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Laser desorption/ionization time-of-flight mass spectrometry on sol-gel-derived 2,5-dihydroxybenzoic acid film

机译:溶胶-凝胶衍生的2,5-二羟基苯甲酸膜的激光解吸/电离飞行时间质谱

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This work presents a novel method for direct desorption/ ionization of analytes from sol-gel-derived film. 2,5-Dihydroxy benzoic acid (DHB), a common MALDI matrix, was incorporated into a sol-gel polymeric structure. The sol-gel-derived DHB thin film can assist the mass analysis of analytes by laser desorption/ionization, with a matrix interference-free background in the mass spectra. The sol-gel-derived film can function as an energy absorber during laser irradiation because it contains DHB molecules. Furthermore, laser irradiation with normal laser power (70 -110 muJ) is not likely to generate any background ions from this sol-gel-DHB derived film. The samples were prepared straightforwardly. After a thin film was formed on a Parafilm membrane from the sol-gel-derived DHB solution coating, the sample solution was directly added to the top of the film, for laser desorption/ ionization mass analysis. The analyte signals were homogeneously obtained on the sol-gel-derived DHB film. Experimental results show that the optimum concentrations of DHB incorporated in the sol-gel solution were between 7500 ppm and 10 000 ppm, providing a matrix interference-free background. Analytes, including small proteins, peptides, amino acids, and small organics, were used to demonstrate the effectiveness of the proposed method. However, a higher laser power (> 110 muJ) than normal was required to desorb small proteins from the sol-gel-derived DHB film. Therefore, a few matrix ions desorbed from the thin film were generated during laser irradiation. The detection limit for both small molecules and proteins, using this sol-gel-assisted laser desorption/ ionization (SGALDI) mass spectrometry (MS), was as low as 81 fmol. However, a mass spectrometer with cutoffmass selection could detect 8.1 fmol of cytochrome c. The largest analyte observed by the SGALDI-MS in this study was myoglobin. [References: 30]
机译:这项工作提出了一种新方法,可直接从溶胶-凝胶衍生膜中对分析物进行解吸/电离。 2,5-二羟基苯甲酸(DHB),一种常见的MALDI基质,被引入到溶胶-凝胶聚合物结构中。溶胶-凝胶衍生的DHB薄膜可通过激光解吸/电离辅助分析物的质量分析,并在质谱图中具有无基质干扰的背景。源自溶胶-凝胶的膜由于包含DHB分子,因此可以在激光照射期间用作能量吸收剂。此外,用正常的激光功率(70 -110μJ)进行的激光辐照不可能从该溶胶-凝胶-DHB衍生的薄膜中产生任何背景离子。样品直接制备。从溶胶-凝胶衍生的DHB溶液涂层在Parafilm膜上形成薄膜后,将样品溶液直接添加到膜的顶部,以进行激光解吸/电离质量分析。在源自溶胶-凝胶的DHB膜上均匀地获得分析物信号。实验结果表明,溶胶-凝胶溶液中掺入的DHB的最佳浓度在7500 ppm至10000 ppm之间,提供了无基质干扰的背景。分析物,包括小蛋白质,肽,氨基酸和小有机物,被用来证明该方法的有效性。但是,从溶胶-凝胶衍生的DHB膜中解吸小蛋白质需要比正常人更高的激光功率(> 110μJ)。因此,在激光照射期间产生了从薄膜解吸的一些基质离子。使用这种溶胶-凝胶辅助的激光解吸/电离(SGALDI)质谱(MS),对小分子和蛋白质的检测限均低至81 fmol。但是,具有截止质量选择的质谱仪可以检测到8.1 fmol的细胞色素c。在这项研究中,通过SGALDI-MS观察到的最大分析物是肌红蛋白。 [参考:30]

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