Markovitsi Dimitra, Onidas Delphine, Gustavsson Thomas, Talbot Francis, Lazzarotto Elodie
Laboratoire Francis Perrin, CEA/DSM/DRECAM/SPAM, CNRS URA 2453, CEA Saclay, 91191 Gif-sur-Yvette, France.
J Am Chem Soc. 2005 Dec 14;127(49):17130-1. doi: 10.1021/ja054955z.
Absorption of UV radiation by DNA bases is known to induce carcinogenic mutations. The lesion distribution depends on the sequence around the hotspots, suggesting cooperativity between bases. Here we show that such cooperativity may intervene at the very first step of a cascade of events by formation of Franck-Condon states delocalized over several bases and subsequent energy transfer faster than 100 fs. Our study focuses on the double helix poly(dA).poly(dT), whose fluorescence, induced by femtosecond pulses at 267 nm, is probed by the upconversion technique and time-correlated single photon counting, over a large time domain (100 fs to 100 ns). The time-resolved fluorescence decays and fluorescence anisotropy decays are discussed in relation with the steady-state absorption and fluorescence spectra in the frame of exciton theory.
已知DNA碱基对紫外线辐射的吸收会诱发致癌突变。损伤分布取决于热点周围的序列,这表明碱基之间存在协同作用。在此我们表明,这种协同作用可能在一系列事件的第一步就发挥作用,即通过形成在多个碱基上离域的弗兰克 - 康登态以及随后快于100飞秒的能量转移。我们的研究聚焦于双螺旋聚(dA)·聚(dT),通过上转换技术和时间相关单光子计数,在较大的时域(100飞秒至100纳秒)内探测其在267纳米飞秒脉冲激发下的荧光。在激子理论框架内,结合稳态吸收和荧光光谱对时间分辨荧光衰减和荧光各向异性衰减进行了讨论。