首页> 外文期刊>Chemistry: A European journal >Role of Environmental Factors on the Structure and Spectroscopic Response of 5’-DNA–Porphyrin Conjugates Caused by Changes in the Porphyrin-Porphyrin Interactions
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Role of Environmental Factors on the Structure and Spectroscopic Response of 5’-DNA–Porphyrin Conjugates Caused by Changes in the Porphyrin-Porphyrin Interactions

机译:环境因素在由卟啉-卟啉相互作用变化引起的5′-DNA-卟啉缀合物的结构和光谱响应中的作用

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We have explored the utility,strength, and limitation of throughspace exciton-coupled circular dichroism in determination of the secondary structure of optically active chromophoric nanoarrays using the example of end-capped porphyrin– and metalloporphyrin-oligodeoxynucleotide conjugates.We put special emphasis on the explanation of the origin and significance of the distinctive multiple bands in the CD spectra (trisignate and tetrasignate CD bands). Such CD profiles are often observed in chiral aggregates or multichromophoric arrays but have never before been studied in detail. We found that variation of temperature and ionic strength has a profound effect on the geometry of the porphyrin-DNA conjugates and thus the nature of electronic interactions. At lower temperatures and in the absence of NaCl all three 5’-DNA–porphyrin conjugates display negative bisignate CD exciton couplets of variable intensity in the Soret region resulting from through-space interaction between the electric transition dipole moments of the two end-capped porphyrins. As the temperature is raised these exciton couplets are transformed into single positive bands originating from the porphyrin–single-strand DNA interactions. At higher ionic strengths and low temperatures, multisignate CD bands are observed in the porphyrin Soret region. These CD signature bands originate from a combination of intermolecular, end-to-end porphyrin–porphyrin stacking between duplexes and porphyrin– DNA interactions. The intermolecular aggregation was confirmed by fluorescence and absorption spectroscopy and resonance light scattering. DeVoe theoretical CD calculations, in conjunction with molecular dynamics simulations and Monte Carlo conformational searches, were used to mimic the observed bisignate exciton-coupled CD spectra as well as multiple CD bands. Calculations correctly predicted the sign and shape of the experimentally observed CD spectra. These studies reveal that the exciton-coupled circular dichroism is a very useful technique for the determination of the structure of optically active arrays.
机译:我们以封端的卟啉-金属卟啉-寡脱氧核苷酸缀合物为例,探讨了空间激子耦合圆二色性在确定光学活性发色纳米阵列的二级结构中的用途,强度和局限性。我们特别强调了解释CD谱中独特的多个谱带(三标志和四标志CD谱带)的起源和重要性。通常在手性聚集体或多发色性阵列中观察到此类CD谱,但从未进行过详细研究。我们发现,温度和离子强度的变化对卟啉-DNA缀合物的几何形状以及电子相互作用的性质都具有深远的影响。在较低的温度下和没有NaCl的情况下,所有三种5'-DNA-卟啉共轭物在Soret区显示出强度不同的负双信号CD激子对,这是由于两个封端的卟啉的电跃迁偶极矩之间的空间相互作用引起的。 。随着温度的升高,这些激子对转化为源自卟啉-单链DNA相互作用的单个正带。在较高的离子强度和低温下,在卟啉Soret区观察到多符号CD带。这些CD标记带源自双链体之间分子间,端到端的卟啉-卟啉堆积以及卟啉-DNA相互作用的组合。通过荧光和吸收光谱以及共振光散射确认了分子间的聚集。 DeVoe的理论CD计算,结合分子动力学模拟和Monte Carlo构象搜索,用于模拟观察到的双信号激子耦合的CD光谱以及多个CD谱带。计算正确地预测了实验观察到的CD光谱的符号和形状。这些研究表明,激子耦合的圆二色性是确定光学活性阵列结构的非常有用的技术。

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