Department of Chemistry, Wayne State University, Detroit, Michigan 48202-3929, USA.
Mol Cell Proteomics. 2010 Feb;9(2):362-7. doi: 10.1074/mcp.M900527-MCP200. Epub 2009 Nov 13.
The first example of a matrix-assisted laser desorption/ionization (MALDI) process producing multiply charged mass spectra nearly identical to those observed with electrospray ionization (ESI) is presented. MALDI is noted for its ability to produce singly charged ions, but in the experiments described here multiply charged ions are produced by laser ablation of analyte incorporated into a common MALDI matrix, 2,5-dihydroxybenzoic acid, using standard solvent-based sample preparation protocols. Laser ablation is known to produce matrix clusters in MALDI provided a threshold energy is achieved. We propose that these clusters (liquid droplets) are highly charged, and under conditions that produce sufficient matrix evaporation, ions are field-evaporated from the droplets similarly to ESI. Because of the multiple charging, advanced mass spectrometers with limited mass-to-charge range can be used for protein characterization. Thus, using an Orbitrap mass spectrometer, low femtomole quantities of proteins produce full-range mass spectra at 100,000 mass resolution with <5-ppm mass accuracy and with 1-s acquisition. Furthermore, the first example of protein fragmentation using electron transfer dissociation with MALDI is presented.
首次展示了一种基质辅助激光解吸/电离(MALDI)过程,该过程产生的多电荷质谱与电喷雾电离(ESI)观察到的质谱几乎完全相同。MALDI 以其产生单电荷离子的能力而闻名,但在本文所述的实验中,通过将分析物激光烧蚀到常见的 MALDI 基质 2,5-二羟基苯甲酸中,使用标准基于溶剂的样品制备方案来产生多电荷离子。激光烧蚀在达到阈值能量的情况下,已知会在 MALDI 中产生基质团簇。我们提出这些团簇(液滴)是高电荷的,并且在产生足够的基质蒸发的条件下,离子从液滴中通过场蒸发类似于 ESI。由于多电荷,具有有限质量电荷比范围的高级质谱仪可用于蛋白质表征。因此,使用轨道阱质谱仪,低飞摩尔数量的蛋白质在 100,000 质量分辨率下产生全范围质谱,质量精度 <5-ppm,采集时间为 1 秒。此外,还首次展示了使用 MALDI 的电子转移解离进行蛋白质片段化的示例。