National Centre for Mass Spectrometry, Indian Institute of Chemical Technology, Hyderabad, India.
PLoS One. 2012;7(4):e35920. doi: 10.1371/journal.pone.0035920. Epub 2012 Apr 27.
Studies on ligand interaction with quadruplex DNA, and their role in stabilizing the complex at concentration prevailing under physiological condition, has attained high interest. Electrospray ionization mass spectrometry (ESI-MS) and spectroscopic studies in solution were used to evaluate the interaction of PBD and TMPyP4 ligands, stoichiometry and selectivity to G-quadruplex DNA. Two synthetic ligands from PBD family, namely pyrene-linked pyrrolo[2,1-c][1,4]benzodiazepine hybrid (PBD1), mixed imine-amide pyrrolobenzodiazepine dimer (PBD2) and 5,10,15,20-tetrakis(N-methyl-4-pyridyl)porphyrin (TMPyP4) were studied. G-rich single-stranded oligonucleotide d(5'GGGGTTGGGG3') designated as d(T(2)G(8)), from the telomeric region of Tetrahymena Glaucoma, was considered for the interaction with ligands. ESI-MS and spectroscopic methods viz., circular dichroism (CD), UV-Visible, and fluorescence were employed to investigate the G-quadruplex structures formed by d(T(2)G(8)) sequence and its interaction with PBD and TMPyP4 ligands. From ESI-MS spectra, it is evident that the majority of quadruplexes exist as d(T(2)G(8))(2) and d(T(2)G(8))(4) forms possessing two to ten cations in the centre, thereby stabilizing the complex. CD band of PBD1 and PBD2 showed hypo and hyperchromicity, on interaction with quadruplex DNA, indicating unfolding and stabilization of quadruplex DNA complex, respectively. UV-Visible and fluorescence experiments suggest that PBD1 bind externally where as PBD2 intercalate moderately and bind externally to G-quadruplex DNA. Further, melting experiments using SYBR Green indicate that PBD1 unfolds and PBD2 stabilizes the G-quadruplex complex. ITC experiments using d(T(2)G(8)) quadruplex with PBD ligands reveal that PBD1 and PBD2 prefer external/loop binding and external/intercalative binding to quadruplex DNA, respectively. From experimental results it is clear that the interaction of PBD2 and TMPyP4 impart higher stability to the quadruplex complex.
研究配体与四链体 DNA 的相互作用,以及它们在生理条件下的浓度下稳定复合物的作用,引起了高度关注。电喷雾电离质谱(ESI-MS)和溶液光谱研究用于评估 PBD 和 TMPyP4 配体的相互作用、化学计量和对 G-四链体 DNA 的选择性。研究了来自 PBD 家族的两种合成配体,即吡咯并[2,1-c][1,4]苯并二氮杂卓杂合体(PBD1)、混合亚胺酰胺吡咯苯并二氮杂卓二聚体(PBD2)和 5,10,15,20-四(N-甲基-4-吡啶基)卟啉(TMPyP4)。从四膜虫青光眼端粒区设计的富含 G 的单链寡核苷酸 d(5'GGGGTTGGGG3'),指定为 d(T(2)G(8)),用于与配体相互作用。采用电喷雾质谱(ESI-MS)和光谱方法,如圆二色性(CD)、紫外-可见和荧光,研究 d(T(2)G(8)) 序列形成的 G-四链体结构及其与 PBD 和 TMPyP4 配体的相互作用。从 ESI-MS 光谱中可以明显看出,大多数四链体以具有中心两个到十个阳离子的 d(T(2)G(8))(2)和 d(T(2)G(8))(4)形式存在,从而稳定了复合物。PBD1 和 PBD2 与四链体 DNA 相互作用时,CD 带表现出低和高消光性,分别表明四链体 DNA 复合物的展开和稳定。紫外-可见和荧光实验表明,PBD1 外部结合,而 PBD2 适度嵌入并外部结合到 G-四链体 DNA。此外,使用 SYBR Green 的融解实验表明,PBD1 使四链体展开,而 PBD2 稳定四链体复合物。使用 PBD 配体与 d(T(2)G(8)) 四链体的 ITC 实验表明,PBD1 和 PBD2 分别优先与四链体 DNA 进行外部/环结合和外部/嵌入结合。从实验结果清楚地看出,PBD2 和 TMPyP4 的相互作用赋予四链体复合物更高的稳定性。