GB2451963A

GB2451963A - A method of mass spectrometry suitable for the identification of peptide ions

Info

Publication number: GB2451963A
Application number: GB0816196A
Authority: GB
Inventors: Robert Harold Bateman
Original assignee: Micromass UK Ltd
Current assignee: Micromass UK Ltd
Priority date: 2005-11-23
Filing date: 2006-11-23
Publication date: 2009-02-18
Anticipated expiration: 2026-11-23
Also published as: GB0523811D0; GB0623377D0; GB2443570A; GB0816196D0; GB2435714B; CA2628927C; GB2451963B; GB2435714A; WO2007060437A2; WO2007060437A3; JP4959713B2; CA2628927A1; EP1952425A2; JP2009516843A; CA2835042A1; GB2443570B; GB0801092D0

Abstract

A method of mass spectrometry is disclosed wherein a Surface Induced Dissociation (SID) fragmentation device is repeatedly switched between a high fragmentation mode and a low fragmentation mode. Parent ions from a first sample are passed through the device and parent ion mass spectra and fragmentation ion mass spectra are obtained. Parent ions from a second sample are then passed through the device and a second set of parent ion mass spectra and fragmentation ion mass spectra are obtained. The mass spectra are then compared and if either certain parent ions or certain fragmentation ions in the two samples are expressed differently then further analysis is performed to seek to identify the ions which are expressed differently in the two different samples.

Description

INTELLECTUAL

.. PROPERTY OFFICE Application No. GBOS 16196.0 RTM Date:12 December 2008 The following terms are registered trademarks and should be read as such wherever they occur in this document: Orbitrap Intellectual Properly Office is an operating name of the Patent Office wWW.ipo gov.uk

A METHOD OF MASS SPECTROMETRY SUITABLE FOR IDENTIFICATION OF PEPTIDE

IONS

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The present invention relates to a method of mass spectrometry and a mass spectrometer.

It has become common practice to analyse proteins by first enzymatically or chemically digesting the protein and then analysing the peptide products by mass spectrometry. The mass spectrometry analysis of the peptide products normally entails measuring the mass of the peptide products. This method is sometimes referred to as.

"peptide mapping" or "peptide fingerprinting".

It is also known to induce parent or precursor peptide ions to fragment and to then measure the mass of one or more fragment or daughter ions as a way of seeking to identify the parent or precursor peptide ion. The fragmentation pattern of a peptide ion has also been shown to be a successful way of distinguishing isobaric peptide ions. Thus the mass to charge ratio of one or more fragment or daughter ions may be used to identify the parent or precursor peptide ion and hence the protein from which the peptide was derived. In some instances the partial sequence of the peptide can also be determined from the fragment or daughter ion spectrum. This information may be used to determine candidate proteins by searching protein and genomic databases.

Alternatively, a candidate protein may be eliminated or confirmed by comparing the masses of one or more observed fragment or daughter ions with the masses of fragment or daughter ions which might be expected to be observed based upon the peptide sequence of the candidate protein in question. The confidence in the identification increases as more peptide parent or precursor ions are induced to fragment and their fragment masses are shown to match those expected.

It is desired to provide an improved method of mass spectrometry and an improved mass spectrometer.

According to an aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising an Electron Capture Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Capture Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon interacting with electrons to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising an Electron Capture Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Capture Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon interacting with electrons to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; and comparing the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to the preferred embodiment the parent or precursor ions comprise doubly, triply, quadruply charged ions or ions having five or more charges.

According to the preferred embodiment the Electron Capture Dissociation fragmentation device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

In the first mode of operation the electrons preferably have an energy selected from the group consisting of: Ci) < 1 eV; (ii) 1-2 eV; (iii) 2-3 eV; (iv)3-4 eV; and Cv) 4-5 eV. In the first mode of operation the relatively low energy electrons are preferably confined by a relatively strong magnetic field. The ions to be fragmented are preferably confined within an ion guide. An AC or RF voltage is preferably app.Lied to the electrodes of the ion guide in order to create a radial pseudo-potential field or well which preferably acts to confine ions radially within the ion guide.

The relatively low energy electrons are preferably confined by a magnetic field which preferably overlaps or superimposes the ion guiding region of the ion guide so that multiply charged analyte ions are caused to interact with the relatively low energy electrons.

Fragmentation of ions by Electron Capture Dissociation preferably does not involve causing internal vibrational energy to be introduced to the ions.

The method preferably further comprises providing an electron source. In the first mode of operation the electron source preferably generates a plurality of electrons which are arranged to interact with the parent or precursor ions. In the second mode of operation the electron source is preferably switched OFF so that analyte ions preferably do not interact with any electrons and hence preferably are not caused to fragment.

According to an aspect of the present invention there is provided method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising an Electron Transfer Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Transfer Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon interacting with reagent ions to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising an Electron Transfer Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Transfer Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon interacting with reagent ions to Produce-fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; and comparing the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to the preferred embodiment the Electron Transfer Dissociation fragmentation device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

According to an aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying the Surface Induced Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying the Surface Induced Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; and comparing the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to the preferred embodiment the Surface Induced Dissociation fragmentation device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

In the first mode of operation the parent or precursor ions are preferably directed, diverted or deflected on to the surface or target plate. In the second mode of operation the parent or precursor ions are preferably not directed, diverted or deflected on to the surface or target plate.

The surface or target plate preferably comprises a self-assembled monolayer. The surface or target plate preferably comprises a fluorocarbon or hydrocarbon monolayer.

The surface or target plane is preferably arranged in a plane which is substantially parallel to the direction of travel of the parent or precursor ions in the second mode of operation i.e. when ions are preferably transmitted past the surface or target plate without being directed on to the surface or target plate.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first parent or precursor ions from the first sample which have a first: mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sainple which have the same first mass to charge ratio; and comparing the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; wherein the collision, fragmentation or reaction device selected from the group consisting of: (i) an Electron Collision or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation (PID') fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmentation device; (vii) an in-source fragmentation device; (viii) an ion-source Collision Induced Dissociation fragmentation device; (ix) a thermal or temperature source fragmentation device; (x) an electric field induced fragmentation device; (xi) a magnetic field induced fragmentation device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion-ion reaction fragmentation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastable ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an ion-metastable atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product iOns; (xxii) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxiv) an ion- metastable atom reaction device for reacting ions to form adduct or product ions.

According to the preferred embodiment the parent or precursor ions comprise doubly, triply, quadrup].y charged ions or ions having five or more charges.

According to the preferred embodiment the collision, fragmentation or reaction device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising: pass ing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising an Electron Capture Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Capture Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon interacting with electrons to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising an Electron Capture Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Capture Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon interacting with electrons to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; determining a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; determining a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sainpie; and -comparing the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

In the first mode of operation the electrons preferably have an energy selected from the group consisting of: (i) < 1 eV; (ii) 1-2 eV; (iii) 2-3 eV; (iv') 3-4 eV; and (v) 4-5 eV.

In the first mode of operation the electrons are preferably

confined by a magnetic field.

The method preferably further comprises providing an electron source.

In the first mode of operation the electron source preferably generates a plurality of electrons which are arranged to interact with the parent or precursor ions. In the second mode of operation the electron source is preferably switched OFF.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising:

-

passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising an Electron Transfer Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Transfer Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon interacting with reagent ions to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a secondsamp1e to a Collision, fragmentation or reaction device comprising an Electron Transfer Dissociation fragmentation device; repeatedly switching, altering or varying the Electron Transfer Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon interacting with reagent ions to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; determining a first ratio of the intensity of the first parene or precursor ions to the intensity of other parent or precursor ions in the first sample; determining a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; and comparing the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

-11 -According to the preferred embodiment the parent or precursor ions comprise doubly, triply, quadruply charged ions or ions having five or more charges.

