Sato Shinobu, Umeda Yuta, Fujii Satoshi, Takenaka Shigeori
†Department of Applied Chemistry, ‡Research Center for Biomicrosensing Technology, and §Department of Bioscience and Bioinformatics, Kyushu Institute of Technology, 1-1 Sensui-cho, Tobata-ku, Kitakyushu, Fukuoka 804-8550, Japan.
Bioconjug Chem. 2015 Mar 18;26(3):379-82. doi: 10.1021/bc500535n. Epub 2015 Feb 20.
Ferrocenylnaphthalene diimide carrying β-cyclodextrin (β-CD), 1, intercalated into double-stranded DNA with a binding affinity of K = (6.6 ± 0.8) × 10(4) M(-1) and a binding site size of n = 4, with a high positive cooperative parameter of ω = 14. β-CD and ferrocene moieties of the compound contributed to the formation of the intermolecular inclusion complex on DNA. Binding of 1 resulted in conversion of the DNA duplex to a rod-like form, which was cleaved upon adamantylamine addition.
携带β-环糊精(β-CD)的二茂铁基萘二酰亚胺1,以K = (6.6 ± 0.8) × 10⁴ M⁻¹的结合亲和力和n = 4的结合位点大小插入双链DNA中,具有ω = 14的高正协同参数。该化合物的β-环糊精和二茂铁部分有助于在DNA上形成分子间包合物。1的结合导致DNA双链体转变为棒状形式,在加入金刚烷胺后会被切割。