Mass spectrometer having fragmentation region

Abstract

A mass spectrometer is disclosed comprising: a first vacuum chamber having an inlet aperture; a second vacuum chamber; a differential pumping aperture separating the vacuum chambers; and an ion guide arranged in the first vacuum chamber for guiding ions from the inlet aperture to and through the differential pumping aperture. The ion guide has a construction for handling high gas loads such that the spectrometer is able to maintain the gas pressure in the first vacuum chamber such that when ions are accelerated therethrough the ions collide with gas and fragment.

Claims

1. A method of identifying biomolecules by mass spectrometry comprising: (i) providing a mass spectrometer comprising: a first vacuum chamber having an inlet aperture; a second vacuum chamber adjacent the first vacuum chamber; a differential pumping aperture separating the first and second vacuum chambers; an ion guide arranged in the first vacuum chamber for guiding ions from the inlet aperture to and through the differential pumping aperture, wherein the ion guide comprises a first portion configured to guide ions along a first axial path, a second portion configured to guide ions along a second different axial path, and a transition portion configured to urge ions from the first axial path onto the second axial path; and a voltage supply arranged and configured to apply voltages to electrodes in the spectrometer so as to accelerate ions through the first vacuum chamber; (ii) transmitting ions of said biomolecules through said inlet aperture into said ion guide; (iii) guiding ions through said ion guide along said first axial path, through said transition portion and along said second axial path to said differential pumping aperture; and (iv) operating the spectrometer in a first mode in which the pressure in the first vacuum chamber and said voltage supply are controlled such that the ions are accelerated by the voltage supply so as to collide with gas in the first vacuum chamber and fragment to form fragment ions.

2. The method of claim 1, wherein the biomolecules are peptides.

3. The method of claim 2, comprising identifying the peptides by peptide mapping.

4. The method of claim 2, comprising digesting a protein or peptide and ionising the resulting peptides so as to form peptide ions, and then transmitting the peptide ions through said inlet aperture.

5. The method of claim 4, comprising digesting a monoclonal antibody and ionising the resulting peptides so as to form peptide ions, and then transmitting peptide ions through said inlet aperture.

6. The method of claim 4, comprising separating said resulting peptides before the step of ionising the peptides so that ions of different peptides are transmitted into the ion guide at different times.

7. The method of claim 1, wherein said voltage supply generates a DC voltage gradient in the first vacuum chamber that accelerates the ions to fragment them into said fragment ions; and wherein a range of different DC voltage gradients are provided during a single experimental run.

8. The method of claim 1, wherein the first vacuum chamber is pumped to a first pressure and the second vacuum chamber is pumped to a second, lower pressure.

9. The method of claim 1, wherein the inlet aperture separates the first vacuum chamber from a region that is at higher pressure than the first vacuum chamber and that contains an ion source for generating the ions.

10. The method of claim 1, wherein the inlet aperture has a diameter of: ≥0.5 mm; ≥0.55 mm; ≥0.6 mm; ≥0.65 mm; ≥0.7 mm; ≥0.75 mm; ≥0.8 mm; ≥0.85 mm; ≥0.9 mm; ≥0.95 mm; or ≥1 mm.

11. The method of claim 1, wherein a central axis of the first axial path of the ion guide passes through said inlet aperture and/or wherein a central axis of the first axial path of the ion guide is coaxial with a central axis said inlet aperture.

12. The method of claim 1, wherein a central axis of the second axial path of the ion guide passes through said differential pumping aperture and/or wherein a central axis of the second axial path of the ion guide is coaxial with a central axis said differential pumping aperture.

13. The method of claim 1, comprising evacuating gas from the first vacuum chamber through a gas pumping port, wherein at least part of the second portion of the ion guide is shielded from the gas pumping port by a barrier so that gas flow through the first vacuum chamber passes from said inlet aperture to the gas pumping port without passing through said at least part of the second portion of the ion guide.

14. The method of claim 1, wherein the first vacuum chamber comprises a gas pumping port for evacuating the first vacuum chamber of gas, and wherein a central axis of the first axial path of the ion guide passes through said gas pumping port and/or wherein a central axis of the first axial path of the ion guide is coaxial with a central axis said gas pumping port.

15. The method of claim 1, wherein the first portion of the ion guide has a larger radial cross-section than the second portion of the ion guide.

