Senior M, Jones R A, Breslauer K J
Department of Chemistry, Rutgers, State University of New Jersey, New Brunswick 08903.
Biochemistry. 1988 May 17;27(10):3879-85. doi: 10.1021/bi00410a053.
We have employed temperature-dependent UV spectroscopy, circular dichroism (CD), 400-MHz proton nuclear magnetic resonance (NMR), and computer modeling to characterize both structurally and thermodynamically the influence of unpaired, dangling thymidine residues (T) on the thermal stability and melting behavior of two DNA core duplexes. The specific DNA double helices that we have investigated in this work are core duplexes [d(GC)3]2 (I) and [d(CG)3]2 (IV), 3' dangling T derivatives [d[(GC)3TT]]2 (II) and [d[(CG)3TT]]2 (V), and 5' dangling T derivatives [d[TT(GC)3]]2 (III) and [d[TT(CG)3]]2 (VI). Our experimental data allow us to reach the following conclusions: (1) For both core duplexes (I and IV), the addition of dangling T residues on either the 5' or 3' end causes an increase in the optical melting temperature tm. (2) For both core duplexes, 5' dangling T residues induce a greater increase in the optical tm's than 3' dangling T residues. (3) For both cores duplexes, the increase in tm induced by the addition of dangling T residues is enthalpic in origin, with 5' dangling T residues inducing a greater increase in the van't Hoff transition enthalpy than 3' dangling T's. (4) Dangling T residues cause downfield shifts in all of the nonexchangeable aromatic protons of the [d(GC)3]2 core duplex (I), with the 5' T residues inducing the largest shifts. For the most part, this trend does not hold with the [d(CG)3]2 core duplex (IV). (5) For both core duplexes, the addition of dangling T residues causes an increase in the NMR tm's of almost all the nonexchangeable aromatic protons of the core duplex.(ABSTRACT TRUNCATED AT 250 WORDS)
我们采用了温度依赖型紫外光谱、圆二色性(CD)、400兆赫质子核磁共振(NMR)以及计算机建模,从结构和热力学两方面来表征未配对的、悬垂的胸腺嘧啶残基(T)对两条DNA核心双链体热稳定性和熔解行为的影响。我们在这项工作中研究的特定DNA双螺旋结构是核心双链体[d(GC)3]2(I)和[d(CG)3]2(IV)、3'端悬垂T衍生物[d[(GC)3TT]]2(II)和[d[(CG)3TT]]2(V)以及5'端悬垂T衍生物[d[TT(GC)3]]2(III)和[d[TT(CG)3]]2(VI)。我们的实验数据使我们能够得出以下结论:(1)对于两条核心双链体(I和IV),在5'或3'端添加悬垂T残基都会导致光学熔解温度tm升高。(2)对于两条核心双链体,5'端悬垂T残基比3'端悬垂T残基引起的光学tm升高幅度更大。(3)对于两条核心双链体,添加悬垂T残基引起的tm升高源于焓变,5'端悬垂T残基引起的范特霍夫转变焓升高幅度比3'端悬垂T残基更大。(4)悬垂T残基使[d(GC)3]2核心双链体(I)所有不可交换芳香族质子的化学位移向低场移动,5'端T残基引起的位移最大。在很大程度上,这种趋势在[d(CG)3]2核心双链体(IV)中并不成立。(5)对于两条核心双链体,添加悬垂T残基会使核心双链体几乎所有不可交换芳香族质子的NMR tm升高。(摘要截于250词)