Method and device for mass spectrometric analysis of biomolecules using charge transfer dissociation (CTD)
Provided herein are devices, systems, and methods of CTD mass spectrometry analysis of biomolecules.
1. A method comprising:
generating a high energy beam of noble gas cations;
passing the high energy beam of noble gas cations into an ion reaction device, where the ion reaction device is part of a mass spectrometer;
contacting an analyte precursor ion present in the ion reaction device with the high energy beam of noble gas cations to produce analyte ion fragments via charge transfer dissociation.
2. The method of claim 1 , wherein the noble gas cations are cations of helium neon, argon or krypton.
3. The method of claim 1 , wherein the energy of high energy beam of noble gas cations ranges from about 0.1 keV to about 15 keV.
4. The method of claim 3 , wherein the energy is about 6 keV.
5. The method of claim 1 , further comprising the step of ionizing an analyte to form the analyte precursor ion.
6. The method of claim 1 , wherein the analyte molecule has a charge of +1, ≥2+, −1 or ≤−2.
7. The method of claim 6 , wherein the analyte molecule has a charge of +1.
8. The method of claim 1 , further comprising the step of separating the analyte ion fragments based on their mass to charge ratios, collisional cross sections and/or differential mobilites.
9. The method of claim 1 , wherein the analyte precursor ions may be selectively reacted with the reagent cation beam on account of their mass to charge ratios, collisional cross sections and/or differential mobilites.
10. The method of claim 1 , further comprising additionally activating the analyte ion fragments and/or the analyte precursor ions.
11. The method of claim 10 , wherein the step of additionally activating the analyte ion fragments and/or the analyte precursor ions occurs before, after, or simultaneously with the step of contacting an analyte precursor ion present in the ion reaction device with the high energy beam of noble gas cations to produce analyte ion fragments via charge transfer dissociation.
12. The method of claim 1 , wherein the step of additionally the activating ion fragments and/or the analyte precursor ions occurs via a collisional, photo, or electron-based activation method.
13. A mass spectrometer comprising:
a reagent ion source, where the reagent ion source is configured to generate a high energy beam of noble gas cations;
an analyte ion source; and
an ion reaction device, where the ion reaction device is operatively coupled to the reagent ion source and the analyte ion source, and where the ion reaction device is configured to contain analyte precursor ions, analyte fragment ions, reagent ions, and combinations thereof.
14. The mass spectrometer of claim 13 , further comprising an ion selection device, wherein the ion selection device is operatively coupled to the reagent ion source, the analyte ion source, and/or the ion reaction device, and wherein the ion selection device is configured to separate ions based on mass to charge ratios, collision cross sections or differential mobilities.
15. The mass spectrometer of claim 13 , further comprising a detector, wherein the detector is operatively coupled to the ion reaction device and/or the ion selection device, and where the detector is configured to detect analyte ion fragments.
16. The mass spectrometer of claim 13 , wherein the noble gas cations are helium cations, neon cations, argon cations, xenon cations or krypton cations.
17. The mass spectrometer of claim 13 , wherein the high energy beam of ions has an energy of about 0.1 to about 15 keV.
18. The mass spectrometer of claim 13 , further comprising an ion focusing device, where the ion focusing device is operatively coupled to the reagent ion source, analyte ion source, and/or the ion reaction device.
19. The mass spectrometer of claim 18 , wherein the ion focusing device increases the effective flux of the noble gas cations.
20. The mass spectrometer of claim 18 , wherein the ion focusing device increases the efficiency of charge transfer dissociation between the high energy beam of ions and the analyte molecules.