According to another aspect of the present invention there is provided ainethod of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaccion device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying the Surface Induced Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying the Surface Induced Dissociation fragmentation device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; - 12 -determining a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; determining a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; and comparing the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to the preferred embodiment the Suf ace Induced Dissociation fragmentation device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

The surface or target plane is preferably arranged in a plane which is substantially parallel to the direction of travel of the parent or precursor ions in the second mode of operation.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first parent or precursor ions from the first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from the second sample which have the same first mass to charge ratio; determining a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; determining a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; and comparing the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; wherein the collision, fragmentation or reaction device selected from the group consisting of: (i) an Electron Collision or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation ("PID") fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced -14 -dissociation device; (vi) nozzle-skjer interface fragmentation device; (vii) an in-source fragmentation device; (viii) an ion-source Collision Induced Dissociation fragmentation device; (ix) a thermal or temperature source fragmentation device; (x) an electric field induced fragmentation device; (xi) a magnetic field induced fragmentation device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion-ion reaction fragmentation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastab].e ion reaction fragmentation -device; (xvii) an ion-nietastable molecule reaction fragmentation device; (xviii) an ion-metastable atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxii) an lon-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction device for reacting loris to form adduct or product Ions; and (xxiv) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.

According to the preferred embodiment the parent or precursor ions comprise doubly, triply, quadruply charged ions or ions having five or more charges.' According to the preferred embodiment the collision, fragmentation or reaction device is preferably repeatedly switched between the first and second modes during a single experimental run or during a single analysis of a sample.

A reaction device should be understood as comprising a device wherein ions, atoms or molecules are rearranged or reacted so as to form a new species of ion, atom or molecule. An X-Y reaction fragmentation device should be understood as meaning a device wherein X and Y combine to form a product which then fragments. This is different to a fragmentation device per se wherein ions ma y be caused to fragment without first forming a product. An X-Y reaction device should be understood as meaning a device wherein X and Y combine to -15 -form a product and wherein the product does not necessarily then fragment.

According to the present invention ions are collided, fragmented or reacted in a device other than a Collision Induced Dissociation fragmentation device. According to a particularly preferred embodiment an Electron Capture Dissociation (ECD") or an Electron Transfer Dissociation ("ETD") fragmentation device are used to fragment analyte ions.

Polypeptjde chains are made up of amino acid residues which -have certain masses. There are three different bonds along a peptide-- backbone and when a bond is broken the charge may remain either at -the N-terminal part of the structure or the C-terminal part of the structure. When a polypeptide is fragmented there are six possible fragmentation series which are cornnionly referred to as: a, b, c and x, y, z. With Collision Induced Dissociation the most common fragmentation route is for fragmentation to occur through the amide bond (II). If the charge remains on the N-terminal then the ion is referred to as a b series ion. If the charge remains on the C-terminal then the ion is referred to as a y series ion.

Subscripts may be used to indicate how many amino acids residues are contained in the fragment. For example, b3 is the fragment ion resulting from cleavage of the amide bond (II) such that charge remains on the N-terminal and wherein there are 3 amino acid residues in the fragment.

According to an embodiment of the present invention when an Electron Capture Dissociation (ECD#) or an Electron Transfer Dissociation ("ETD") fragmentation device is used to fragment ions.

then the pOlypeptide chain can be fragmented at different positions to those positions where fragmentation would be expected to occur if the polypeptide were fragmented by Collision Induced Dissociation.

In particular, an Electron Capture Dissociation (ECD) or an Electron Transfer Dissociation (ETDN) device enable x and c series fragment OflS predominantly to be produced. In certain circumstances it is particularly advantageous to cause ions to fragment into x and -16 -c series fragment ions rather than b and y series fragment ions (as would be the case by Collision Induced Dissociation). In some situations a more complete sequence is possible using ECD or ETD and there can also be less ambiguity in identifying fragment ions. This can make the process of sequencing the peptide easier.

Polypeptides may also be modified by Post Translational Modifications such as phosphorylation. The use of an ECD or ETD fragmentation device and the resulting fragmentation series which are produced enables Post Translational Modifications such as phosphorylation to be more easily observed. --It is also possible to make a determination as to where the modification occurs along the length of the polypeptide.

According to another embodiment the collision, fragmentation or reaction device may comprise a Surface Induced Dissociation fragmentation device. Collision Induced Dissociation can be viewed as being a relatively slow process in that fragmentation is often the result of multiple collisions between ions and gas molecules. As a result fragmentation tends to be averaged out and a relatively broad range of fragmentation products are typically observed. In contrast, Surface Induced Dissociation can be viewed s being a relatively sudden or instantaneots process. As a result a polypeptide may fragment in a very specific manner. In certain situations this can be particularly useful since it can reveal certain useful information about the structure of the polypeptide.

It will therefore be appreciated that the present invention is particularly advantageous in that parent or precursor ions are preferably fragmented via different fragmentation routes to those that may be obtained by Collision Induced Dissociation. Furthermore, the present invention also enables Post Translational Modifications of peptides to be observed and a determination to be made as to where the modification sits in the peptide. The present invention is also particularly advantageous compared to conventional approaches to fragmenting analyte ions and attempting to elucidate structural information relating to the analyte ions by analysing the corresponding fragment ions.

-17 -The present invention is therefore particularly advantageous compared to conventional arrangements.

According to the preferred embodiment the method preferably further comprises automatically switching, altering or varying the cOllision, fragmentation or reaction device between at least the first mode and the second mode at least once every 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 seconds.

Other arrangements are also contemplated wherein instead of determining a first r.tio of first parent or precursor ions to other parent or precursor ions, a first ratio of first parent or precursor ions to certain fragment,. product, daughter or adduct ions may be determined. Similarly, a second ratio of second parent or precursor ions to certain fragment, product, daughter or adduct ions may be determined and the first and second ratios compared.

The other parent or precursor ions present in the first sample and/or the other parent or precursor ions present in the second sample may either be endogenous or exogenous to the sample. The other parent or precursor ions present in the first sample and/or the other parent or precursor ions present in the second sample may additionally be used as a chromatographic retention time standard.

According to one embodiment parent or precursor ions, preferably peptide ions, from two different samples are analysed in separate experimental runs. In each experiinental run parent or precursor ions are passed to a collision, fragmentation or reaction device. The collision, fragmentation or reaction device is preferably repeatedly switched between a fragmentation or reaction mode and a substantially non-fragmentation or reaction mode. The ions emerging from the collision, fragmentation or reaction device or which have been transmitted through the collision, fragmentation or reaction device are then preferably mass analysed. The intensity of parent or precursor ions having a certain mass to charge ratio in one sample are then compared with the intensity of parent or precursor ions having the same certain mass to charge ratio in the other sample. A direct comparison of the parent or precursor ion -18 - expression level may be made or the intensity of parent or precursor ions in a sample may first be compared with an internal standard. n indirect comparison may therefore be made between the ratio of parent: or precursor ions in one sample relative to the intensity of parent or precursor ions relating to an internal standard and the ratio of parent or precursor ions in the other sample relative to the intensity of parent or precursor ions relating to preferably the same internal standard. A comparison of the two ratios may then be made.

Although the preferred embodiment is described as relating to comparing the parent or precursor ion expression level in two samples, it is apparent that the expression level of parent or -precursor ions in three or more samples may be compared.

