Mass spectrometry via frequency tagging
US-11984311-B2 · May 14, 2024 · US
US12347668B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12347668-B2 |
| Application number | US-202418630314-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 9, 2024 |
| Priority date | Oct 10, 2018 |
| Publication date | Jul 1, 2025 |
| Grant date | Jul 1, 2025 |
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The invention generally relates to mass spectrometry via frequency tagging.
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What is claimed is: 1. A system comprising: a mass spectrometer comprising a single ion trap; and a central processing unit (CPU), and storage coupled to the CPU for storing instructions that when executed by the CPU cause the system to apply a plurality of scan functions to the single ion trap to fragment a precursor ion and simultaneously eject a product ion of the precursor ion in a manner that preserves in time a relationship of the precursor ion and the product ion, wherein the plurality of scan functions comprise a nonlinear AC frequency sweep at constant RF voltage while, simultaneously, the product ion of the precursor ion is ejected from the single ion trap using a time-varying broadband waveform, and wherein fragmentation time of the precursor ion correlates with ejection time of the product ion, allowing the relationship in time to be correlated to the precursor ion mass-to-charge. 2. The system of claim 1 , wherein a value of a mass to charge ratio (m/z) of the precursor ion is directly correlated to fragmentation time. 3. The system of claim 1 , wherein the product ion of the precursor ion is ejected by a scan function that comprises a broadband sum of sines. 4. The system of claim 3 , wherein the broadband sum of sines comprises unevenly spaced frequencies that produce unique beats in a waveform that affect ejection and thus modulate spectral peak shapes. 5. The system of claim 1 , wherein a secular or related frequency of the product ion is directly measured by a detector of the mass spectrometer. 6. The system of claim 1 , wherein the precursor ion is mass-selectively excited via the system applying a nonlinear AC frequency sweep at a constant RF voltage to the single ion trap. 7. The system of claim 1 , wherein the precursor ion is mass-selectively excited via the system applying a fixed AC frequency while the RF voltage is ramped linearly. 8. The system of claim 1 , further comprising an ionization source that allows for high energy ionization of a sample to generate the precursor ion. 9. A system comprising: a mass spectrometer comprising a single ion trap; and a central processing unit (CPU), and storage coupled to the CPU for storing instructions that when executed by the CPU cause the system to apply a plurality of scan functions to the single ion trap to excite a precursor and eject a product ion exactly when the precursor is fragmented, wherein the plurality of scan functions comprise a nonlinear AC frequency sweep at constant RF voltage while, simultaneously, the product ion of the precursor ion is ejected from the single ion trap using a time-varying broadband waveform, and wherein fragmentation time of the precursor ion correlates with ejection time of the product ion, allowing the relationship in time to be correlated to the precursor ion mass-to-charge. 10. A method for analyzing a sample, the method comprising: introducing a precursor ion of a sample into a mass spectrometer comprising a single ion trap; and analyzing the sample via the mass spectrometer that applies a plurality of scan functions to the single ion trap to fragment the precursor ion and simultaneously eject a product ion of the precursor ion in a manner that preserves in time a relationship of the precursor ion and the product ion, wherein the plurality of scan functions comprise a nonlinear AC frequency sweep at constant RF voltage while, simultaneously, the product ion of the precursor ion is ejected from the single ion trap using a time-varying broadband waveform, and wherein fragmentation time of the precursor ion correlates with ejection time of the product ion, allowing the relationship in time to be correlated to the precursor ion mass-to-charge. 11. The method of claim 10 , wherein a value of a mass to charge ratio (m/z) of the precursor ion is directly correlated to fragmentation time. 12. The method of claim 10 , wherein the product ion of the precursor ion is ejected by a scan function that comprises a broadband sum of sines. 13. The method of claim 12 , wherein the broadband sum of sines comprises unevenly spaced frequencies that product unique beats in a waveform that affect ejection and thus modulate spectral peak shapes. 14. The method of claim 10 , wherein a secular or related frequency of the product ion is directly measured by a detector of the mass spectrometer. 15. The method of claim 10 wherein the sample is selected from the group consisting of a biological sample, an industrial sample, an environmental sample, and a pharmaceutical sample. 16. The method of claim 15 , wherein the biological sample comprises a plurality of different components. 17. The method of claim 10 , wherein the sample comprises a plurality of chemical products.
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