Froim D, Hopkins C E, Belenky A, Cohen A S
Analytical Research, Hybridon, Inc., Cambridge, MA 02139, USA.
Nucleic Acids Res. 1997 Nov 1;25(21):4219-23. doi: 10.1093/nar/25.21.4219.
The progress of antisense DNA therapy demands development of reliable and convenient methods for sequencing short single-stranded oligonucleotides. A method of phosphorothioate antisense DNA sequencing analysis using UV detection coupled to capillary electrophoresis (CE) has been developed based on a modified chain termination sequencing method. The proposed method reduces the sequencing cost since it uses affordable CE-UV instrumentation and requires no labeling with minimal sample processing before analysis. Cycle sequencing with ThermoSequenase generates quantities of sequencing products that are readily detectable by UV. Discrimination of undesired components from sequencing products in the reaction mixture, previously accomplished by fluorescent or radioactive labeling, is now achieved by bringing concentrations of undesired components below the UV detection range which yields a 'clean', well defined sequence. UV detection coupled with CE offers additional conveniences for sequencing since it can be accomplished with commercially available CE-UV equipment and is readily amenable to automation.
反义DNA疗法的进展需要开发可靠且便捷的短单链寡核苷酸测序方法。基于改良的链终止测序方法,已开发出一种使用紫外检测与毛细管电泳(CE)联用的硫代磷酸酯反义DNA测序分析方法。该方法降低了测序成本,因为它使用价格合理的CE-UV仪器,并且在分析前无需标记且样品处理最少。使用ThermoSequenase进行循环测序可产生大量易于通过紫外检测的测序产物。以前通过荧光或放射性标记来区分反应混合物中测序产物中的不需要成分,现在通过使不需要成分的浓度低于紫外检测范围来实现,从而产生“干净”、明确的序列。紫外检测与CE联用为测序提供了额外的便利,因为它可以使用市售的CE-UV设备完成,并且易于实现自动化。