| Literature DB >> 26827934 |
Pavel Ryumin1, Jeffery Brown2, Michael Morris3, Rainer Cramer4.
Abstract
Liquid matrix-assisted laser desorption/ionization (MALDI) allows the generation of predominantly multiply charged ions in atmospheric pressure (AP) MALDI ion sources for mass spectrometry (MS) analysis. The charge state distribution of the generated ions and the efficiency of the ion source in generating such ions crucially depend on the desolvation regime of the MALDI plume after desorption in the AP-to-vacuum inlet. Both high temperature and a flow regime with increased residence time of the desorbed plume in the desolvation region promote the generation of multiply charged ions. Without such measures the application of an electric ion extraction field significantly increases the ion signal intensity of singly charged species while the detection of multiply charged species is less dependent on the extraction field. In general, optimization of high temperature application facilitates the predominant formation and detection of multiply charged compared to singly charged ion species. In this study an experimental set-up and optimization strategy is described for liquid AP-MALDI MS which improves the ionization efficiency of selected ion species up to 14 times. In combination with ion mobility separation, the method allows the detection of multiply charged peptide and protein ions for analyte solution concentrations as low as 2fmol/μL (0.5μL, i.e. 1fmol, deposited on the target) with very low sample consumption in the low nL-range.Entities:
Keywords: AP-MALDI; Liquid MALDI; Liquid support matrix; MALDI; MALDI-QTOF; Mass spectrometry; Multiply charged ions
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Year: 2016 PMID: 26827934 DOI: 10.1016/j.ymeth.2016.01.015
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608