Canella K, Peltonen K, Dipple A
Chemistry of Carcinogenesis Laboratory, NCI-Frederick Cancer Research and Development Center, MD 21702-1201.
Carcinogenesis. 1991 Jun;12(6):1109-14. doi: 10.1093/carcin/12.6.1109.
Purine deoxyribonucleoside 3'-phosphates were reacted with the (+)- and (-)-enantiomers of the anti dihydrodiol epoxide of benzo[a]pyrene. Products from cis and trans opening of the epoxide ring were separated by HPLC and they were identified by comparison of their CD spectra with those known for the corresponding nucleoside adducts. Thereafter, the eight known benzo[a]pyrene-purine deoxyribonucleoside-3'-phosphate adducts were postlabeled with [32P]ATP and T4 kinase and the positions of these individual bisphosphates were mapped by TLC. Though all eight adducts migrated to the same general region of the thin layer plates, the four possible adducts from each enantiomeric dihydrodiol epoxide were resolved.
嘌呤脱氧核糖核苷3'-磷酸与苯并[a]芘反式二氢二醇环氧化物的(+)-和(-)-对映体反应。通过高效液相色谱法分离环氧化物环顺式和反式开环的产物,并通过将其圆二色光谱与相应核苷加合物的已知光谱进行比较来鉴定它们。此后,将八种已知的苯并[a]芘-嘌呤脱氧核糖核苷-3'-磷酸加合物用[32P]ATP和T4激酶进行后标记,并通过薄层色谱法绘制这些单个二磷酸酯的位置。尽管所有八种加合物都迁移到薄板的同一大致区域,但每种对映体二氢二醇环氧化物的四种可能加合物得以分离。