Guenther Dale C, Karmakar Saswata, Hrdlicka Patrick J
Department of Chemistry, University of Idaho, 875 Perimeter Dr, Moscow, ID 83844-2343, USA.
Chem Commun (Camb). 2015 Oct 18;51(81):15051-4. doi: 10.1039/c5cc06264k.
Double-stranded oligonucleotides with +1 interstrand zipper arrangements of intercalator-functionalized nucleotides are energetically activated for recognition of mixed-sequence double-stranded DNA. Incorporation of nonyl (C9) bulges at specific positions of these probes, results in more highly affine (>5-fold), faster (>4-fold) and more persistent dsDNA recognition relative to conventional Invader probes.
具有嵌入剂功能化核苷酸的 +1 链间拉链排列的双链寡核苷酸在能量上被激活,用于识别混合序列双链 DNA。在这些探针的特定位置引入壬基(C9)凸起,相对于传统的入侵探针,可实现更高亲和力(>5 倍)、更快速度(>4 倍)和更持久的双链 DNA 识别。