Sanford D G, Krugh T R
Nucleic Acids Res. 1985 Aug 26;13(16):5907-17. doi: 10.1093/nar/13.16.5907.
The carcinogen N-acetoxy-2-acetylaminofluorene was reacted with d (CCACGCACC) to form a covalent adduct with attachment at the single guanine. The sample was purified, mixed 1:1 with d (GGTGCGTGG) and studied by thermal denaturation experiments. The Tm for the mixture was 35 +/- 3 degrees C, consistent with duplex formation. The method of continuous variation shows that the modified oligomer, d (CCACGAAFCACC), forms a 1:1 duplex with d (GGTGCGTGG). Circular dichroism spectra also indicate the formation of a duplex and suggest that the modified duplex has a left-handed conformation. Addition of the intercalating drug ethidium alters the CD spectrum of the modified duplex, resulting in a CD spectrum similar to that of ethidium bound to right-handed DNA.
致癌物质N-乙酰氧基-2-乙酰氨基芴与d(CCACGCACC)反应,在单个鸟嘌呤处形成共价加合物。样品经纯化后,与d(GGTGCGTGG)按1:1混合,并通过热变性实验进行研究。混合物的解链温度为35±3℃,与双链体形成一致。连续变化法表明,修饰的寡聚物d(CCACGAAFCACC)与d(GGTGCGTGG)形成1:1双链体。圆二色光谱也表明形成了双链体,并表明修饰的双链体具有左手构象。插入药物溴化乙锭的加入改变了修饰双链体的圆二色光谱,产生了与结合到右手DNA上的溴化乙锭相似的圆二色光谱。