Department of Biochemistry and Molecular Biology and Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Biochemistry. 2010 Mar 9;49(9):2018-30. doi: 10.1021/bi902027z.
Interactions of histidine with nucleic acid phosphates and histidine pK(a) shifts make important contributions to many protein-nucleic acid binding processes. To characterize these phenomena in simplified systems, we quantified binding of a histidine-containing model peptide HWKK ((+)NH(3)-His-Trp-Lys-Lys-NH(2)) and its lysine analogue KWKK ((+)NH(3)-Lys-Trp-Lys-Lys-NH(2)) to a single-stranded RNA model, polyuridylate (polyU), by changes in tryptophan fluorescence as a function of salt concentration and pH. For both HWKK and KWKK, equilibrium binding constants, K(obs), and magnitudes of log-log salt derivatives, SK(obs) identical with (partial differential logK(obs)/partial differential log[Na(+)]), decreased with increasing pH in the manner expected for a titration curve model in which deprotonation of the histidine and alpha-amino groups weakens binding and reduces its salt-dependence. Fully protonated HWKK and KWKK exhibit the same K(obs) and SK(obs) within uncertainty, and these SK(obs) values are consistent with limiting-law polyelectrolyte theory for +4 cationic oligopeptides binding to single-stranded nucleic acids. The pH-dependence of HWKK binding to polyU provides no evidence for pK(a) shifts nor any requirement for histidine protonation, in stark contrast to the thermodynamics of coupled protonation often seen for these cationic residues in the context of native protein structure where histidine protonation satisfies specific interactions (e.g., salt-bridge formation) within highly complementary binding interfaces. The absence of pK(a) shifts in our studies indicates that additional Coulombic interactions across the nonspecific-binding interface between RNA and protonated histidine or the alpha-amino group are not sufficient to promote proton uptake for these oligopeptides. We present our findings in the context of hydration models for specific vs nonspecific nucleic acid binding.
组氨酸与核酸磷酸盐的相互作用以及组氨酸的 pK(a) 位移对许多蛋白质-核酸结合过程起着重要作用。为了在简化系统中描述这些现象,我们通过色氨酸荧光变化来定量测定含组氨酸的模型肽 HWKK((+)NH(3)-His-Trp-Lys-Lys-NH(2))及其赖氨酸类似物 KWKK((+)NH(3)-Lys-Trp-Lys-Lys-NH(2))与单链 RNA 模型聚尿嘧啶(polyU)的结合,这一过程随盐浓度和 pH 的变化而变化。对于 HWKK 和 KWKK,平衡结合常数 K(obs)和对数盐导数的大小 SK(obs)相同(logK(obs)对 log[Na(+)]的偏微分),随 pH 的增加而降低,这与质子化的组氨酸和 α-氨基基团去质子化削弱了结合并降低了其对盐的依赖性的滴定曲线模型一致。完全质子化的 HWKK 和 KWKK 在不确定度范围内表现出相同的 K(obs)和 SK(obs),并且这些 SK(obs)值与带正电荷的四元寡肽与单链核酸结合的极限定律聚电解质理论一致。HWKK 与 polyU 结合的 pH 依赖性没有提供 pK(a) 位移的证据,也没有任何要求组氨酸质子化,这与在天然蛋白质结构中经常观察到的这些阳离子残基的耦合质子化热力学形成鲜明对比,其中组氨酸质子化满足特定相互作用(例如盐桥形成)在高度互补的结合界面内。我们的研究中没有 pK(a) 位移表明,在 RNA 和质子化组氨酸或 α-氨基基团之间的非特异性结合界面上的额外库仑相互作用不足以促进这些寡肽吸收质子。我们在特定与非特异性核酸结合的水合模型背景下介绍我们的研究结果。