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Poly(ethylene glycol)-oligodeoxyribonucleotide block copolymers for affinity capillary electrophoretic separation of single-stranded DNAs with a single-base difference

机译:聚乙二醇-低聚脱氧核糖核苷酸嵌段共聚物,用于亲和毛细管电泳分离具有单碱基差异的单链DNA

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摘要

An affinity capillary electrophoretic method was developed to detect a single-base difference of single-stranded DNA (ssDNA). Poly(ethylene glycol)-oligodeoxyribonucleotide block copolymers (PEG-b-ODN) were prepared for use as a novel affinity ligand. We introduced a running buffer solution of PEG-b-ODN into a capillary tube, and electrophoretically separated a mixture of chemically synthesized 20 mer ssDNA (normal ssDNA) and a single-base-substituted 20 mer ssDNA (mutant ssDNA). When the base sequence of PEG-b-ODN was designed to be complementary to part of the normal ssDNA, the migration rate of the normal ssDNA was significantly decreased by reversible hybridization with PEG-b-ODN, depending on the base number of PEG-b-ODN, the salt concentration of the running buffer, and the capillary temperature. In contrast, the mobility of mutant ssDNA did not change because the interaction with PEG-b-ODN was negligible. Optimization of the analytical conditions gave two distinct peaks, one for normal and the other for mutant ssDNA, on the electropherogram, allowing for facile discrimination of the single-base difference. The results indicate that PEG-b-ODN is a promising affinity ligand for the capillary electrophoretic separation of normal and single-base mutated ssDNA.
机译:开发了一种亲和毛细管电泳方法来检测单链DNA(ssDNA)的单碱基差异。制备了聚(乙二醇)-寡脱氧核糖核苷酸嵌段共聚物(PEG-b-ODN),用作新型亲和配体。我们将运行中的PEG-b-ODN缓冲溶液引入毛细管,并电泳分离了化学合成的20 mer ssDNA(正常ssDNA)和单碱基取代的20 mer ssDNA(突变ssDNA)的混合物。当将PEG-b-ODN的碱基序列设计为与部分正常ssDNA互补时,通过与PEG-b-ODN的可逆杂交,正常ssDNA的迁移速率会大大降低,具体取决于PEG-b-ODN的碱基数量b-ODN,运行缓冲液的盐浓度和毛细管温度。相反,突变体ssDNA的迁移率没有变化,因为与PEG-b-ODN的相互作用可忽略不计。分析条件的优化在电泳图谱上给出了两个不同的峰,一个峰为正常峰,另一个峰为突变体ssDNA,可以轻松区分单碱基差异。结果表明,PEG-b-ODN是有希望的亲和配体,用于正常和单碱基突变ssDNA的毛细管电泳分离。

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