Lindemann H
J Cancer Res Clin Oncol. 1985;110(2):170-2. doi: 10.1007/BF00402734.
Lambda-DNA and plasmid pBR 322-DNA, respectively, were treated in vitro with increasing amounts of 4-S-ethanolsulfido-cyclophosphamide (CPA-P1). Subsequent digestion with restriction endonuclease Pvu II or Mbo II revealed discrete alterations in the cleavage patterns as compared to the controls, indicating subtle changes in DNA structure due to CPA-P1 interaction. In the case of pBR 322-DNA the CPA-P1 treatment of supercoiled circular DNA was more inhibitory to subsequent digestion as compared to the treatment of linearized plasmid DNA molecules.
分别用逐渐增加剂量的4-S-乙磺酰基环磷酰胺(CPA-P1)对λ-DNA和质粒pBR 322-DNA进行体外处理。与对照相比,随后用限制性内切酶Pvu II或Mbo II消化显示切割模式有明显改变,表明由于CPA-P1相互作用导致DNA结构发生细微变化。就pBR 322-DNA而言,与线性化质粒DNA分子的处理相比,超螺旋环状DNA的CPA-P1处理对随后的消化更具抑制作用。