Center for Optical, Molecular and Quantum Science, University of Oregon, Eugene, Oregon, USA; email:
Institute of Molecular Biology, University of Oregon, Eugene, Oregon, USA.
Annu Rev Phys Chem. 2023 Apr 24;74:245-265. doi: 10.1146/annurev-physchem-090419-041204. Epub 2023 Jan 25.
The processes of genome expression, regulation, and repair require direct interactions between proteins and DNA at specific sites located at and near single-stranded-double-stranded DNA (ssDNA-dsDNA) junctions. Here, we review the application of recently developed spectroscopic methods and analyses that combine linear absorbance and circular dichroism spectroscopy with nonlinear 2D fluorescence spectroscopy to study the local conformations and conformational disorder of the sugar-phosphate backbones of ssDNA-dsDNA fork constructs that have been internally labeled with exciton-coupled cyanine (iCy3) dimer probes. With the application of these methods, the (iCy3) dimer can serve as a reliable probe of the mean local conformations and conformational distributions of the sugar-phosphate backbones of dsDNA at various critical positions. The results of our studies suggest a possible structural framework for understanding the roles of DNA breathing in driving the processes of protein-DNA complex assembly and function.
基因组表达、调控和修复的过程需要蛋白质和 DNA 直接相互作用,作用的位置在位于单链-双链 DNA(ssDNA-dsDNA)连接点处和附近的特定位置。在这里,我们综述了最近开发的光谱方法的应用和分析,这些方法将线性吸收和圆二色性光谱与非线性二维荧光光谱相结合,用于研究内部用激子耦合的菁染料(iCy3)二聚体探针标记的 ssDNA-dsDNA 叉结构的糖-磷酸骨架的局部构象和构象无序。应用这些方法,(iCy3)二聚体可以作为 dsDNA 糖-磷酸骨架在各种关键位置的局部构象和构象分布的可靠探针。我们的研究结果为理解 DNA 呼吸在驱动蛋白质-DNA 复合物组装和功能过程中的作用提供了一个可能的结构框架。