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Laser Desorption Ionization Mass Spectrometry on Porous Silica and Alumina for Peptide Mass Fingerprinting

机译:多孔二氧化硅和氧化铝对肽质量指纹晶体的激光解吸电离质谱

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We investigated a variant of desorption/ionization on porous silicon (DIOS) mass spectrometry [1] utilizing an aqueous suspension of either porous silica gel or porous alumina (pore size of 60 A and 90 A, respectively). Laser desorption/ionization (LDI) from samples directly deposited on a stainless steel surface of a MALDI plate without any inorganic substrates was also achieved. Synthetic peptides designed to cover large sequence diversity constituted our model compounds. Sample preparation, including material conditioning, peptide solubilization and deposition protocol onto standard MALDI plate, as well as ionization source tuning were optimized to perform sensitive reproducible LDI analyses. The addition of either a cationizing agent or an alkali metal scavenger to the sample suspension allowed modification of the ionization output. Comparing hydrophilic silica gel to hydrophobic reversed-phase silica gel as well as increasing material pore size provided further insights into desorption/ionization processes. Furthermore, mixtures of peptides were analyzed to probe the spectral suppression phenomenon when no interfering organic matrix was present [2].
机译:我们研究了在多孔硅(DIOS)质谱[1]利用任一多孔二氧化硅凝胶或多孔氧化铝(60 A和90 A,分别的孔径)的水性悬浮液解吸/电离的变体。从直接沉积在MALDI板的不锈钢表面而没有任何无机基材样品激光解吸/电离(LDI)也实现。旨在覆盖大序列多样性合成肽构成我们的模型化合物。样品制备,包括材料调理,肽溶解和沉积协议在标准MALDI板,以及电离源调谐进行了优化以执行敏感再现的LDI分析。在加入任一的阳离子化剂或碱金属清除剂的样品悬浮液的所允许的电离输出的修改。亲水硅胶疏水反相硅胶进行比较以及增加材料孔隙尺寸提供了进一步的见解解吸/电离过程。此外,肽的混合物进行分析,以探测频谱抑制现象时无干扰的有机基体是本[2]。

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