Bruenner B A, Yip T T, Hutchens T W
Department of Food Science and Technology, University of California, Davis 95616, USA.
Rapid Commun Mass Spectrom. 1996;10(14):1797-801. doi: 10.1002/(SICI)1097-0231(199611)10:14<1797::AID-RCM754>3.0.CO;2-5.
Quantitative aspects of oligonucleotide analysis by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry remain largely unexplored relative to the efforts that have been devoted to quantitative peptide and protein analysis. The successful quantitation of these other biopolymers coupled with the potential of rapid nucleic acid analysis by desorption/ionization techniques prompted the present investigation into quantifying mixed base oligonucleotides of intermediate molecular weights. This report describes the concentration-dependent desorption/ionization of a 21-base oligonucleotide (MW 6361) using a 36-base oligonucleotide (MW 11 131) as an internal standard. Peak height and peak area ratios (analyte to internal standard) varied linearly as a function of oligonucleotide concentration (R2 = 0.966 and 0.991, respectively). The linearity of response extended over nearly three orders of magnitude, from 0.125 to 100 pmol of analyte applied. The use of an internal standard improved the linearity of the calibration curve and reduced relative standard deviations. These results demonstrate for the first time the quantitation of medium size oligonucleotides using MALDI.
与致力于定量肽和蛋白质分析的工作相比,基质辅助激光解吸/电离(MALDI)质谱法对寡核苷酸分析的定量方面仍未得到充分探索。这些其他生物聚合物的成功定量,以及解吸/电离技术对核酸进行快速分析的潜力,促使了目前对中等分子量混合碱基寡核苷酸定量的研究。本报告描述了使用一种36碱基寡核苷酸(分子量11131)作为内标,对一种21碱基寡核苷酸(分子量6361)进行浓度依赖性解吸/电离的情况。峰高和峰面积比(分析物与内标)随寡核苷酸浓度呈线性变化(R2分别为0.966和0.991)。响应的线性范围扩展了近三个数量级,从施加的0.125皮摩尔到100皮摩尔分析物。使用内标提高了校准曲线的线性度并降低了相对标准偏差。这些结果首次证明了使用MALDI对中等大小寡核苷酸进行定量。