 千卡/摩尔以上的互变异构体。自然共振理论(NRT)分析确定了与结合的 1-甲基尿嘧啶残基结合的 O2 亚氨基共振形式。这种“互变异构应变”会增加尿嘧啶的能量,使尿嘧啶酸成为比预期更好的离去基团。自由和氢键结合的 1-甲基尿嘧啶的气相 S2 反应计算表明,尿嘧啶的极化程度与尿嘧啶酸的离去基团能力之间存在关系。