16. The method of claim 1, comprising mass and/or ion mobility analysing ions in the second vacuum chamber or in a further vacuum chamber downstream of the second vacuum chamber.

17. The method of claim 16, wherein the ions are mass analysed by a Time of Flight mass analyser.

18. The method of claim 1, comprising operating the spectrometer in a second mode in which the pressure in the first vacuum chamber and said voltage supply are controlled such that ions are fragmented at a substantially lower rate than in the first mode.

19. The method of claim 18, comprising mass analysing fragment ions in the first mode, mass analysing precursor ions in second mode, and correlating the fragment ions analysed in the first mode with their respective precursor ions analysed in the second mode.

20. A method of biotherapeutics characterisation or monitoring critical quality attributes comprising: (i) providing a mass spectrometer comprising: a first vacuum chamber having an inlet aperture; a second vacuum chamber adjacent the first vacuum chamber; a differential pumping aperture separating the first and second vacuum chambers; an ion guide arranged in the first vacuum chamber for guiding ions from the inlet aperture to and through the differential pumping aperture, wherein the ion guide comprises a first portion configured to guide ions along a first axial path, a second portion configured to guide ions along a second different axial path, and a transition portion configured to urge ions from the first axial path onto the second axial path; and a voltage supply arranged and configured to apply voltages to electrodes in the spectrometer so as to accelerate ions through the first vacuum chamber; (ii) transmitting ions through said inlet aperture into said ion guide; (iii) guiding ions through said ion guide along said first axial path, through said transition portion and along said second axial path to said differential pumping aperture; and (iv) operating the spectrometer in the first mode in which the pressure in the first vacuum chamber and said voltage supply are controlled such that the ions are accelerated by the voltage supply so as to collide with gas in the first vacuum chamber and fragment to form fragment ions.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Various embodiments will now be described, by way of example only, and with reference to the accompanying drawings in which:

(2) FIG. 1 schematically illustrates part of a known mass spectrometer;

(3) FIG. 2A shows part of a mass spectrometer according to an embodiment of the present invention, FIG. 2B shows cross-sectional views through different portions of the ion guide shown in FIG. 2A, and FIG. 2C shows a perspective view of the transition portion of the ion guide;

(4) FIG. 3 shows the ion current as a function of time for an embodiment of the present invention, in a low fragmentation mode (upper plot) and a high fragmentation mode (lower plot);

(5) FIG. 4 shows the results of a peptide mapping experiment;

(6) FIG. 5 shows MS/MS fragmentation quality of an embodiment of the present invention;

(7) FIG. 6 shows a cross-section through the transition region of an ion guide according to an embodiment wherein the ion guide is formed from stacked plate electrodes; and

(8) FIG. 7 shows a cross-section through the transition region of an ion guide according to an embodiment wherein the ion guide is formed from rod electrodes.

DETAILED DESCRIPTION

(9) In mass spectrometry, analyte ions are often generated by relatively high pressure ion sources, e.g. by atmospheric pressure ion sources. It is then necessary to transmit these ions into a vacuum region of the mass spectrometer, since the processing or analysis of the ions is required to be performed at relatively low vacuum pressures.

(10) FIG. 1 schematically illustrates a known arrangement comprising an electrospray ionisation (ESI) probe 2 arranged in an atmospheric pressure region 4, a low pressure vacuum chamber 6 of a mass spectrometer, and an intermediate pressure chamber 8 arranged between the atmospheric pressure region 4 and the vacuum chamber 6 of the mass spectrometer. A cone 10 is arranged between the atmospheric pressure region 4 and the intermediate pressure chamber 8 so that the intermediate pressure chamber 8 is able to be maintained at a lower pressure than the atmospheric pressure region 4, and a differential pumping aperture 12 is arranged between the vacuum chamber 6 and the intermediate pressure chamber 8 so that the vacuum chamber is able to be maintained at a lower pressure than the intermediate pressure chamber. A multipole ion guide 14 is arranged in the intermediate pressure chamber 8 for guiding ions received through the cone 10 towards and through the differential pumping aperture 12.

