Folta-Stogniew E, Russu I M
Department of Molecular Biology and Biochemistry, Wesleyan University, Middletown, Connecticut 06459.
Biochemistry. 1994 Sep 13;33(36):11016-24. doi: 10.1021/bi00202a022.
Proton nuclear magnetic resonance spectroscopy is used to characterize the kinetics and energetics of base-pair opening in two self-complementary DNA dodecamer duplexes: [d(CGCACATGTGCG)]2 and [d(CGCAGATCTGCG)]2. The first dodecamer contains two symmetrical CACA/GTGT motifs; in the second dodecamer, each motif is interrupted by a change of the central C.G base pair to a G.C base pair. The opening rates and the equilibrium constants for formation of the open state of each base pair are obtained from the dependence of the imino proton exchange rates on the concentration of ammonia catalyst. The results indicate that the opening rates of the central three base pairs in the CACA/GTGT motif are 3-8-fold larger than the corresponding ones in the CAGA/GTCT sequence. The activation enthalpies and entropies, and the standard enthalpy and entropy changes for formation of the open state, are obtained from the temperature dependence of the opening rates and equilibrium constants, respectively. The results reveal that enthalpy/entropy compensation exists, for all base pairs in both dodecamers, in activation as well as in the equilibria between closed and open states. As a result, the opening rates and equilibrium constants for opening are maintained, in both dodecamers, within a relatively narrow range of values. Nevertheless, large sequence-induced variations are observed for the activation enthalpies and the standard enthalpy changes for opening. The A.T base pair located between the C.G base pairs in the CACA/GTGT motif has a negative enthalpy change for formation of the activated state during opening. This is the first case in which a negative activation enthalpy is observed for opening of a Watson-Crick base pair in DNA.(ABSTRACT TRUNCATED AT 250 WORDS)
质子核磁共振光谱法用于表征两个自互补DNA十二聚体双链体中碱基对打开的动力学和能量学:[d(CGCACATGTGCG)]2 和 [d(CGCAGATCTGCG)]2。第一个十二聚体包含两个对称的CACA/GTGT基序;在第二个十二聚体中,每个基序的中心C.G碱基对变为G.C碱基对,从而被打断。每个碱基对形成开放状态的打开速率和平衡常数是通过亚氨基质子交换速率对氨催化剂浓度的依赖性获得的。结果表明,CACA/GTGT基序中中心三个碱基对的打开速率比CAGA/GTCT序列中相应的碱基对大3至8倍。打开速率和平衡常数对温度的依赖性分别给出了激活焓和熵,以及形成开放状态的标准焓和熵变。结果表明,两个十二聚体中的所有碱基对在激活过程以及封闭和开放状态之间的平衡中都存在焓/熵补偿。因此,两个十二聚体中打开的速率和平衡常数都保持在相对较窄的值范围内。然而,观察到激活焓和打开的标准焓变存在很大的序列诱导变化。CACA/GTGT基序中位于C.G碱基对之间的A.T碱基对在打开过程中形成激活状态时具有负焓变。这是首次在DNA中观察到沃森-克里克碱基对打开时出现负激活焓的情况。(摘要截短于250字)