Field Desorption (FD) is an ionization method that utilizes the tunneling effect in a high electric field generated between an emitter coated with a sample and an electrode to which a high voltage is applied. It is known as a soft ionization method that provides only molecular weight information because the internal energy given to the sample during ionization is low and fragmentation is unlikely to occur. In FD measurements, the sample-coated emitter is introduced directly to the ion source using a dedicated probe. Therefore, it is possible to measure difficult-to-volatile compounds, polar compounds, thermally unstable compounds, etc., which are difficult to measure with GC-MS. The combination of FD and time-of-flight mass spectrometer (TOFMS) enables calculation of the molecular formula of the measured compound. An overview of FD and sampling technique in the gas chromatograph time-of-flight mass spectrometer JMS-T2000GC AccuTOF™ GC-Alpha are described in MSTips No. 355 and MSTips No. 403.
In this MSTips, we report the results of the analysis of the peptide angiotensin I using FD of the JMS-T2000GC as an example of analysis of a highly polar compound.
Commercially available angiotensin I human acetate salt hydrate was used as the sample (Figure 1). Angiotensin I was prepared to 10 mg/mL using a 0.1% TCA:methanol mixture (1:1). Then, 1 μL each of this sample and 1 mg/mL copper(II) phthalocyanine (α-type) methanol solution (used as a mass drift corrector) were applied to the emitter for measurement. A gas chromatograph time-of-flight mass spectrometer JMS-T2000GC AccuTOF™ GC-Alpha was used for the measurements. An EI/FI/FD combination ion source was used, and FD was used as ionization method. Other detailed measurement conditions are shown in Table 1.
Figure 1 Structural formula of angiotensin I
Table 1 Measurement conditions
MS conditions | |
Spectrometer | JMS-T2000GC AccuTOF™ GC-Alpha (JEOL Ltd.) |
Ion Source | EI/FI/FD combination ion source |
Ionization | FD+ (Cathode Voltage: -10 kV, Emitter Current: 0 mA → 51.2 mA/min →50 mA) |
Mass Range | m/z 50 - 1,600 |
Figure 2 shows the TICC for this measurement. Two peaks were detected; the left peak was derived from angiotensin I, and the right peak was derived from copper phthalocyanine.
Figure 2 Total ion current chromatogram
Figure 3 shows the mass spectrum created from the peak of angiotensin I. The [M+H]+, [M+2H]2+, [M+3H]3+ of angiotensin I were detected (Figure 3). Table 2 shows the elemental composition estimated result of these peaks. The mass error was calculated to be within -1.5 mDa, which is a good value. Furthermore, the isotope pattern of [M+H]+ was roughly the same as the simulation result (Figure 4), indicating that good measurement results were obtained. Essentially, peptides cannot be measured using a GC-MS due to its high polarity. But FD which is a direct MS method can be used for peptides analysis, then molecular formula of the peptide can be easily calculated using a FD-TOFMS system.
Figure 3 Mass spectrum of angiotensin I
Ion Type | Measured m/z | Formula | Calculated m/z | Mass Error [mDa] |
[M+H]+ | 1296.68462 | C62 H90 N17 O14 | 1296.68477 | -0.15 |
[M+2H]2+ | 648.84471 | C62 H91 N17 O14 | 648.84602 | -1.31 |
[M+3H]3+ | 432.89845 | C62 H92 N17 O14 | 432.89977 | -1.32 |
Figure 4 Isotope pattern simulation result of [M+H]+
In this MSTips, we introduced the analysis results of angiotensin I as an analysis example of highly polar compound using FD. As a result of the analysis, it was confirmed that protonated molecule related to molecular weight could be observed, and furthermore, accurate mass could be obtained with good accuracy. These results indicate that FD can be used to analyze highly polar compounds that are difficult to measure by GC-MS.
Chemistry
Food / Plant
Biology / Life science
Related productsJMS-T2000GC AccuTOF™ GC-Alpha High Performance Gas Chromatograph - Time-of-Flight Mass Spectrometer
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Jeol Ltd. published this content on 26 March 2024 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 26 March 2024 06:23:06 UTC.