Chen Cheng-Tai, Chen Yu-Chie
Department of Applied Chemistry, National Chiao Tung University, Hsinchu 300, Taiwan.
Rapid Commun Mass Spectrom. 2004;18(17):1956-64. doi: 10.1002/rcm.1572.
This paper describes a matrix-free method for performing desorption/ionization directly from mesoporous nanocrystalline titania sol-gel thin films, which have good absorption capacity in the ultraviolet (UV) range and can act as assisting materials during UV matrix-assisted laser desorption/ionization mass spectrometric (MALDI-MS) analysis. A high concentration of citrate buffer was added into this system to provide the proton source and to reduce the presence of alkali cation adducts of the analytes. The analyte signals appear uniformly over the whole sample deposition area. Protonated molecules (MH(+) ions) of analytes dominate the titania MALDI mass spectra. Surfactants, peptides, tryptic digest products, and small proteins with molecular weights below ca. 24 000 Da, are observed in the titania MALDI mass spectra. Detection limits for insulin are as low as ca. 2 fmol with mass resolution of ca. 660.
本文描述了一种无基质方法,可直接从介孔纳米晶二氧化钛溶胶 - 凝胶薄膜进行解吸/电离,该薄膜在紫外(UV)范围内具有良好的吸收能力,并且在紫外基质辅助激光解吸/电离质谱(MALDI - MS)分析过程中可作为辅助材料。向该系统中加入高浓度的柠檬酸盐缓冲液,以提供质子源并减少分析物的碱金属阳离子加合物的存在。分析物信号在整个样品沉积区域均匀出现。分析物的质子化分子(MH(+)离子)在二氧化钛MALDI质谱中占主导地位。在二氧化钛MALDI质谱中观察到了表面活性剂、肽、胰蛋白酶消化产物以及分子量低于约24000 Da的小蛋白质。胰岛素的检测限低至约2 fmol,质量分辨率约为660。