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DNA聚合酶对带正电荷的2',3'-双脱氧核苷-5'-三磷酸的有效掺入及其在“直接加载”DNA测序中的应用。

Efficient incorporation of positively charged 2', 3'-dideoxynucleoside-5'-triphosphates by DNA polymerases and their application in 'direct-load' DNA sequencing.

作者信息

Finn Patrick J, Bull Matthew G, Xiao Haiguang, Phillips Paula D, Nelson John R, Grossmann Greg, Nampalli Satyam, McArdle Bernard F, Mamone J Anthony, Flick Parke K, Fuller Carl W, Kumar Shiv

机构信息

Amersham Biosciences, 800 Centennial Avenue, Piscataway, NJ 08855-1327, USA.

出版信息

Nucleic Acids Res. 2003 Aug 15;31(16):4769-78. doi: 10.1093/nar/gkg669.

Abstract

A series of charge-modified, dye-labeled 2', 3'-dideoxynucleoside-5'-triphosphates have been synthesized and evaluated as reagents for dye-terminator DNA sequencing. Unlike the commonly used dye-labeled terminators, these terminators possess a net positive charge and migrate in the opposite direction to dye-labeled Sanger fragments during electrophoresis. Post-sequencing reaction purification is not required to remove unreacted nucleotide or associated breakdown products prior to electrophoresis. Thus, DNA sequencing reaction mixtures can be loaded directly onto a separating medium such as a sequencing gel. The charge-modified nucleotides have also been shown to be more efficiently incorporated by a number of DNA polymerases than regular dye-labeled dideoxynucleotide terminators or indeed normal dideoxynucleoside-5'-triphosphates.

摘要

一系列电荷修饰的、染料标记的2',3'-双脱氧核苷-5'-三磷酸已被合成并作为染料终止子DNA测序试剂进行评估。与常用的染料标记终止子不同,这些终止子带有净正电荷,在电泳过程中与染料标记的桑格片段向相反方向迁移。在电泳前不需要进行测序后反应纯化以去除未反应的核苷酸或相关降解产物。因此,DNA测序反应混合物可以直接加载到分离介质上,如测序凝胶。还表明,与常规染料标记的双脱氧核苷酸终止子或实际上的正常双脱氧核苷-5'-三磷酸相比,电荷修饰的核苷酸能更有效地被多种DNA聚合酶掺入。

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