Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada.
Photochem Photobiol. 2010 Jul-Aug;86(4):844-51. doi: 10.1111/j.1751-1097.2010.00745.x. Epub 2010 May 13.
Trp-DNA adducts resulting from UV irradiation of pyrimidine bases and nucleotides in the presence of tryptophan (Trp) have been the subject of previous research. However, the relative yield of the adducts compared with the UV screening effect of Trp has not been previously considered. To determine whether Trp-DNA adduct formation or absorption "screening" by Trp is the predominant process when DNA solutions are irradiated with UV light in the presence of Trp, we irradiated Trp-containing DNA oligonucleotide solutions with UVC light and incubated aliquots of those solutions with molecular beacons (MBs) to detect the damage. We observed a rapid decay of fluorescence of the MBs for pure DNA solutions, thereby indicating damage. However, in the presence of Trp, the fluorescence decay is prolonged, with time constants that increase exponentially with Trp concentration. The results are discussed in terms of a beneficial in vivo cellular protection rather than harmful adduct formation and suggest a net sacrificial absorption of UV light by Trp which actually protects the DNA from UV damage.
色氨酸(Trp)存在下嘧啶碱基和核苷酸的紫外线照射产生的 Trp-DNA 加合物是之前研究的主题。然而,与 Trp 的紫外线屏蔽效应相比,加合物的相对产率尚未得到考虑。为了确定当含有 Trp 的 DNA 溶液受到紫外线照射时,Trp-DNA 加合物的形成或吸收“屏蔽”是主要过程,我们用 UVC 光照射含有 Trp 的 DNA 寡核苷酸溶液,并将这些溶液的等分试样与分子信标(MBs)孵育以检测损伤。我们观察到纯 DNA 溶液中 MBs 的荧光迅速衰减,从而表明发生了损伤。然而,在 Trp 存在下,荧光衰减延长,时间常数随 Trp 浓度呈指数增长。结果根据有益的体内细胞保护而不是有害的加合物形成进行了讨论,并表明 Trp 实际上通过牺牲性吸收紫外线来保护 DNA 免受紫外线损伤。