Intelligent target-based acquisition

Patent metadata

Field	Value
Publication number	US-10242853-B2
Application number	US-201515318254-A
Country	US
Kind code	B2
Filing date	Jun 12, 2015
Priority date	Jun 13, 2014
Publication date	Mar 26, 2019
Grant date	Mar 26, 2019

Abstract

A method of mass spectrometry comprises ionizing a sample eluting from a separation device in order to generate a plurality of parent ions. The method further comprises generating a target list of ions, which includes a predicted mass to charge ratio, a predicted chromatographic retention or elution time, and a predicted ion mobility drift time, derived from a model. Multiple cycles of operation are then performed as the sample elutes from the separation device. Each cycle of operation includes mass filtering the parent ions so that selected ions having mass to charge ratios within a first mass to charge ratio range are onwardly transmitted to a fragmentation or reaction device. The target list is then checked and the model is updated accordingly. The first mass to charge ratio range can then be adjusted in response to the updated model.

First claim

The invention claimed is:

1. A method of mass spectrometry comprising:
ionising a sample eluting from a separation device in order to generate a plurality of parent ions;
generating a target list of ions, wherein said target list comprises a predicted mass to charge ratio and at least one of: a predicted chromatographic retention or elution time; and a predicted ion mobility drift time, cross-sectional area or other data relating to ion mobility, derived from a model;
performing multiple cycles of operation as said sample elutes from said separation device, wherein each cycle of operation includes mass filtering said parent ions so that selected ions having mass to charge ratios within a first mass to charge ratio range are onwardly transmitted to a fragmentation or reaction device;
comparing or checking said target list and updating said model; and
adjusting said first mass to charge ratio range that is used to select ions for onward transmission to said fragmentation or reaction device or adjusting the width of said first mass to charge ratio range that is used to select ions for onward transmission to said fragmentation or reaction device in response to said updated model.

2. A method as claimed in claim 1 , further comprising updating said target list so as to no longer select precursor or parent ions which are associated with previously identified parent compounds or updating said target list to select precursor or parent ions which are not associated with previously identified parent compounds.

3. A method as claimed in claim 1 , further comprising processing said target list and generating an initial time line.

4. A method as claimed in claim 3 , further comprising
sorting target ions by chromatographic retention or elution time or the intensity of the A0 molecular ion of each charge group.

5. A method as claimed in claim 3 , wherein the step of generating said initial time line further comprises using peptide ionisation rank information.

6. A method as claimed in claim 3 , wherein the step of generating said initial time line further comprises prioritizing higher ionizing peptides from lower molecular weight proteins.

7. A method as claimed in claim 1 , wherein each cycle of operation includes mass filtering said parent ions based on said target list so that selected ions having mass to charge ratios within a first mass to charge ratio range are onwardly transmitted to a fragmentation or reaction device.

8. A method as claimed in claim 1 , wherein each cycle of operation further includes fragmenting or reacting said selected ions in or within said fragmentation or reaction device so as to form fragment or product ions.

9. A method as claimed in claim 1 , wherein each cycle of operation further includes obtaining parent ion or fragment or product ion mass spectral data.

10. A method as claimed in claim 1 , wherein said step of comparing or checking said target list further includes identifying parent compounds using ion mass spectral data.

11. A method as claimed in claim 1 , wherein said target list further comprises a predicted fragmentation pattern derived from a model.

12. A method as claimed in claim 1 , wherein said model includes at least one of: a mass to charge ratio model; a chromatographic retention or elution time model; an ion mobility drift time model; and a fragmentation model.

13. A method as claimed in claim 1 , wherein each cycle of operation further includes separating or selecting parent ions or fragment or product ions according to their ion mobility.

14. A method as claimed in claim 13 , further comprising adjusting a first ion mobility drift time range used to select parent ions or fragment or product ions or adjusting the width of a first ion mobility drift time range used to select parent ions or fragment or product ions in response to said updated model.

15. A method as claimed in claim 1 , wherein said model is updated based on at least one of: a derived relationship between (i) modelled chromatographic retention or elution times and (ii) operational or experimental chromatographic retention or elution times; and a derived relationship between (i) modelled ion mobility drift times and (ii) operational or experimental ion mobility drift times.

16. A method as claimed in claim 15 , wherein said derived relationship is derived using a line of best fit.

17. A mass spectrometer comprising:
an ion source arranged and adapted to ionise a sample eluting from a separation device in order to generate a plurality of parent ions; and
a control system arranged and adapted:
(i) to generate a target list of ions, wherein said target list comprises a predicted mass to charge ratio and at least one of: a predicted chromatographic retention or elution time; and a predicted ion mobility drift time, cross-sectional area or other data relating to ion mobility, derived from a model;
(ii) to perform multiple cycles of operation as said sample elutes from said separation device, wherein each cycle of operation includes mass filtering said parent ions so that selected ions having mass to charge ratios within a first mass to charge ratio range are onwardly transmitted to a fragmentation or reaction device;
(iii) to compare or check said target list and update said model; and
(iv) to adjust said first mass to charge ratio range that is used to select ions for onward transmission to said fragmentation or reaction device or to adjust the width of said first mass to charge ratio range that is used to select ions for onward transmission to said fragmentation or reaction device in response to said updated model.

Assignees

• Waters Technologies Corp

Inventors

• Geromanos Scott J
• Ciavarini Steven J
• Chen Weibin
• Houel Stephane

Classifications

• H01J49/0036 Primary

  Step by step routines describing the handling of the data generated during a measurement · CPC title

• G01N30/8675

  Evaluation, i.e. decoding of the signal into analytical information (for analysis of specific compounds see also G01N30/88 and subgroups of G01N33/00; chemical libraries per se C40B) · CPC title

• H01J49/0031

  Step by step routines describing the use of the apparatus (H01J49/0081 takes precedence) · CPC title

• G01N30/8679 Primary

  Target compound analysis, i.e. whereby a limited number of peaks is analysed · CPC title

• G01N30/8693

  Models, e.g. prediction of retention times, method development and validation · CPC title