Finn Patrick J, Sun Lei, Nampalli Satyam, Xiao Haiguang, Nelson John R, Mamone J Anthony, Grossmann Greg, Flick Parke K, Fuller Carl W, Kumar Shiv
Amersham Biosciences, 800 Centennial Avenue, Piscataway, NJ 08855-1327, USA.
Nucleic Acids Res. 2002 Jul 1;30(13):2877-85. doi: 10.1093/nar/gkf387.
A novel series of charge-modified, dye-labeled 2',3'-dideoxynucleoside-triphosphate terminators were synthesized and evaluated as reagents for DNA sequencing. These terminators possess an advantage over existing reagents in that no purification is required to remove unreacted nucleotide or associated breakdown products prior to electrophoretic separation of the sequencing fragments. This obviates the need for a time consuming post-reaction work up, allowing direct loading of DNA sequencing reaction mixtures onto a slab gel. Thermo Sequenase II DNA polymerase poorly incorporates the charge-modified terminators compared with regular dye-labeled terminators. However, extending the linker arm between dye and nucleotide and using a mutant form of a related DNA polymerase can in part mitigate the decrease in substrate efficiency. We also present evidence that these charge-modified terminators can relieve gel compression artefacts when used with dGTP in sequencing reactions.
合成了一系列新型的电荷修饰、染料标记的2',3'-双脱氧核苷三磷酸终止剂,并将其作为DNA测序试剂进行评估。这些终止剂相对于现有试剂具有一个优势,即在对测序片段进行电泳分离之前,无需进行纯化以去除未反应的核苷酸或相关的分解产物。这消除了耗时的反应后处理的需要,允许将DNA测序反应混合物直接加载到平板凝胶上。与常规染料标记的终止剂相比,Thermo Sequenase II DNA聚合酶对电荷修饰的终止剂掺入能力较差。然而,延长染料与核苷酸之间的连接臂并使用相关DNA聚合酶的突变形式可以部分减轻底物效率的降低。我们还提供了证据表明,这些电荷修饰的终止剂在测序反应中与dGTP一起使用时可以减轻凝胶压缩假象。