Chang Der-Yeou, Lee Chia-Cheng, Shiea Jentaie
Department of Chemistry, National Sun Yat-Sen University, Kaohsiung, Taiwan.
Anal Chem. 2002 Jun 1;74(11):2465-9. doi: 10.1021/ac010788j.
A novel fused-droplet electrospray ionization (FD-ESI) source was developed to generate peptide and protein ions. The sample solution was first ultrasonically nebulized to form fine aerosols. The aerosols were then purged into a glass reaction chamber via nitrogen. Charged methanol droplets were continuously generated through electrospraying the acidic methanol solution from a capillary, which was located at the center of the reaction chamber. As the sample aerosols entered the reaction chamber, they fused with the charged methanol droplets from which electrospray proceeded continuously. The mass spectra of peptide and protein that FD-ESI-MS produced were practically identical to those that conventional ESI-MS produced. However, FD-ESI-MS resulted in an extremely high salt tolerance. Cytochrome c ions were detected in the solutions that contained 10% (w/w; 1.709 M) NaCl or 2.5% (425 mM) NaH2PO4. As with those obtained from the solution that lacked NaCl and NaH2PO4, the width of cytochrome c ion peaks remained nearly unchanged.
一种新型的融合液滴电喷雾电离(FD-ESI)源被开发用于产生肽和蛋白质离子。首先将样品溶液超声雾化以形成细气溶胶。然后通过氮气将气溶胶吹扫到玻璃反应室中。通过从位于反应室中心的毛细管电喷雾酸性甲醇溶液连续产生带电的甲醇液滴。当样品气溶胶进入反应室时,它们与带电的甲醇液滴融合,电喷雾从该甲醇液滴中持续进行。FD-ESI-MS产生的肽和蛋白质的质谱与传统ESI-MS产生的质谱几乎相同。然而,FD-ESI-MS具有极高的耐盐性。在含有10%(w/w;1.709 M)NaCl或2.5%(425 mM)NaH2PO4的溶液中检测到细胞色素c离子。与从不含NaCl和NaH2PO4的溶液中获得的离子一样,细胞色素c离子峰的宽度几乎保持不变。