Chen Lee Chuin, Kinoshita Masato, Noda Masato, Ninomiya Satoshi, Hiraoka Kenzo
Graduate School, Department of Interdisciplinary Research, University of Yamanashi, Kofu, Yamanashi, 400-8511, Japan,
J Am Soc Mass Spectrom. 2015 Jul;26(7):1085-91. doi: 10.1007/s13361-015-1111-4. Epub 2015 Apr 2.
Recently, we reported a new ESI ion source that could electrospray the super-heated aqueous solution with liquid temperature much higher than the normal boiling point (J. Am. Soc. Mass Spectrom. 25, 1862-1869). The boiling of liquid was prevented by pressurizing the ion source to a pressure greater than atmospheric pressure. The maximum operating pressure in our previous prototype was 11 atm, and the highest achievable temperature was 180°C. In this paper, a more compact prototype that can operate up to 27 atm and 250°C liquid temperatures is constructed, and reproducible MS acquisition can be extended to electrospray temperatures that have never before been tested. Here, we apply this super-heated ESI source to the rapid online protein digestion MS. The sample solution is rapidly heated when flowing through a heated ESI capillary, and the digestion products are ionized by ESI in situ when the solution emerges from the tip of the heated capillary. With weak acid such as formic acid as solution, the thermally accelerated digestion (acid hydrolysis) has the selective cleavage at the aspartate (Asp, D) residue sites. The residence time of liquid within the active heating region is about 20 s. The online operation eliminates the need to transfer the sample from the digestion reactor, and the output of the digestive reaction can be monitored and manipulated by the solution flow rate and heater temperature in a near real-time basis.
最近,我们报道了一种新型电喷雾电离(ESI)离子源,它能够对温度远高于正常沸点的过热水溶液进行电喷雾(《美国质谱学会杂志》25, 1862 - 1869)。通过将离子源加压至高于大气压的压力来防止液体沸腾。我们之前的原型机的最大工作压力为11个大气压,可达到的最高温度为180°C。在本文中,构建了一种更紧凑的原型机,其能够在高达27个大气压和250°C的液体温度下运行,并且可重复的质谱采集可以扩展到以前从未测试过的电喷雾温度。在此,我们将这种过热ESI源应用于快速在线蛋白质消化质谱分析。样品溶液在流经加热的ESI毛细管时被快速加热,并且当溶液从加热毛细管的尖端流出时,消化产物在原位被ESI电离。以甲酸等弱酸作为溶液时,热加速消化(酸水解)在天冬氨酸(Asp,D)残基位点具有选择性裂解。液体在活性加热区域内的停留时间约为20秒。在线操作无需将样品从消化反应器中转移出来,并且消化反应的输出可以通过溶液流速和加热器温度几乎实时地进行监测和控制。