Bittl Robert, Weber Stefan
Institut für Experimentalphysik, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany.
Biochim Biophys Acta. 2005 Feb 25;1707(1):117-26. doi: 10.1016/j.bbabio.2004.03.012.
Photogenerated short-lived radical pairs (RP) are common in biological photoprocesses such as photosynthesis and enzymatic DNA repair. They can be favorably probed by time-resolved electron paramagnetic resonance (EPR) methods with adequate time resolution. Two EPR techniques have proven to be particularly useful to extract information on the working states of photoinduced biological processes that is only difficult or sometimes even impossible to obtain by other types of spectroscopy. Firstly, transient EPR yields crucial information on the chemical nature and the geometry of the individual RP halves in a doublet-spin pair generated by a short laser pulse. This time-resolved method is applicable in all magnetic field/microwave frequency regimes that are used for continuous-wave EPR, and is nowadays routinely utilized with a time resolution reaching about 10 ns. Secondly, a pulsed EPR method named out-of-phase electron spin echo envelope modulation (OOP-ESEEM) is increasingly becoming popular. By this pulsed technique, the mutual spin-spin interaction between the RP halves in a doublet-spin pair manifests itself as an echo modulation detected as a function of the microwave-pulse spacing of a two-pulse echo sequence subsequent to a laser pulse. From the dipolar coupling, the distance between the radicals is readily derived. Since the spin-spin interaction parameters are typically not observable by transient EPR, the two techniques complement each other favorably. Both EPR methods have recently been applied to a variety of light-induced RPs in photobiology. This review summarizes the results obtained from such studies in the fields of plant and bacterial photosynthesis and DNA repair mediated by the enzyme DNA photolyase.
光生短寿命自由基对(RP)在光合作用和酶促DNA修复等生物光过程中很常见。利用具有足够时间分辨率的时间分辨电子顺磁共振(EPR)方法可以很好地探测它们。事实证明,两种EPR技术对于提取光诱导生物过程工作状态的信息特别有用,而这些信息通过其他类型的光谱学很难甚至有时根本无法获得。首先,瞬态EPR能提供关于由短激光脉冲产生的双自旋对中单个RP半体的化学性质和几何结构的关键信息。这种时间分辨方法适用于用于连续波EPR的所有磁场/微波频率范围,如今通常以达到约10 ns的时间分辨率使用。其次,一种名为异相电子自旋回波包络调制(OOP-ESEEM)的脉冲EPR方法越来越受欢迎。通过这种脉冲技术,双自旋对中RP半体之间的相互自旋-自旋相互作用表现为一种回波调制,该调制是在激光脉冲之后作为双脉冲回波序列的微波脉冲间距的函数检测到的。根据偶极耦合,可以很容易地得出自由基之间的距离。由于自旋-自旋相互作用参数通常无法通过瞬态EPR观察到,这两种技术相互补充得很好。最近,这两种EPR方法都已应用于光生物学中各种光诱导的RP。这篇综述总结了在植物和细菌光合作用以及由酶DNA光解酶介导的DNA修复领域中此类研究获得的结果。