Parent or precursor ions may be considered to be expressed s.gnificantly differently in two samples if their expression level differs by more than 1%, 10%, 50%, 100%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 1000%, 5000% or 10000%.

The collision, fragmentation or reaction device is preferably maintained at a pressure selected from the group consisting of: (i) greater than or equal to 0.0001 mbar; (ii) greater than or equal to 0.001 mbar; (iii) greater than or equal to 0.005 mbar; (iv) greater than or equal to 0.01 mbar; (v) between 0.0001 and 100 mbar; and (vi) between 0.001 and 10 nthar. Preferably, the collision, -fragmentation or reaction device is maintained at a pressure selected from the group consisting of: (i) greater than or equal to 0.0001 mbar; (ii) greater than or equal to 0.0005 mbar; (iii) greater than or equal to 0.001 mbar; (iv) greater than or equal to 0.005 mbar; Cv) greater than or equal to 0.01 mbar; (vi) greater than or equal to 0.05 mbar; (vii) greater than or equal to 0.1 mbar; (viii) greater than or equal to 0.5 rnbar; (ix) greater than or equal to 1 mbar; (x) greater than or equal to 5 mbar; and (xi) greater than or equal to 10 mbar.

Preferably, the collision, fragmentation or reaction device is maintained at a pressure selected from the group consisting of: Ci.) less than or equal to 10 mbar; (ii) less than or equal to S mbar; (iii) less than or equal. to 1 mbar; (iv) less than or equal to 0.5 ntbar; (v) less than or equal to 0.1 mbar; (vi) less than or equal to -19 - 0.05 mbar; (vii) less than or equal to 0.01 inbar; (viii) less than or equal to 0. 005 uthar; (ix) less than or equal to 0.00? nthar; (x) less than or equal to 0.0005 inbar; and (xi) less than or equal to 0.0001 mbar.

According to a less preferred embodiment, gas in the collision, fragmentation or reaction device may be maintained at a first pressure when the collision, fragmentation or reaction device is in the high fragmentation or reaction mode and at a second lower pressure when the collision, fragmentation or reaction device is in the low fragmentation or reaction mode. According to another less preferred embodiment, gas in the collision, fragmentation or reaction device may comprise a first gas or a first mixture of gases when the collision, fragmentation or reaction device is in the high fragmentation or reaction mode and a second different gas or a second different mixture of gases when the collision, fragmentation or reaction device is in the low fragmentation or reaction mode.

Parent or precursor ions which are considered to be parent or precursor ions of interest are preferably identified. This may comprise determining the mass to charge ratio of the parent or precursor ions of interest, preferably accurately to less than or equal to 20 ppm, 15 ppm, 10 ppm or 5 ppm. The determined mass to charge ratio of the parent or precursor ions of interest may then be compared with a database of ions and their corresponding mass to charge ratios and hence the identity of the parent or predursor ions of interest can be established.

According to the preferred embodiment the step of identifying the parent or precursor ions of interest comprises identifying one or more fragment, product, daughter or adduct ions which are determined to result from fragmentation of the parent or precursor ions of interest. Preferably, the step of identifying one or more fragment, product, daughter or adduct ions further comprises determining the mass to charge ratio of the one or more fragment, product, daughter or adduct ions to less than or equal to 20 ppm, 15 ppm, 10 ppm or 5 ppm.

-20 -The step of identifying first parent or precursor ions of interest may comprise determining whether parent or precursor ions are observed in a mass spectrum obtained when the collision, fragmentation or reaction device is in the low fragmentation or S reaction mode for a certain time period and the first fragment, product, daughter or adduct ions are observed in a mass spectrum obtained either immediately before the certain time period, when the collision, fragmentation or reaction device is in the high fragmentation or reaction mode, or immediately after the certain time period, when the-collision, fragmentation or reaction device is in the high fragmentation or reaction mode.

The step of identifying first parent or precursor ions of interest may comprise comparing the elution times of parent or precursor ions with the pseudo-elution time of first fragment, product, daughter or adduct ions. The fragment, product, daughter or adduct ions are referred to as having a pseudo-elution time since fragment, product, daughter or adduct ions do not actually physically elute from a chromatography column. However, since at least some of the fragment, product, daughter or adduct ions are fairly unique to particular parent or precursor ions, and the parent or precursor ions may elute from the chromatography column only at particular times, then the corresponding fragment, product, daughter or adduct ions may similarly only be observed at substantially the same elution time as their related parent or precursor ions. Similarly, the step of identifying first parent or precursor ions of interest may comprise comparing the elution profiles of parent or precursor loris with the pseudo-eluti.on profile of first fragment, product, daughter or adduct ions. Again, although fragment, product, daughter or adduct ions do not actually physically elute from a chromatography column, they can be considered to have an effective elution profile since they will tend to be observed only when specific parent or precursor ions elute from the column and as the intensity of the eluting parent or precursor ions varies over a few seconds so similarly the intensity of characteristic fragment, product, daughter or adduct ions will also vary in a similar manner.

-21 -Ions may be determined to be parent or precursor ions by comparing two mass spectra obtained one after the other, a first mass spectrum being obtained when the collision, fragmentation or reaction device was in a high fragmentation or reaction mode and a second mass spectrum obtained when the collision, fragmentation or reaction device was in a low fragmentation or reaction mode, wherein ions are determined to be parent or precursor ions if a peak corresponding to the ions in the second mass spectrum is more intense than a peak corresponding to the ions in the first mass spectrum. Similarly, ions may be determined to be fragment, product, daughter or adduct ions if a peak corresponding to the ions in the first mass spectrum is more intense than a peak corresponding to the ions in the second mass spectrum. According to another embodiment, a mass filter may be provided upstream of the collision, fragmentation or reaction device wherein the mass filter is arranged to transmit ions having mass to charge ratios within a first range but to substantially attenuate ions having mass to charge ratios within a second range and wherein ions are determined to be fraqinent, product, daughter or adduct ions if they are determined to have a mass to charge ratio falling within the second range.

The first parent or precursor ions and the second parent or precursor ions are preferably determined to have mass to charge ratios which-differ by less than or equal to 40 ppm, 35 ppm, 30 ppm, ppm, 20 ppm, 15 ppm, 10 ppm or 5 ppm. The first parent or precursor ions and the second parent or precursor ions may have been determined to have eluted from a chromatography column after substantially the same elution time. The first parent or precursor ions may also have been determined to have given rise to one or more first fragment, product, daughter or adduct ions and the second parent or precursor ions may have been determined to have given rise to one or more second fragment, product, daughter or adduct ions, wherein the one or more first fragment, product, daughter or adduct ions and the one or more second fragment, product, daughter or adduct ions have substantially the same mass to charge ratio. The mass to charge ratio of the one or more first fragment, product, daughter or adduct ions and the one or more second fragment, product, daughter or adduct ions may be determined to differ by less than or equal to 40 ppm, 35 ppm, 30 ppm, 25 ppm, 20 ppm, 15 ppm, 10 ppm or 5 ppm.

The first parent or precursor ions may also be determined to have given rise to one or more first fragment, product, daughter or adduct ions and the second parent or precursor ions may have been determined to have given rise to one or more second fragment, product, daughter or adduct ions and wherein the first parent or precursor ions and the second parent or precursor ions are observed in mass spectra relating to data obtained in the low fragmentation or reaction mode at a certain point in time and the one or more first and second fragment, product, daughter or adduct ions are observed in mass spectra relating to data obtained either immediately before the certain point in time, when the collision, fragmentation or reaction device is in the high fragmentation or reaction mode, or immediately after the certain point in time, when the collision, fragmentation or reaction device is in the high fragmentation or reaction mode.

