Adamcik Jozef, Valle Francesco, Witz Guillaume, Rechendorff Kristian, Dietler Giovanni
Laboratoire de Physique de la Matière Vivante, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
Nanotechnology. 2008 Sep 24;19(38):384016. doi: 10.1088/0957-4484/19/38/384016. Epub 2008 Aug 12.
We study the behavior of single-stranded DNA (ssDNA) in the presence of well-known drugs with either an intercalating binding mode, such as daunorubicin, actinomycin D, and chloroquine, or a minor groove binding mode, such as netropsin and berenil, by atomic force microscopy (AFM). At very low salt conditions, ssDNA molecules adopt an unstructured conformation without secondary structures. We observe that under these conditions additions of drugs that bind to double-stranded DNA (dsDNA) promote the formation of secondary structures in ssDNA. Furthermore, with an increase of concentration of the drugs, the extension as well as the thermal stabilization of these hairpins was observed.
我们通过原子力显微镜(AFM)研究了在存在具有嵌入结合模式的知名药物(如柔红霉素、放线菌素D和氯喹)或小沟结合模式的药物(如纺锤菌素和贝尼尔)的情况下单链DNA(ssDNA)的行为。在极低盐条件下,ssDNA分子呈现无二级结构的无规构象。我们观察到,在这些条件下添加与双链DNA(dsDNA)结合的药物会促进ssDNA中二级结构的形成。此外,随着药物浓度的增加,观察到这些发夹结构的伸展以及热稳定性增强。