Edwards J R, Itagaki Y, Ju J
Laboratory of DNA Sequencing and Chemical Biology, Columbia Genome Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Nucleic Acids Res. 2001 Nov 1;29(21):E104-4. doi: 10.1093/nar/29.21.e104.
Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MS) has been explored widely for DNA sequencing. The major requirement for this method is that the DNA sequencing fragments must be free from alkaline and alkaline earth salts as well as other contaminants for accurately measuring the masses of the DNA fragments. We report here the development of a novel MS DNA sequencing method that generates Sanger-sequencing fragments in one tube using biotinylated dideoxynucleotides. The DNA sequencing fragments that carry a biotin at the 3'-end are made free from salts and other components in the sequencing reaction by capture with streptavidin-coated magnetic beads. Only correctly terminated biotinylated DNA fragments are subsequently released and loaded onto a mass spectrometer to obtain accurate DNA sequencing data. Compared with gel electrophoresis-based sequencing systems, MS produces a very high resolution of DNA-sequencing fragments, fast separation on microsecond time scales, and completely eliminates the compressions associated with gel electrophoresis. The high resolution of MS allows accurate mutation and heterozygote detection. This optimized solid-phase DNA-sequencing chemistry plus future improvements in detector sensitivity for large DNA fragments in MS instrumentation will further improve MS for DNA sequencing.
基质辅助激光解吸电离飞行时间质谱法(MS)已被广泛用于DNA测序。该方法的主要要求是,DNA测序片段必须不含碱金属盐、碱土金属盐以及其他污染物,以便准确测量DNA片段的质量。我们在此报告一种新型的MS DNA测序方法的开发,该方法使用生物素化的双脱氧核苷酸在一管中生成桑格测序片段。通过用链霉亲和素包被的磁珠捕获,3'端带有生物素的DNA测序片段可在测序反应中去除盐和其他成分。随后仅释放正确终止的生物素化DNA片段并加载到质谱仪上,以获得准确的DNA测序数据。与基于凝胶电泳的测序系统相比,MS产生的DNA测序片段分辨率非常高,在微秒时间尺度上快速分离,并且完全消除了与凝胶电泳相关的条带压缩现象。MS的高分辨率允许准确检测突变和杂合子。这种优化的固相DNA测序化学方法以及未来MS仪器中大型DNA片段检测灵敏度的提高将进一步改进MS用于DNA测序的性能。