The first parent or precursor ions may be determined to have given rise to one or more first fragment, product, daughter or adduct ions and the second parent or precursor ions may be determined to have given rise to one or more second fragment, product, daughter or adduct ions if the first fragment, product, daughter or adduct ions have substantially the same pseudo-elution time as the second fragment, product, daughter or adduct ions.

The first parent or precursor ions may be determined to have given rise to one or more first fragment, product, daughter or adduct ions and the second parent or precursor ions may be determined to have given rise to one or more second fragment, product, daughter or adduct ions and wherein the first parent or precursor ions are determined to have an elution profile which correlates with a pseudo-elution profile of a first fragment, product, daughter or adduct ion and wherein the corresponding second parent or precursor ions are determined to have an elution profile which correlates with a pseudo-elution profile of a second fragment, product, daughter or adduct ion.

-23 -According to another embodiment the first parent or precursor ions and the second parent or precursor ions which are being compared may be determjnedto be multiply charged. This may rule out a number of fragment, product, daughter or adduct ions which quite often tend to be singly charged. The first parent or precursor ions and the second parent or precursor ions may according to a more preferred embodiment be determined to have the same charge state. According to another embodiment, the parent or precursor ions being compared in the two different samples may be determined to give rise to fragment, product, daughter or adduct ions which have the same charge state.

The first sample and/or the second sample may comprise a plurality of different biopolymers, proteins, peptides, polypeptides, oligionucleotides, oligionucleosides, amino acids, carbohydrates, sugars, lipids, fatty acids, vitamins, hormones, portions or fragments of DNA, portions or fragments of cDNA, portions or fragments of RNA, portions or fragments of mRNA, portions or fragments of tRNA, polyc].onal antibodies, monoclonal antibodies, ribonucleases, enzymes, metabolites, polysaccharides, phosphorylated peptides, phosphorylated proteins, glycopeptides, glycoproteins or steroids. The first sample and/or the second sample may also comprise at least 2, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, or 5000 molecules having different identities.

The first sample may be taken from a diseased organism and the second sample may be taken from a non-diseased organism.

Alternatively, the first sample may be taken from a treated organism and the second sample may be taken from a non-treated organism.

According to another embodiment the first sample may be taken from a mutant organism and the second sample may be taken from a wild type organism.

Molecules from the first and/or second samples are preferably separated from a mixture of other molecules prior to being ionised by High Performance Liquid Chromatography (HPLC), anion exchange, anion exchange chromatography, cation exchange, cation exchange chromatography, ion pair reversed-phase chromatography, -24 -chromatography, single dimensional electrophoresis, multi-dimensional e].ectrophoresjs, size exclusion, affinity, reverse phase chromatography, Capillary Elec trophoresis Chromatography (CEC U), electrophoresjs, ion mobility separation, Field Asymmetric Ion Mobility Separation (FAIMS) or capillary electrophoresis.

According to a particularly preferred embodiment the first and second sample ions may comprise peptide ions. The peptide ions preferably comprise the digest products of one or more proteins. n attempt may be made to identify a protein which correlates with parent peptide ions of interest. Preferably, a determination-is made as to which peptide products are predicted to be formed when a protein is digested and it is then determined whether any predicted peptide product(s) correlate with parent or precursor ions of interest. A determination may also be made as to whether the parent or precursor ions of interest correlate with one or more proteins.

The first and second samples may be taken from the same organism or from different organisms.

A check may be made to confirm that the first and second parent or precursor ions being compared really are parent or precursor ions rather than fragment, product, daughter or adduct ions. A high fragmentation mass spectrum relating to data obtained in the high fragmentation or reaction mode may be compared with a low fragmentation mass spectrum relating to data obtained in the low fragmentation or reaction mode wherein the mass spectra were obtained at substantially the same time. A determination may be made that the first and/or the second parent or precursor ions are not fragment, product, daughter or adduct ions if the first and/or the second parent or precursor ions have a greater intensity in the low fragmentation mass spectrum relative to the high fragmentation mass spectrwn. Similarly, fragment, product, daughter or aciduct ions may be recognised by noting ions having a greater intensity in the high fragmentation mass spectrum relative to the low fragmentation mass spectrum.

Parent or precursor ions from the first sample and parent or precursor ions from the second sample are preferably passed to the -25 -same collision, fragmentation or reaction device. However, according to a less preferred embodiment, parent or precursor ions from the first sample and parent or precursor ions from the second sample may be passed to different collision, fragmentation or reaction devices.

According to another aspect of the present invention there is provided a mass spectrometer comprising: an Electron Capture Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon interactinq with electrons to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; and (iii) compares the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to another aspect of the present invention there is provided a mass spectrometer comprising: an Electron Transfer Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon interacting with negatively charged reagent ions to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and -26 -a control system which in use: (1) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; and (iii) compares the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to another aspect of the present invention there is provided a mass spectrometer comprising: a Surface Induced Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon impinging upon a surface or target plate to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; and (iii) compares the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

-27 -According to an aspect of the present invention there is provided a mass spectrometer comprising: a collision, fragmentation or reaction device which isarranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in USC: - (1) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; and (iii) compares the intensity of the first parent or precursor ions with the intensity of the second parent or precursor ions; wherein if the intensity of the first parent or precursor ions differs from the intensity of the second parent or precursor ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; wherein the collision, fragmentation or reaction device selected from the group consisting of: (1) an Electron Collision or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation (PIDu) fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmentation device; (vii) an in-source fragmentation device; (viii) an ion-source Collision Induced Dissociation fragmentation device; (ix) a thermal or temperature source fragmentation device; Cx) an electric field induced fragmentation device; (xi) a magnetic field induced fragmentation device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion-ion reaction fragme ntation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastable ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an ion-inetastable atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxii) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxiv) an ion- metastable atom reaction device for reacting ions to form adduct or product ions.

According to another aspect of the present invention there is provided a mass spectrometer comprising: an Electron Capture Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon interacting with electrons to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; (iii) determines a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; (iv) determines a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; -29 - (v) compares the first parent ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount thri either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to an aspect of the present invention there is provided a mass spectrometer comprising: an Electron Transfer Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor -ions are fragmented upon interacting with negatively charged reagent ions to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: Ci) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor loris from a second sample which have the same first mass to charge ratio; (iii) determines a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; (iv) determines a sécond ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; Cv) compares the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to an aspect of the present invention there is provided a mass spectrometer comprising: a Surface Induced Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in -30 -use between a first mode wherein at least some parent or precursor ions are fragmented upon impinging upon a surface or target plate to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; (iii) determines a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; (iv) determines a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sample; (v) compares the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest.

According to an aspect of the present invention there is provided a mass spectrometer comprising: a collision, fragmentation or reaction device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in use: (1) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; -31 (ii) determines the intensity of second parent or precursor ions from a second sample which have the same first mass to charge ratio; (iii) determines a first ratio of the intensity of the first parent or precursor ions to the intensity of other parent or precursor ions in the first sample; (iv) determines a second ratio of the intensity of the second parent or precursor ions to the intensity of other parent or precursor ions in the second sainp1e Cv) compares the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; wherein the collision, fragmentation or reaction device selected from the group consisting of; (i) an Electron Collisior or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation ("PID") fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; Cv) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmentation device; (vii) an in-source fragmentation device; (viii) an ion-source Collision Induced Dissociation fragmentation device; (ix) a thermal or temperature source fragmentation device; Cx) an electric field induced fragmentation device; (xi) e magnetic field induced fragmentation device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion--ion reaction fragmentation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastab].e ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an ion-rnetastable atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or -32 -product iOnS; (xxii) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxiv) an ion-roetastable atom reaction device for reacting ions to form adduct or product ions.

