Crespo-Hernández Carlos E, de la Harpe Kimberly, Kohler Bern
Department of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, USA.
J Am Chem Soc. 2008 Aug 20;130(33):10844-5. doi: 10.1021/ja802183s. Epub 2008 Jul 23.
Excited states in double-stranded oligonucleotides containing G.C base pairs were studied by femtosecond transient absorption spectroscopy. Relaxation to the electronic ground state occurs about 10 times more slowly in the duplexes and hairpins studied on average than in the individual mononucleotides of G and C. Detection of long-lived excited states in G.C oligonucleotides complements the earlier observation of slow ground-state recovery in A.T DNA, showing that excited states with picosecond lifetimes are formed in DNAs containing either kind of base pair. The results show further that Watson-Crick G.C base pairs in these base-paired and base-stacked duplexes do not enable subpicosecond relaxation to the electronic ground state. A model is proposed in which fluorescent exciton states decay rapidly and irreversibly to dark exciplex states. This model explains the seemingly contradictory observations of femtosecond fluorescence and slower, picosecond recovery of the ground-state population.
通过飞秒瞬态吸收光谱法研究了含有G.C碱基对的双链寡核苷酸中的激发态。在所研究的双链体和发夹结构中,弛豫到电子基态的速度平均比单个G和C单核苷酸慢约10倍。在G.C寡核苷酸中检测到长寿命激发态,补充了早期对A.T DNA中基态恢复缓慢的观察结果,表明在含有任何一种碱基对的DNA中都会形成具有皮秒寿命的激发态。结果进一步表明,这些碱基配对和碱基堆积的双链体中的沃森-克里克G.C碱基对不能使亚皮秒弛豫到电子基态。提出了一个模型,其中荧光激子态迅速且不可逆地衰减为暗激基复合物态。该模型解释了飞秒荧光和基态布居较慢的皮秒恢复这一看似矛盾的观察结果。