González-Pérez Alfredo, Dias Rita S, Nylander Tommy, Lindman Björn
Physical Chemistry 1, Centre for Chemistry and Chemical Engineering, Lund University, P.O. Box 124, 22100 Lund, Sweden.
Biomacromolecules. 2008 Mar;9(3):772-5. doi: 10.1021/bm7012907. Epub 2008 Feb 8.
In the present work, we show a new approach for decompaction of DNA-cationic surfactant complexes, e.g., lipoplexes, by using beta-cyclodextrin (beta-CD). The DNA decompaction was achieved by dissolving the surfactant aggregates in the complex by making use of the high affinity between the beta-CD and the free surfactant in solution. The results from fluorescence microscopy and adiabatic compressibility measurements indicate that coils and globules do not coexist. The reported procedure using beta-CD is an efficient way to decompact DNA surfactant complexes because the association constant of surfactants with beta-CD is large. The surfactant's interaction with beta-CD is specific and the nonspecific interaction between beta-CD and biological interfaces is small.
在本研究中,我们展示了一种通过使用β-环糊精(β-CD)来解压缩DNA-阳离子表面活性剂复合物(如脂质体)的新方法。通过利用β-CD与溶液中游离表面活性剂之间的高亲和力,将复合物中的表面活性剂聚集体溶解,从而实现了DNA的解压缩。荧光显微镜和绝热压缩性测量结果表明,线圈状和球状结构并不共存。所报道的使用β-CD的方法是解压缩DNA表面活性剂复合物的有效途径,因为表面活性剂与β-CD的缔合常数很大。表面活性剂与β-CD的相互作用具有特异性,且β-CD与生物界面之间的非特异性相互作用较小。