(11) In operation, the intermediate pressure chamber 8 is pumped to a lower pressure than the atmospheric pressure region 4, and the vacuum chamber 6 is pumped to a lower pressure than the intermediate pressure chamber 8. Analyte solution is then delivered to the capillary 16 of the ESI probe 2 and is sprayed from the tip thereof so as to produce analyte ions 18 in the atmospheric pressure region 4. The analyte ions 18 then pass through the cone 10 and into the ion guide 14 in the intermediate pressure chamber 8. The ion guide 14 guides the ions through the intermediate pressure chamber and through the differential pumping aperture 12 into the vacuum chamber 6. The ions may then be fragmented in the vacuum chamber 6, or in a further downstream vacuum chamber of the spectrometer which may be pumped to an even lower pressure.

(12) FIG. 2A shows an embodiment of the present invention that is similar to that shown in FIG. 1, except that the multipole rod set ion guide has been replaced by another type of ion guide that guides ions along a first axial path and then onto and along a second axial path that is displaced from the first axial path, and voltages are applied to the instrument so as to accelerate the ions in the background gas so as to cause them to fragment via CID fragmentation.

(13) In the embodiment of FIG. 2A, the sampling cone 20 separates the relatively high pressure region 22 (such as an atmospheric pressure region) from the first vacuum chamber 24. An electrospray ionisation (ESI) probe, or other source of ions, may be arranged in high pressure region 22. A differential pumping aperture 26 is arranged between the first vacuum chamber 24 and a second vacuum chamber 28 so that the second vacuum chamber 28 is able to be maintained at a lower pressure than the first vacuum chamber 24. The ion guide is arranged in the first vacuum chamber 24 for guiding ions received through the sampling cone 20 towards and through the differential pumping aperture 26, as will be described in more detail below. A mass analyser 29, such as an orthogonal acceleration Time of Flight mass analyser, may be arranged in the second vacuum chamber 28 for analysing ions transmitted through the differential pumping aperture 26.

(14) The ion guide comprises a first portion 30 for guiding ions along a first axial path, a second portion 32 for guiding ions along a second axial path (which may be parallel to and displaced the first axial path), and a transition portion 33 for transferring ions from the first axial path to the second axial path. In the depicted embodiment, each of the first and second ion guide portions 20,32 comprises a plurality of axially separated apertured electrodes (e.g. ring electrodes) for radially confining the ions along their respective axial paths. RF voltages are applied to these electrodes so as to radially confine the ions. For example, different (e.g. opposite) phases of an RF voltage supply may be applied to adjacent apertured electrodes in the known manner so as to radially confine the ions.

(15) FIG. 2B shows three cross-sectional views of the electrode arrangement in the ion guide at different axial points along the ion guide. View 30 shows the electrode arrangement proximate the sampling cone 20, where the ions are confined in the first portion 30 of the ion guide to the first axial path by the apertured electrodes 34. View 32 shows the electrode arrangement proximate the differential pumping aperture 26, where the ions are confined in the second portion of the ion guide 32 to the second axial path by the apertured electrodes 35. View 33 shows the electrode arrangement in the transition region 33 of the ion guide, in which the ions are transferred from the first axial path of the first ion guide portion 30 to the second axial path of the second ion guide portion 32. This transfer may be achieved by: providing one or more electrodes 36 in the transition region, each of which only partially encircles the first axial path and has a radial opening in its side that is directed towards the second axial path (e.g. an arc-shaped electrode); providing one or more electrodes 37 in the transition region, each of which only partially encircles the second axial path and has a radial opening in its side that is directed towards the first axial path (e.g. an arc-shaped electrode); and urging ion from the first axial path, through the radial openings in the electrodes, and onto the second axial path. This urging of the ions may be performed by providing an electrical potential difference, e.g. by applying voltages to the electrodes in the transition region so as to provide a potential difference in the radial direction.

(16) FIG. 2C shows a perspective view of the electrode arrangement in the transition region.

(17) Referring back to FIG. 2A, the first ion guide portion 30 may be arranged in the first vacuum chamber 24 such that the aperture of the sampling cone 20 is aligned (e.g. coaxial) with the first axial path defined by the first ion guide portion 30. The second ion guide portion 32 may be arranged in the first vacuum chamber 24 such that the aperture in the differential pumping aperture 26 is aligned (e.g. coaxial) with the second axial path defined by the second ion guide portion 32.

