Marcus Andrew H, Matsika Spiridoula, Heussman Dylan, Sorour Mohammed I, Maurer Jack, Albrecht Claire S, Enkhbaatar Lulu, Herbert Patrick, Kistler Kurt A, von Hippel Peter H
Center for Optical, Molecular and Quantum Science, Department of Chemistry and Biochemistry, University of Oregon, Eugene, Oregon 97403.
Institute of Molecular Biology, Department of Chemistry and Biochemistry, and University of Oregon, Eugene, Oregon 97403.
ArXiv. 2024 Mar 27:arXiv:2403.16251v2.
DNA regulation and repair processes require direct interactions between proteins and DNA at specific sites. Local fluctuations of the sugar-phosphate backbones and bases of DNA (a form of DNA 'breathing') play a central role in such processes. Here we review the development and application of novel spectroscopic methods and analyses - both at the ensemble and single-molecule levels - to study structural and dynamic properties of exciton-coupled cyanine and fluorescent nucleobase analogue dimer-labeled DNA constructs at key positions involved in protein-DNA complex assembly and function. The exciton-coupled dimer probes act as 'sensors' of the local conformations adopted by the sugar-phosphate backbones and bases immediately surrounding the dimer probes. These methods can be used to study the mechanisms of protein binding and function at these sites.
DNA调控和修复过程需要蛋白质与特定位点的DNA之间进行直接相互作用。DNA的糖磷酸骨架和碱基的局部波动(一种DNA“呼吸”形式)在此类过程中起着核心作用。本文综述了新型光谱方法及分析技术在整体和单分子水平上的发展与应用,以研究激子耦合花青和荧光核碱基类似物二聚体标记的DNA构建体在参与蛋白质-DNA复合物组装和功能的关键位置的结构和动力学性质。激子耦合二聚体探针可作为二聚体探针周围紧邻的糖磷酸骨架和碱基所采用的局部构象的“传感器”。这些方法可用于研究这些位点上蛋白质结合和功能的机制。