The mass spectrometer preferably further comprises an ion source. The ion source is preferably selected from the group consisting of: (i) an Electrospray lonisation (EsI) ion source; (ii) an Atmospheric Pressure Photo Ionisatjon ("APPI) ion Source; (iii)-an Atmospheric Pressure Chemical Ionisatjon ("APCI) ion source; (iv) a Matrix Assisted Laser Desorptjon Ionisatjon ("MALDI) ion source; (v) a Laser Desorpti.on lonisation ("LDI) ion source; (vi) an Atmospheric Pressure Ionisatjon (API") ion source; (vii) a Desorption lonisation on Silicon (DI0S") ion source; (viii) an Electron Impact (EI") ion source; (ix) a Chemical Ionisatjon ("CI") ion source; lx) a Field lonisation (FI) ion source; (xi) a Field Desorption ("FD) ion source; (xii) an Inductively Coupled Plasma ("ICP") ion source; (xiii) a Fast Atom Bombardment (TAB") ion source; lxiv) a Liquid Secondary Ion Mass Spectrometry ("LSIMS") ion source; (xv) a Desorptjon Electrospray lonisation ("DESI") ion source; (xvi) a Nickel-63 radioactive ion source; (xvii) an Atmospheric Pressure Matrix Assisted Laser Desorption lonisation ion source; and (xviii) a Thermospray ion source.

The ion source may comprise a pulsed or a continuous ion source.

According to a particularly preferred embodiment the mass spectrometer may comprise an Electrospray, Atmospheric Pressure Chemical Ionisatjon ("APCI"), Atmospheric Pressure Photo lonisation ("APPI"), Matrix Assisted Laser Desorptjon lonisation ("MALDI"), Laser Desorptjon Ionisatjon ("LDI'), Inductively Coupled Plasma ("ICP"), Fast Atom Bombardment ("FAB) or Liquid Secondary Ions Mass Spectrometry ("LSIMS") ion source. Such ion Sources may be provided with an eluent over a period of time, the eluent having been separated from a mixture by means of liquid chromatography or capillary electrophoresis.

-33 -Alternatively, the mass spectrometer may comprise an Electron Impact (E1"), Chemical Ionisatjon (Cl1) or Field lonisation (IFIN) ion source. Such ion sources may be provided with an. eluent over a period of time, the eluent having been separated from a mixture by means of gas chromatography.

The mass analyser preferably comprises a quadrupole mass filter, a Time of Flight (TOF) mass analyser (an orthogonal acceleration Time of Flight mass analyser is particularly preferred), a 2D (linear) or 3D (doughnut shaped electrode with two endcap electrodes) ion trap, a magnetic sector analyser or--a Fourier Transform Ion Cyclotron Resonance (FTICR") mass analyser.

According to an embodiment the mass analyser is preferably selected from the group consisting of: (i) a quadrupole mass analyser; (ii) a 2D or linear quadrupole mass analyser; (iii) a Paul or 3D quadrupole mass analyser; (iv) a Penning trap mass analyser; Cv) an ion trap mass analyser; (vi) a magnetic sector mass analyser; (vii) Ion Cyclotron Resonance (ICR") mass analyser; (viii) a Fourier Transform Ion Cyclotron Resonance VFTICR") mass analyser; (ix) an electrostatic or orbitrap mass analyser; Cx) a Fourier Transform electrostatic or orbitrap mass analyser; and (xi) a Fourier Transform mass analyser; (xii) a Time of Flight mass analyser; (xiii) an orthogonal acceleration Time of Flight mass analyser; (xiv) an axial acceleration Time of Flight mass analyser; and (xv) a quadruole rod set mass filter or mass analyser.

The mass spectrometer preferably further comprises an ion trap or ion guide arranged upstream and/or downstream of the collision, fragmentation or reaction device.

The ion trap or ion guide is preferably selected from the group Consisting of: (i) a multipole rod set or a segmented multipole rod set ion trap or ion guide comprising a quadrupole rod set, a bexapole rod set, an octapole rod set or a rod set comprising more than eight rods; (ii) an ion tunnel or ion funnel ion trap or ion guide comprising a plurality of electrodes or at least 2, 5, 10, 20. 30, -34 - 40, 50, 60, 70, 80, 90 or 100 electrodes having apertures through which ions are transmitted in use, wherein at least 5%, 10%, 15%, 20%, 25%. 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the electrodes have apertures which are of substantially the same size or area or which have apertures which become progressively larger and/or smaller in size or in area; (iii) a stack or array of planar, plate or mesh electrodes, wherein the stack or array of planar, plate or mesh electrodes comprises a plurality or at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19-or 20 planar, plate or mesh electrodes and wherein at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the planar, plate or mesh electrodes are arranged generally in the plane in which ions travel in use; and (iv) an ion trap or ion guide comprising a plurality of groups of electrodes arranged axially along the length of the ion trap or ion guide, wherein each group of electrodes comprises: (a) a first and a second electrode and means for applying a DC voltage or potential to the first and second electrodes in order to confine ions in a first radial direction within the ion guide; and (b) a third and a fourth electrode and means for applying an AC or RF voltage to the third and fourth electrodes in order to confine ions in a second radial direction within the ion guide.

The ion trap or ion guide preferably comprises an ion tunnel or ion funnel ion trap or ion guide wherein at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the electrodes have internal diameters or dimensions selected from the group consisting of: (i) �= 1.0 nun; (ii) �= 2.0 nun; (iii) �= 3.0 mm; (iv) �= 4.0 nun; (v) �= 5.0 mm; (vi) �= 6.0 mm; (vii) �= 7.0 nun; (viii) �= 8.0 mm; (ix) �= 9.0 mm; (x) �= 10.0 mm; and (xi) > 10.0 nun.

The ion trap or ion guide preferably further comprises first AC or RF voltage means arranged and adapted to apply an AC or RF voltage to at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the plurality of -35 -electrodes of the ion trap or ion guide in order to confine ions radially within the ion trap or ion guide.

The first AC or RF voltage means is preferably arranged and adapted to apply an AC or RF voltage having an amplitude selected from the group consisting of: (i) < 50 V peak to peak; (ii) 50-100 V peak to peak; (iii) 100-150 V peak to peak; (iv) 150-200 V peak to peak; (v) 200-250 V peak to peak; (vi) 250-300 V peak to peak; (vii) 300-350 V peak to peak; (viii) 350-4 00 V peak to peak; (ix) 400-450 V peak to peak; (x) 450-500 V peak to peak; and (xi) > 500 V peak to peak.

The first AC or RF voltage means is preferably arranged and adapted to apply an AC or RF voltage having a frequency selected from the group consisting of: (1) < 100 kHz; (ii) 100-200 kHz; (iii) 200- 300 kllz; (iv) 300-400 kHz; (v) 400-500 kHz; (vi) 0.5-1.0 MHz; (vii) 1.0-1.5 MHz; (viii) 1.5-2.0 MHz; (ix) 2.0-2.5 MHz; (x) 2.5-3.0 MHz; (xi) 3.0-3.5 MHZ; (xii) 3.5-4.0 MHz; (xiii) 4.0-4.5 MHz; (xiv) 4.5- 5.0 MHz; (xv) 5.0-5.5 MHz; (xvi) 5.5-6.0 MHz; (xvii) 6.0-6.5 MHz; (xviii) 6.5-7.0 MHz; (xix) 7.0-7.5 MHz; (xx) 7.5-8.0 MHz; (xxi) 8.0- 8.5 MHz; (xxii) 8.5-9.0 MHz; (xxiii) 9.0-9.5 MHz; (xxiv) 9.5-10.0 MHz; and (xxv) > 10.0 MHz.