(18) A vacuum pump is provided for evacuating the first vacuum chamber 24 through a gas pumping port 38. The opening of the gas pumping port 38 may be aligned (e.g. coaxial) with the first axial path of the first ion guide portion 30. The end of the ion guide formed by the second portion 32 may be physically shielded from the gas pumping port 38 by a barrier 40.

(19) In operation, ions are generated in high pressure region 22. The pressure differential between the high pressure region 22 and the first vacuum chamber 24 causes gas and ions to pass through the cone 20 and into the first vacuum chamber 24, whereby the gas and ions tend to expand into the lower pressure region. The ions enter into the first portion 30 of the ion guide and are radially confined thereby, but may be relatively diffuse, as shown by ion cloud 42. The ions are driven axially along the first portion 32 of the ion guide, at least partially by the gas flow towards the gas pumping port 38. When ions reach the transition portion 33 of the ion guide, they are urged in the radial direction and onto the second axial path defined by the second portion 32 of the ion guide, as shown by ion trajectories 43. As described above, this may be caused by applying a potential difference in the radial direction. As a result, ions are caused to migrate from the first ion guide portion 30 to the second ion guide portion 32. In contrast, the majority of the gas flow continues substantially along the axis defined by the first ion guide portion 30 towards and through the gas pumping port 38, as shown by arrow 44. Ions are therefore radially confined in the second ion guide portion 32 and travel along the second axial path towards the differential pumping aperture 26, whereas the majority of the gas is routed in a different direction towards the gas pumping port 38. At least part of the second portion 32 of the ion guide may be shielded from the pumping port by a barrier 40, so that the gas flow towards the pumping port 38 is directed away from the second axial path of the second ion guide portion 32.

(20) The second ion guide portion 32 may have a smaller radial cross-section than the first portion 30 so that the ions are radially compressed in the second portion as compared to the first portion, as shown by ion beam 46. Ions are then guided by the second ion guide portion 32 through the differential pumping aperture 26 and into the second vacuum chamber 28.

(21) Ion guides of the type described above are known for converting a diffuse ion cloud into a more compact ion cloud. However, the inventors have recognised that the ion guide in the above-described arrangement is able to handle relatively high gas loads (e.g. since the ion guide initially conveys the ions with the gas flow towards the pumping port and then moves the ions out of the gas flow), and that the ion guide therefore enables the first vacuum chamber 24 to be operated at relatively high pressures such that efficient CID fragmentation may be performed in this region.

(22) Embodiments of the invention therefore accelerate the ions through the gas in the first vacuum chamber 24 so as to cause collisions between the ions and the gas molecules (and other species) that result in CID fragmentation of the precursor ions to form fragment ions. The precursor ions may be accelerated through the gas by a static DC electric field. For example, a DC voltage gradient may be arranged between a point in the first vacuum chamber 24 towards the cone 20 and a point towards the differential pumping aperture 26, e.g. by applying different DC voltages to these elements and/or to electrodes of the ion guide. The DC voltage gradient may be arranged along the first and/or second axis of the ion guide (and/or the transition region 33), e.g. by applying different voltages to electrodes of the ion guide at different axial locations. Alternatively, or additionally, ions may be accelerated into CID fragmentation with the gas by travelling one or more DC potential barrier along the first and/or second ion guide portions 30,32 so as to urge the ions to collide with the gas molecules. This may be performed by successively applying one or more transient DC voltage to successive electrodes along the ion guide. The one or more DC potential barrier may be repeatedly travelled along the ion guide. The one or more DC potential barrier may be travelled along the ion guide in a direction from the ion entrance (cone 20) to the ion exit (differential pumping aperture 26) of the first vacuum chamber 24, or from the ion exit to the ion entrance of the first vacuum chamber 24 (i.e. opposing the gas flow to cause higher collision energies).

(23) As described above, the embodiments allow the handling of large gas loads into the instrument, enabling the use of a relatively large sampling cone 20 to capture significantly more ions from the upstream high pressure region 22. For example, the sampling cone 20 may have a diameter of about 0.8 mm. The ion transmission into the instrument and signal to noise ratio of the instrument are therefore improved. For example, the ion transmission may be increased by a factor of at least 25 and the signal to noise ratio may be increased by a factor of at least 5, as compared to arrangements having conventional multipole ion guides.

