Dai Y, Whittal R M, Li L, Weinberger S R
Department of Chemistry, University of Alberta, Edmonton, Canada.
Rapid Commun Mass Spectrom. 1996;10(14):1792-6. doi: 10.1002/(SICI)1097-0231(199611)10:14<1792::AID-RCM753>3.0.CO;2-N.
A method for accurate mass measurement of oligonucleotides up to a DNA 35-mer based on matrix-assisted laser desorption/ionization (MALDI) mass spectrometry is described. In this method, a time-lag focusing time-of-flight mass spectrometer is used to achieve high mass resolution to resolve adduct ions that often complicate the mass analysis of oligonucleotides. Mass resolutions between 1170 and 1300 (full width at half maximum) for a 17-mer, 23-mer, and 35-mer are obtained using a 1 m linear time-of-flight instrument with a total sample loading of less than 10 pmol. The effects of sample preparation, type of calibrant and matrix used on the accuracy of mass measurement, based on external calibration, are discussed. A sample preparation protocol that forms a thin film of matrix and sample crystals on a MALDI probe is described. It is shown that mass measurement error less than 100 ppm with reproducibility better than +/-60 ppm can be obtained with either proteins or DNA fragments as external calibrants. Accurate mass measurement for a mixture of DNA fragments is also illustrated.
描述了一种基于基质辅助激光解吸/电离(MALDI)质谱法对长达35聚体的寡核苷酸进行精确质量测量的方法。在该方法中,使用延时聚焦飞行时间质谱仪来实现高分辨率,以分辨常常使寡核苷酸质量分析复杂化的加合离子。使用总样品负载量小于10皮摩尔的1米线性飞行时间仪器,对于17聚体、23聚体和35聚体可获得1170至1300(半高宽)之间的质量分辨率。讨论了基于外部校准的样品制备、校准剂类型和所用基质对质量测量准确性的影响。描述了一种在MALDI探针上形成基质和样品晶体薄膜的样品制备方案。结果表明,使用蛋白质或DNA片段作为外部校准剂时,可获得小于100 ppm的质量测量误差,重现性优于±60 ppm。还展示了对DNA片段混合物的精确质量测量。