State Key Laboratory of Bioelectronics, Southeast University, Nanjing 210096, China.
J Biomed Nanotechnol. 2011 Oct;7(5):640-7. doi: 10.1166/jbn.2011.1327.
An improved technique for single nucleotide mismatch discrimination using immobilized double-stranded DNA probes with a shared-stem hairpin (SH) structure is developed. A hairpin-like double-stranded DNA probe without any chromophore was immobilized on an agarose film-coated slide. The base number of the stem area was increased to 9-19 nt and the entire shared-stem area was included in the hybridization area, in which a mutated nucleotide was introduced in the middle. For the perfect match SH probe, we introduced an inner mismatch in the middle positon of the complementary chain. After the introduction of the inner mismatch, the hybridization ability of the SHP probe with a long stem was enhanced significantly. On the other hand, the mismatch probe was not able to hybridize to the perfect matched target. The annealing properties, specificity and hybridization dynamics of this kind of double-stranded DNA probes immobilized on an agarose film are greatly improved in comparison with those for the linear ones and traditional hairpin-like ones. Collectively we demonstrated that this type of immobilized double-stranded DNA probes had an excellent discrimination ratio for single nucleotide mismatches.
采用具有共享茎发夹 (SH) 结构的固定化双链 DNA 探针,开发了一种用于单核苷酸错配区分的改良技术。将无任何生色团的发夹状双链 DNA 探针固定在琼脂糖膜涂覆的载玻片上。将茎区的碱基数增加到 9-19 nt,并将整个共享茎区包含在杂交区中,其中在中间引入了一个突变核苷酸。对于完美匹配的 SH 探针,我们在互补链的中间位置引入了内部错配。引入内部错配后,长茎 SHP 探针的杂交能力显著增强。另一方面,错配探针无法与完美匹配的靶标杂交。与线性和传统发夹状探针相比,固定在琼脂糖膜上的这种双链 DNA 探针的退火特性、特异性和杂交动力学得到了极大改善。总的来说,我们证明了这种固定化双链 DNA 探针对单核苷酸错配具有优异的区分率。