The ion trap or ion guide is preferably arranged and adapted to receive a beam or group of ions and to convert or partition the beam or group of ions such that a plurality or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 separate packets of ions are confined and/or isolated in the ion trap or ion guide at any particular time, and wherein each packet of ions is separately confined and/or isolated in a separate axial potential well fonned within the ion trap or ion guide.

The mass spectrometer preferably further comprises means arranged and adapted to urge at least some ions upstream and/or downstream through or along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial length of the ion trap or ion guide in a mode of operation.

-36 -The mass spectrometer preferably further comprises first transient DC voltage means arranged and adapted to apply one or more transient DC voltages or potentials or one or more transient DC voltage or potential waveforms to the electrodes forming the ion trap or ion guide in order to urge at least some ions upstream and/or downstream along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial length of the ion trap or ion guide.

The mass spectrometer preferably further comprises AC or RF voltage means arranged and adapted to apply twoor more phase-shifted AC or RF voltages to electrodes fonning the ion trap or ion guide in order to urge at least some ions upstream and/or downstream along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial length of the ion trap or ion guide.

The mass spectrometer preferably further comprises means arranged and adapted in a mode of operation to maintain at least a portion of the ion trap or ion guide at a pressure selected from the group consisting of: (i) > 0.0001 mbar; (ii) > 0.001 mbar; (iii) 0.01 mbar; (iv) > 0.1 mbar; (v) > 1 mbar; (vi) > 10 mbar; (vii) > 1 mbar; (viii) 0.0001-100 mbar; and (ix) 0.001-10 mbar.

The collision, fragmentation or reaction device may comprise a quadrupole rod set, an hexapole rod set, an octopole or higher order rod set or an ion tunnel comprising a plurality of electrodes having apertures through which ions are transmitted. The apertures are preferably substantially the same size. The collision, fragmentation or reaction device may, more generally, comprise a plurality of electrodes connected to an AC or RF voltage supply for radially confining ions within the collision, fragmentation or reaction device. n axial DC voltage gradient may or may not be applied along at least a portion of the length of the ion tunnel collision, fragmentation or reaction device. The collision, fragmentation or reaction device may be housed in a housing or otherwise arranged so that a substantially gas-tight enclosure is formed around the collision, fragmentation or reaction device apart from an optional -37 -aperture to admit ions and an aperture for ions to exit from and optionally a port for introducing gas. A gas such as helium, argon, nitrogen, air or methane may be introduced into the collision, fragmentation or reaction device.

Other arrangements are also contemplated wherein the collision, fragmentation or reaction device is not repeatedly switched, altered or varied between a high fragmentation or reaction mode and a low fragmentation or reaction mode. For example, the collision, fragmentation or reaction device may be left permanently ON and arranged to fragment orreact iQfls received within the collision, fragmentation or reaction device. An electrode or other device may be provided upstream of the collision, fragmentation or reaction device. A high fragmentation or reaction mode of operation would occur when the electrode or other device allowed ions to pass to the collision, fragmentation or reaction device. A low fragmentation or reaction mode of operation would occur when the electrode or other device caused ions to by-pass the collision, fragmentation or reaction device and hence not be fragmented or reacted therein.

Other embodiments are also contemplated which would be useful where particular parent or precursor ions could not be easily observed since they co-eluted with other commonly observed peptide ions. In such circumstances the expression level of fragment, product, daughter or adduct ions is compared between two samples.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; -38 -repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from the first sample, the first fragment, product, daughter or adduct ions having a first mass to charge ratio; automatically determining the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from the second sample, the second fragment, product, daughter or adduct ions having the same first mass to charge ratio; and comparing the intensity of the first fragment, product, daughter or adduct ions with the intensity of the second fragment, product, daughter or adduct ions; wherein if the intensity of the first fragment, product, daughter or adduct ions differs from the intensity of the second fragment, product, daughter or adduct ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; and wherein the collision, fragmentation or reaction device is selected from the group consisting of: (1) a Surface Induced Dissociation (uSID) fragmentation device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Capture Dissociation fragmentation device; (iv) an Electron Collision or Impact Dissociation fragmentation device; (v) a Photo Induced Dissociation ("PID") fragmentation device; (vi) a Laser Induced Dissociation fragmentation device; (vii) an infrared radiation induced dissociation device; (viii) an ultraviolet radiation induced dissociation device; (ix) a nozzle-skimmer interface fragmentation device; (x) an in-source fragmentation device; (xi) an ion-source -39 -Collision Induced Dissociation fragmentation device; (xii) a thermal or temperature source fragmentation device; (xiii) an electric field induced fragmentation device; (Xiv) a magnetic field induced fragmentation device; (xv) an enzyme digestion or enzyme degradation fragmentation device; (xvi) an ion-ion reaction fragmentation device; (xvii) an ion-molecule reaction fragmentation device; (xviii) an ion-atom reaction fragmentation device; (xix) an ion-metastable ion reaction fragmentation device; (xx) an ion-metastable molecule reaction fragmentation device; (xxi) an ion-metastable atom reaction fragmentation device; (xxii) an ion-ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxv) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxvi) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxvii) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.

According to another aspect of the present invention there is provided a method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmex3tation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the first sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying the collision, fragmentation or reaction device between a first mode wherein at least some of the parent or precursor ions from the second sample are fragmented or reacted into one or more fragment, product, daughter or -40 -adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from the first sample, the first fragment, product, daughter or adduct ions having a first mass to charge ratio; automatically determining the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from the second sample, the second fragment, product, daughter or adduct ions having the same first mass to charge ratio; determining a first ratio of the intensity of the first fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in the first sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in the first sample; determining a second ratio of the intensity of the second fragment, product, daughter or adduct ions to the intensity àf other parent or precursor ions in the second sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in the second sample; comparing the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or precursor ions and/or the second Pc rent or precursor ions are considered to be parent or precursor ions of interest; and wherein the collision, fragmentation or reaction device is selected from the group consisting of: Ci) a Surface Induced Dissociation (TSID) fragmentation device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Capture Dissociation fragmentatj device; (iv) an Electron Collision or Impact Dissociation fragmentation device; Cv) a Photo Induced Dissociation (UPIDU) fragmentation device; (vi) a Laser Induced Dissociation fragmentatjo device; (vii) an infrared radiation induced dissociation device; (viii) an ultraviolet radiation induced dissociation device; (ix) a nozzle-sjcjjpjner interface fragmentation -41 -device; (x) an in-source fragmentation device; (xi) an ion-source Collision Induced Dissociation fragmentaj device; (xii) a thermal or temperature Source fragnientatjor device; (xiii) an electric field induced fragmentation device; (Xiv) a magnetic field induced fragmentajo device; (xv) an enzyme digestion or enzyme degradation fragmentation device; (xvi) an ion-ion reaction fragmentation device; (Xvii) an ion-molecule reaction frgmentajo device; (xviii) an ion-atom reaction fragmentation device; (xix) an ion-znetastable ion reaction fragmentation device; (xx) an ion-metastable molecule reaction fragmentajo device; (xxi) an ion-metastable atom reaction fragmentation device; (xxii) an ion-ion reaction device for reacting ions to form adduct or product 1On; (xxiii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxv) an iOn-metastable ion reaction device for reacting ions to form adduct or product ions; (xxvi) an ion-metasta,1e molecule reaction device for reacting ions Lo form adduct or product IOnS; and (xxvii) an ion-xnetastable atom reaction device for reacting ions to form adduct or product ions.

