Smith Scott A, Blake Thomas A, Ifa Demian R, Cooks R Graham, Ouyang Zheng
Department of Chemistry, Purdue University, West Lafayette, IN 47907, USA.
J Proteome Res. 2007 Feb;6(2):837-45. doi: 10.1021/pr060514i.
A novel linear ion trap (LIT) mass spectrometer with dual matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization (ESI) ionization sources has been built in the MALDI-LIT-ESI configuration. The design features two independent ion source/ion optical channels connected to opposite ends of a single mass analyzer. The instrument consists of a commercial MALDI-LIT instrument modified by the addition of a home-built vacuum manifold, ion optical system, control electronics, and programming necessary to couple an atmospheric pressure interface to the commercial instrument. In addition to the added ESI functionality, the capabilities of the system also include simultaneous dual-channel ion introduction and analysis and high-duty cycle electronic switching (<1 s) between ion channels. Analytical and ion chemical applications of the dual-source system are explored. One analytical application is the enhanced protein sequence coverage achieved when using both ESI and MALDI to examine a tryptic digest of a six-protein mixture. The differences in the efficiency with which peptides in a mixture are ionized by the two methods give improved sequence coverage when both are applied. Other analytical applications include the use of the ions from one source as intensity or mass standards for the analyte ions from the other. An ion chemistry application involves the use of energy-resolved tandem mass spectrometry (MS/MS) to seek evidence for the generation of isomeric ions from a particular compound using the two ionization methods. A high level of agreement was achieved between the MS/MS spectra recorded under a variety of conditions after ESI and MALDI ionization; this provides evidence of the reproducibility and internal consistency of data from the dual source instrument. However, each of the peptides examined generated identical populations of structures in the two ionization methods under our conditions which are interpreted as involving slow cooling into the most stable minimum on the potential energy surface.
一台具有双基质辅助激光解吸/电离(MALDI)和电喷雾电离(ESI)电离源的新型线性离子阱(LIT)质谱仪已采用MALDI-LIT-ESI配置构建而成。该设计的特点是有两个独立的离子源/离子光学通道,连接到单个质量分析器的相对两端。该仪器由一台商用MALDI-LIT仪器改装而成,增加了一个自制的真空歧管、离子光学系统、控制电子设备以及将大气压接口与商用仪器耦合所需的编程。除了增加的ESI功能外,该系统的能力还包括同时进行双通道离子引入和分析以及离子通道之间的高占空比电子切换(<1秒)。探索了双源系统的分析和离子化学应用。一个分析应用是在使用ESI和MALDI来检测六种蛋白质混合物的胰蛋白酶消化物时实现了增强的蛋白质序列覆盖。当同时应用这两种方法时,混合物中肽被这两种方法电离的效率差异可提高序列覆盖度。其他分析应用包括将来自一个源的离子用作另一个源的分析物离子的强度或质量标准。一个离子化学应用涉及使用能量分辨串联质谱(MS/MS)来寻找使用这两种电离方法从特定化合物生成异构体离子的证据。在ESI和MALDI电离后在各种条件下记录的MS/MS光谱之间达成了高度一致;这提供了来自双源仪器的数据的可重复性和内部一致性的证据。然而,在我们的条件下,所检测的每种肽在两种电离方法中产生了相同的结构群体,这被解释为涉及缓慢冷却到势能表面上最稳定的最小值。