Laser Desorption-Atmospheric Pressure Chemical Ionization Mass Spectrometry for the Analysis of Peptides from Aqueous Solutions

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Abstract
A recently reported ionization method, comprising an infrared (IR) laser pulse to desorb (LD) analyte species, followed by atmospheric pressure chemical ionization (APCI) with a corona discharge (LD-APCI) to effect ionization of the desorbed neutral analyte molecules, is described for the direct analysis of aqueous peptide solutions. The source employs a heated capillary atmospheric pressure (AP) inlet coupled to a quadrupole ion trap mass spectrometer and allows sampling under normal ambient air conditions. By use of the corona discharge, signals of the atmospheric pressure infrared matrix-assisted laser desorption/ionization (AP-IR-MALDI)-generated analyte protonated molecule were enhanced by factors as large as 1400. In addition, the acid modifier trifluoroacetic acid (TFA) was found to improve the AP-IR-MALDI-generated signal by a factor of ∼10, whereas the LD-APCI generated signal yielded a 100-fold increase. In this study, the use of the corona discharge is described to enhance the analyte signal generated via AP-IR-MALDI and, as a tool, to probe the gas-phase neutral molecule population generated by the MALDI process. Finally, through the decoupling of desorption from ionization, implications regarding the application of LD-APCI for the direct analysis of numerous new analyte containing matrixes (e.g., polyacrylamide gel electrophoresis (PAGE), tissue, etc.) are discussed.