According to another aspect of the present invention there is provided a mass spectrometer comprising: a col1isio, fragmentation or reaction device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at ledst some parent or precursor ions are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in use: (i) determines the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from a first sample, the first fragment, product, daughter or adduct ions having a first mass to charge ratio; (ii) determines the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions -42 -from a second sample, the second fragment, product, daughter or adduct ions having the same first mass to charge ratio; and (iii) compares the intensity of the first fragment, product; daughter or adduct ions with the intensity of the second fragment, product, daughter or adduct ions; wherein if the intensity of the first fragment, product, daughter or adduct ions differs from the intensity of the second fragment, product, daughter or adduct ions by more than a predetermined amount then either the first parent or precursor ions and/or the second parent or precursor ions are-considered to be parent or precursor ions of interest; and wherein the collision, fragmentaj or reaction device is selected from the group Consisting of: (i) a Surface Induced Dissociation (sIDN) fragmentaj device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Capture Dissociation fragmentation device; (iv) an Electron Collision or Impact Dissociation fragmentation device; (v) a Photo Induced Dissociation (PIDu) fragmentati device; (vi) a Laser Induced Dissociation fragmentation device; (vii) an infrared radiation induced dissociation device; (Viii) an ultraviolet radiation induced dissociation device; (ix) a nozzleskjninier interface fragmentation device; (x) an in-source fragmentation device; (xi) an ion-source Collision Induced Dissociation fragmentation device; (xii) a thernia].

-or temperature source fragmentaj11 device; (Xiii) an electric field induced fragmentation device; (xiv) a magnetic field induced fragmentatjo device; (xv) an enzyme digestion or enzyme degradation fragmentation device; (xvi) an ion--jon reaction fragmentation device; (xvii) an ion-molecule reaction frcgmentatjon device; (xviii) an ion-atom reaction fragmentation device; (xix) an iOfl-metagtle ion reaction fragmentaj device; (xx) an ion-metastable molecule reaction fragmenta device; (xxi) an ion-metast]. atom reaction fragmentaj device; (xxii) an ion-jon reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-atom reaction device for reacting ions to form adduct or product -43 -iOns; (xxv) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxvi) an ion-ntetastable molecule reaction device for reacting ions to form adduct or product ions; and (xxvii) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.

According to another aspect Lf the present invention there is provided a mass spectrometer comprising: a collision fragmentation o reaction device repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from a first sample, the first fragment, product, daughter or adduct ions having a first mass to charge ratio; (ii) determines the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from a second sample, the second fragment, product, daughter or adduct ions having the same first mass to charge ratio; (iii) determines a first ratio of the intensity of the first fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in the first sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in the first sample; (iv) determines a second ratio of the intensity of the second fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in the second sample or with the intensity of other fragment, product, daughter or adduct lOflS derived from other parent or precursor ions in the second sample; and (i,) compares the first ratio with the second ratio; wherein if the first ratio differs from the second ratio by more than a predetermined amount then either the first parent or -44 -precursor ions and/or the second parent or precursor ions are considered to be parent or precursor ions of interest; and wherein the collision, fragmentaj or reaction device is selected from the group Consisting of: (i) a Surface Induced Dissociation (USIDI) fragmentation device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Capture Dissociation fragmentation device (iv) an Electron Collision or Impact Dissociation fragmentatjo device; (v) a Photo Induced Dissociation (PID") fragmentation device; (vi) a Laser Induced 10. Dissociation fragmentation device; (vu) an infrared radiation induced dissociation device; (viii) an ultraviolet radiation induced dissociation device; (ix) a nozzle--skimmer interface fragmentation device; (x) an in-source fragmentation device; (xi) an ion-source Collision Induced Dissociation fragmentation device; (xii) a thermal or temperature source fragmentation device; (xiii) an electric field induced fragmentation device; (xiv) a magnetic field induced fragmentj device; (xv) an enzyme digestion or enzyme degradation fragmentation device; (xvi) an ion-ion reaction fragmentation device; (xvii) an ion-molecule reaction fragmentation device; (xviii) an ion-atom reaction fragmentation device; (xix) an ion-metastable ion reaction fragmentation device; (xx) an ion-metast,1e molecule reaction fragmentation device; (xxi) an ion-metastable atom reaction fragmentation device; (xxii) an ion-ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxv) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxvi) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxvii) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.

It will be apparent that the above described embodiments which relate to comparing the expression level of fragment, product, daughter or adduct ions rather than parent or precursor ions either directly or indirectly may employ the method and apparatus relating -45 -to the preferred embodiment. Thexefore, the same preferred features which are recited with respect to the preferred embodiment may also be used with the embodiments which relate to comparing the expression level of fragment, product, daughter or adduct ions.

If parent or precursor ions having a particular mass to charge ratio are expressed differently in two different samples, then according to the preferred embodlirient further investigation of the parent or precursor ions of interest then occurs. This further investigation may comprise seeking to identify the parent or precursor ions of interest which are expressed differently in the two different samples. In order to verify that the parent or precursor ions whose expression levels are being compared in the two different samples really are the same ions, a number of checks may be made.

Measurements of changes in the abundance of proteins in complex protein mixtures can be extremely informative For example, changes to the abundance of proteins in cells, often referred to as the protein expression level, could be due to different cellular stresses, the effect of stimuli, the effect of disease or the effect of drugs. Such proteins may provide relevant targets for study, screening or intervention. The identification of such proteins will normally be of interest. Such proteins may be identified by the method of the preferred embodiment Therefore, according to the preferred enthodin'ient a new criterion for the discovery of. parent or precursor ions of interest is based on the quantification of proteins in two different samples.

This requires the determination 01 the relative abundances of their peptide products in two or more scunpies. However, the determination of relative abundance requires that the same peptide ions must be compared in the two (or more) different samples and ensuring that this happens is a non-trivial problem. Hence, it is necessary to be able to recognise and preferably identify the peptide ion to the extent that it can at least be uniquely recognised Within the sample.

Such peptide ions may be adequately recognised by measurement of the mass of the parent or precursor ion and by measurement of the mass to charge ratio of one or more fragment, product,' daughter or adduct -46 -ions derived from that parent or precursor ion. The specificity with which the peptides may be recognised may be increased by the detexinatjon of the accurate mass of the parent or precursor ion and/or the accurate mass of one or more fragment, product, daughter or adduct ions.

The same method of recognisjrg parent or precursor ions in one sample is also Preferably used to recognise the same parent or precursor ions in another sample and this enables the relative abundances of the parent or precursor ions in the two different samples to be measured.

Measurement of relative abundances allows discovery of proteins with a signjfjcan change or difference in expression level of that protein. The same data allows identification of that protein by the method already described in which several or all fragment, product, daughter or adduct iOflS associated with each such peptide product ion is discovered by closeness of fit of their respective elution times.

Again, the accurate measurent of the masses of the parent or precursor ion and associated fragment, product, daughter or adduct ions substantially improves the specificity and confidence with which the protein may be identified.

