Brown R S, Lennon J J
Department of Chemistry and Biochemistry, Utah State University, Logan 84322-0300, USA.
Anal Chem. 1995 Jul 1;67(13):1998-2003. doi: 10.1021/ac00109a015.
A linear time-of-flight mass spectrometer has been modified to incorporate pulsed ion extraction of matrix-assisted laser desorption/ionization (MALDI) generated ions. A unique aspect of the experiments presented is the combination of pulsed extraction with very high source potentials (up to 25 kV) which allows improved mass resolution while maintaining excellent sensitivity for the large m/z ions generated by the MALDI technique. Mass resolution in excess of 1000 (fwhm) is demonstrated for cytochrome c (12,361.1 Da) with the pulsed ion extraction linear time-of-flight mass spectrometer described. The influence on obtainable mass resolution of experimental variables such as delay time between laser ionization and ion extraction, amplitude of the pulsed voltage employed, and the source bias voltage are presented. It is shown that, for any given source potential, the optimum pulsed extraction voltage is a linear function of the mass of the analyte. This is consistent with the observation that the initial ion velocity distribution for MALDI-generated ions is independent of mass.
一台线性飞行时间质谱仪已被改装,以纳入对基质辅助激光解吸/电离(MALDI)产生的离子进行脉冲离子提取。本文所展示实验的一个独特之处在于将脉冲提取与非常高的源电势(高达25 kV)相结合,这在保持对MALDI技术产生的大m/z离子具有出色灵敏度的同时,还能提高质量分辨率。使用所描述的脉冲离子提取线性飞行时间质谱仪,细胞色素c(12361.1 Da)的质量分辨率超过了1000(半高宽)。文中展示了诸如激光电离与离子提取之间的延迟时间、所采用的脉冲电压幅度以及源偏置电压等实验变量对可获得的质量分辨率的影响。结果表明,对于任何给定的源电势,最佳脉冲提取电压是分析物质量的线性函数。这与MALDI产生的离子的初始离子速度分布与质量无关这一观察结果是一致的。