Akerman B, Tuite E
Department of Physical Chemistry, Chalmers University of Technology, Goteborg, Sweden.
Nucleic Acids Res. 1996 Mar 15;24(6):1080-90. doi: 10.1093/nar/24.6.1080.
Photocleavage of dsDNA by the fluorescent DNA stains oxazole yellow (YO), its dimer YOYO) and the dimer TOTO of thiazole orange (TO) has been investigated as a function of binding ratio. On visible illumination, both YO and YOYO cause single-strand cleavage, with an efficiency that varies with the dye/DNA binding ratio in a manner which can be rationalized in terms of free dye being an inefficient photocleavage reagent and externally bound dye being more efficient than intercalated dye. Moreover, the photocleavage mechanism changes with binding mode. Photocleavage by externally bound dye is, at least partly, oxygen dependent with scavenger studies implicating singlet oxygen as the activated oxygen intermediate. Photocleavage by intercalated dye is essentially oxygen-independent but can be inhibited by moderate concentrations of beta- mercaptoethanol--direct attack on the phosphoribose backbone is a possible mechanism. TOTO causes single-strand cleavage approximately five times less efficiently than YOYO. No direct double-strand breaks (dsb) are detected with YO or YOYO, but in both cases single-strand breaks (ssb) are observed to accumulate to eventually produce double-strand cleavage. With intercalated YO the accumulation occurs in a manner consistent with random generation of strand lesions, while with bisintercalated YOYO the yield of double-strand cleavage (per ssb) is 5-fold higher. A contributing factor is the slow dissociation of the bis-intercalated dimer, which allows for repeated strand-attack at the same binding site, but the observation that the dsb/ssb yield is considerably lower for externally bound than for bis-intercalated YOYO at low dye/DNA ratios indicates that the binding geometry and/or the cleavage mechanism are also important for the high dsb-efficiency. In fact, double-strand cleavage yields with bis-intercalated YOYO are higher than those predicted by simple models, implying a greater than statistical probability for a second cleavage event to occur adjacent to the first (i.e. to be induced by the same YOYO molecule). With TOTO the efficiency of the ssb-accumulation is comparable to that observed with YOYO.
已研究了荧光DNA染料恶唑黄(YO)、其二聚体YOYO以及噻唑橙(TO)的二聚体TOTO对双链DNA的光切割作用与结合比的关系。在可见光照射下,YO和YOYO都会导致单链切割,其效率随染料/DNA结合比而变化,这种变化方式可以根据游离染料是低效的光切割试剂以及外部结合的染料比插入染料更高效来解释。此外,光切割机制随结合模式而变化。外部结合染料的光切割至少部分依赖于氧气,清除剂研究表明单线态氧是活性氧中间体。插入染料的光切割基本上不依赖于氧气,但可被中等浓度的β-巯基乙醇抑制——直接攻击磷酸核糖骨架是一种可能的机制。TOTO导致单链切割的效率比YOYO低约五倍。未检测到YO或YOYO直接产生双链断裂(dsb),但在两种情况下都观察到单链断裂(ssb)积累,最终导致双链切割。对于插入的YO,积累以与链损伤随机产生一致的方式发生,而对于双插入的YOYO,双链切割(每ssb)的产率高5倍。一个促成因素是双插入二聚体的缓慢解离,这允许在同一结合位点重复链攻击,但在低染料/DNA比下,外部结合的YOYO的dsb/ssb产率明显低于双插入的YOYO,这一观察结果表明结合几何结构和/或切割机制对于高dsb效率也很重要。事实上,双插入YOYO的双链切割产率高于简单模型预测的值,这意味着第二次切割事件在第一次切割事件附近发生的概率大于统计概率(即由同一个YOYO分子诱导)。对于TOTO,ssb积累的效率与YOYO观察到的效率相当。