(24) The embodiments provide increased collisions of the ions with the gas molecules due to the high gas load, enabling a high sequence coverage of analytes. For example, close to 100% sequence coverage was obtained in a monoclonal antibody (mAb) tryptically digested peptide mapping LC-MS experiment.

(25) By way of example only, LC-MS and LC-MS/MS experiments for NIST mAb tryptically digested peptide mapping will now be described. NIST monoclonal antibody Reference Material 8671 (NIST mAb) was reduced and tryptically digested, lyophilized. The contents of one vial were reconstituted in water before injection. Analyses of this sample were performed using a Waters ACQUITY UPLC H-Class Bio LC system coupled to a single stage orthogonal acceleration TOF system (i.e. in which a TOF mass analyser is located in the second vacuum chamber). The separation method and the mass spectrometry conditions are outlined below.

(26) LC Conditions:

(27) Columns: ACQUITY UPLC Peptide BEH C18 Column, 300 Å, 1.7 μm, 2.1 mm×100 mm

(28) Mobile Phase A: 0.1% (w/v) Formic acid in water

(29) Mobile Phase B: 0.1% (w/v) Formic acid in acetonitrile

(30) Column Temperature: 60° C.

(31) Injection Volume: 2 μL

(32) Sample Concentration: 0.2 μg/μL

(33) Sample Diluent: water

(34) UV Detection: 214 nm (20 Hz)

(35) Gradient Table:

(36) TABLE-US-00001 Time(min) Flow Rate(mL/min) % A % B Curve Initial 0.200 99.0 1.0 Initial 1.00 0.200 99.0 1.0 6 60.00 0.200 60.0 40.0 6 61.00 0.200 25.0 75.0 6 63.00 0.200 25.0 75.0 6 64.00 0.200 99.0 1.0 6 75.00 0.200 99.0 1.0 6

(37) FIG. 3 shows the total ion current as a function of LC retention time for both a low fragmentation mode (upper plot) and a high fragmentation mode (lower plot). In the low fragmentation mode the voltage applied to the differential pumping aperture 26 was set such that the ions were not accelerated into a significant level of CID fragmentation. As such, the ion signal is primarily due to precursor ions. In the high fragmentation mode the voltage applied to the differential pumping aperture 26 was set such that the ions were accelerated through a potential difference into a significant level of CID fragmentation. As such, the ion signal contains significant contributions from fragment ions.

(38) FIG. 4 shows the 98% coverage maps of the peptide mapping experiment with the NIST mAb sample.

(39) FIG. 5 shows MS/MS fragmentations of one of the NIST mAb tryptic peptide and demonstrates the high MS/MS fragmentation quality of the system.

(40) The experiment shows that fragmentation is performed more efficiently than in arrangements having conventional multipole ion guides, and the technique therefore produces fragments that have close to 100% sequence matching coverage (e.g. for 150 KDa monoclonal antibody molecules).

(41) Although a specific example has been described above, the techniques described herein are applicable to the fragmentation of other species and forms of molecules. For example, embodiments are contemplated wherein the fragmentation and analysis of small pharmaceutical drugs, pesticides in food, environmental contaminants, or other biological molecules (such as lipids and oligonucleotides, synthetic polymers, etc.) are performed.

(42) Although the present invention has been described with reference to preferred embodiments, it will be understood by those skilled in the art that various changes in form and detail may be made without departing from the scope of the invention as set forth in the accompanying claims.

(43) For example, although the embodiments described above include an ion guide having two conjoined ion guide portions comprising ring electrodes, other embodiments are contemplated.

(44) FIG. 6 shows a cross-section through the ion guide (at the transition region 33) in an embodiment wherein the ion guide is formed from stacked plate electrodes instead of ring electrodes. Adjacent plate electrodes may be maintained at different (e.g. opposite) phases of an RF voltage. The plate electrodes which define the first axial path of the ion guide may be maintained at a first DC voltage DC1. The plate electrodes which define the second axial path of the ion guide may be maintained at a second, different voltage DC2.

(45) FIG. 7 shows a cross-section through the ion guide (at the transition region 33) in an embodiment wherein the ion guide is formed from rod sets. Adjacent rods may be maintained at different (e.g. opposite) phases of an RF voltage. The rod electrodes which define the first axial path of the ion guide may be maintained at a first DC voltage DC1. The rod electrodes which define the second axial path of the ion guide may be maintained at a second, different voltage DC2.