Rentzeperis D, Marky L A, Dwyer T J, Geierstanger B H, Pelton J G, Wemmer D E
Department of Chemistry, New York University, New York 10003.
Biochemistry. 1995 Mar 7;34(9):2937-45. doi: 10.1021/bi00009a025.
A combination of circular dichroism spectroscopy, titration calorimetry, and optical melting has been used to investigate the association of the minor groove ligands netropsin and distamycin to the central A3T2 binding site of the DNA duplex d(CGCAAATTGGC).d(GCCAATTTGCG). For the complex with netropsin at 20 degrees C, a ligand/duplex stoichiometry of 1:1 was obtained with Kb approximately 4.3 x 10(7) M-1, delta Hb approximately -7.5 kcal mol-1, delta Sb approximately 9.3 cal K-1 mol-1, and delta Cp approximately 0. Previous NMR studies characterized the distamycin complex with A3T2 at saturation as a dimeric side-by-side complex. Consistent with this result, we found a ligand/duplex stoichiometry of 2:1. In the current study, the relative thermodynamic contributions of the two distamycin ligands in the formation of this side-by-side complex (2:1 Dst.A3T2) were evaluated and compared with the thermodynamic characteristics of netropsin binding. The association of the first distamycin molecule of the 2:1 Dst.A3T2 complex yielded the following thermodynamic profile: Kb approximately 3.1 x 10(7) M-1, delta Hb = -12.3 kcal mol-1, delta Sb = -8 cal K-1 mol-1, and delta Cp = -42 cal K-1 mol-1. The binding of the second distamycin molecule occurs with a lower Kb of approximately 3.3 x 10(6) M-1, a more favorable delta Hb of -18.8 kcal mol-1, a more unfavorable delta Sb of -34 cal K-1 mol-1, and a higher delta Cp of -196 cal K-1 mol-1. The latter term indicates an ordering of electrostricted and structural water molecules by the complexes. These results correlate well with the NMR titrations and are discussed in context of the solution structure of the 2:1 Dst.A3T2 complex.
采用圆二色光谱、滴定热分析和光学熔解相结合的方法,研究了小沟配体纺锤菌素和偏端霉素与DNA双链体d(CGCAAATTGGC).d(GCCAATTTGCG)的中心A3T2结合位点的结合情况。对于在20℃下与纺锤菌素形成的复合物,得到配体/双链体化学计量比为1:1,结合常数Kb约为4.3×10⁷ M⁻¹,焓变ΔHb约为-7.5 kcal mol⁻¹,熵变ΔSb约为9.3 cal K⁻¹ mol⁻¹,热容变化ΔCp约为0。先前的核磁共振研究表明,饱和状态下偏端霉素与A3T2形成的复合物是一种二聚体并排复合物。与该结果一致,我们发现配体/双链体化学计量比为2:1。在本研究中,评估了在形成这种并排复合物(2:1 Dst.A3T2)过程中两个偏端霉素配体的相对热力学贡献,并与纺锤菌素结合的热力学特征进行了比较。2:1 Dst.A3T2复合物中第一个偏端霉素分子的结合产生了以下热力学数据:Kb约为3.1×10⁷ M⁻¹,ΔHb = -12.3 kcal mol⁻¹,ΔSb = -8 cal K⁻¹ mol⁻¹,ΔCp = -42 cal K⁻¹ mol⁻¹。第二个偏端霉素分子的结合发生时,Kb较低,约为3.3×10⁶ M⁻¹,更有利的ΔHb为-18.8 kcal mol⁻¹,更不利的ΔSb为-34 cal K⁻¹ mol⁻¹,更高的ΔCp为-196 cal K⁻¹ mol⁻¹。后一项表明复合物使电收缩和结构水分子有序排列。这些结果与核磁共振滴定结果很好地相关,并在2:1 Dst.A3T2复合物的溶液结构背景下进行了讨论。