The specificity with which the peptides may be recognised may also be increased by comparison of retention times. For exalnp].e, the HPLC or CE retention or elution times will be measured as part of the procedure for associating fragment, product, daughter or adduct ions with parent or precursor ions, and these elution times may also be Compared for the two or more samples. The elution times may be used to reject measurements where they do not fall within a pre-defined time difference of each other. Alternatively, retention times may be used to confirm recognition of the same peptide when they do fall within a predefined window of each other. Commonly there may be some redundancy if the parent or precursor ion accurate mass, one or more fragment, product, daughter or adduct ion accurate masses, and the retention times are all measured and compared. In many instances just two of these measurenenLs will be adequate to recognise the same peptjde parent or precursor ion in the two or more samples. For -47 -example, measurement of just the accurate parent or precursor ion mass to charge ratio and a fragment, product, daughter or adduct ion mass to charge ratio, or the accurate parent or precursor ion mass to charge ratio and the retention time, may well be adequate.

Nevertheless the additional measurements may be used to confirm the recognition of the same parent peptide ion.

The relative expression leveLs of the matched parent peptide ions may be quantified by measuring the peak areas relative to an internal standard.

--10 The preferred embodiment does not require any interruptj. to the acquisition of data and hence LS Particularly suitable for quantitative applications Accorthng to an embodiment one or more endogenous peptides common to both mixtures which are not changed by the experimental state of the samples may used as an internal standard or standards for the relative peak area measurements According to another embodiment an internal standard may be added to each sample where no such internal standard is present or can be relied UpOn. The internal standard, whether naturally present or added, may also serve as a chrolnatographi0 retention time standard as well as a mass accuracy standard.

Ideally more than one peptide parent or precursor ion may be measured for each protein to be quantified. For each peptide the same means of recognition is preferably used when comparing intensities in each of the different samples. The measurements of different peptides serves to validate the relative abundance measurements Furthermore the measurements from several peptides provides a means of deter-mining the average relative abundance, and of determining the relative signifcanc of the measurements.

According to one embodiment all parent or precursor ions may be identified and their relative abundances determined by comparison of their intensities to those of the:,ame identity in one or more other samples.

In another embodiment the relative abundance of all parent or precursor ions of interest, discovered on the basis of their relationship to a predetermined fragment, product, daughter or adduct -48 -ion, may be determined by compari,on of their intensities to those of the same identity in one or more other samples.

In another embodiment the rdtjve abundance of all parent or precursor ions of interest, discovered on the basis of their giving rise to a predetermined mass loss, may be determined by comparison of their intensities to those of the same identity in one or more other samples.

In another embodiment it may be merely required to quantify a protein already identified The protein may be in a complex mixture, and the same means for separation and recognitjo may be used as that already described. Here it is only necessary to recognise the relevant peptide product or products and measure their intensities in one or more samples. The basis for recognition may be that of the peptide parent or precursor ion mass or accurate mass, and that of one or more fragment, product, daughter or adduct ion masses, or accurate masses. Their retention times may also be compared thereby providing a means of confirming tie recognition of the same peptide or of rejecting unmatched peptides The preferred embodiment is dpplicable to the study of proteomjcs. However, the same methods of identification and quantifjcajo may be used in other areas of analysis such as the Study of metabolomjcs The method is appropriate for the analysis of mixtures where different components of the mixture are first separated or Partially separated by a means such as chromitogr.aphy that causes Components to elute Sequentially The source of ions may preferably yield mainly molecular ions or pseudo-molecular ions and relatively few (if any) fragment, product, daughter or adduct iOflS. Examples of such sources include atmospheric pressure ionjsatlon sources (e.g. Electrospray and APCI) and Matrix Assisted Laser Desorptjon lonisation (MALDI).

If the two main operating inoces of the collision, fragmentation or reaction device are suitably set, then parent or precursor ions can be recognised by virtue of the fact that they will be relatively more intense in the mass spectrum without substantial fragmentaj -49 -or reaction. Similarly, fragment, product, daughter or adduct ions can be recognised by virtue of the fact that they will be relatively more intense in the mass SPeCtithu with substantial fragmentation or reaction.

The mass analyser may comprise a quadrupole, Time of Flight, ion trap, magnetic sector or FT-ICp mass analyser. According to a preferred embodiment the mass analyser should be capable of determining the exact or accurate mass to charge value for ions.

This is to maxjxnjse selectivity fox detection of characteristic fragment, product, daughter or adduct ions or mass losses, and to maximjse specificity for identifjcdtjofl of proteins.

The mass analyser prefera11y samples or records the whole spectrum simultaneously. This ensures that the elution times observed for all the masses are not modified or distorted by the mass analyser, and in turn would allow accurate matching of the elution times of different masses, such as parent and fragment, product, daughter or adduct ions. It also helps to ensure that the quantitative measurents are not compromised by the need to measure abundances of transient signals.

A mass filter, preferably a quadrupole mass filter, may be provided upstrean, of the collision, fragmentation or reaction device.

The mass filter may have a highpass filter characteristic and, for exanip1e, be arranged to transmit ions having a mass to charge ratio greater than or equal to 100, 150, 200, 250, 300, 350, 400, 450 or 500. Alternatively, the mass filter may have a lowpass or bandpass filter characteristic An ion guide may be provided upstream of the collision, fragmentation or reaction device. The ion guide may comprise either a hexapole, quadrupole octopole or higher order tnultipo].e rod set.

In another embodiment the ion guide may comprise an ion tunnel ion guide comprisi.rig a plurality of electrodes having apertures through which ions are transmitted in use. Preferably, at least 90% of the electrodes have apertures which are substantially the same size.

Alternatively, the ion guide may comprise.a plurality of ring -50 -electrodes having substantially tapering internal diameters (ion funne].N).

Parent or precursor ions tllc*L belong to a particular class of parent or precursor ions, and which are recognjsab].e by a characteristic fragment, product, daughter or adduct ion or characteristic neutral loss are traditionally discovered by the methods of parent or precursor ion scanning or constant neutral loss scanning. Previous methods for recording parent or precursor ion scans or constant neutral loss scans involve scanning one or both -* 10 quadrupoles in a triple gliadrupole mass spectrometer, or scanning the quadrupo].e in a tandem quadrupolo orthogonal TOF mass spectrometer, or scanning at least one element in other types of tandem mass spectrometers As a consequence these methods suffer from the low duty cycle associated with scanning instruments. As a further consequence, information may be discarded and lost whilst the mass spectrometer is Occupied recording a parent or precursor ion scan or a Constant neutral loss scan. As a further consequence these methods are not appropriate for use where the mass spectrometer is required to analyse substances eluting directly from gas or liquid chromatography equipment.

According to the preferred embodiment, a tandem quadrupole orthogonal TOF mass spectrometer in used in a way in which parent or precursor ions of interest are discovered using a method in which sequentjai low and high collision energy mass spectra are recorded.

The switching, altering or varying back and forth is preferably not interrupted. Instead a complete set of data is acquired, and this is then processed afterwards. Fragment, product, daughter or adduct ions may be associated with parent or precursor ions by Closeness of fit of their respective elution times. In this way parent or precursor ions of interest may be confirmed or otherwise without interrupting the acquisition of data, and information need not be lost.

According to one embodiment, possible parent or precursor ions of interest may be selected on the basis of their relationship to a predetermined fragment, product, daughter or adduct ion. The predetermined fragment, product, daughter or adduct ion may comprise, f or example, immorijuxn ions from peptides, functional groups including phosphate group Po3 ions from phosphorylated peptides or mass tags which are intended to cleave from a specific molecule or class of molecule and to be subsequently identified thus reporting the presence of the specific molecule or class of molecule. A parent or precursor ion may be short listed s a possible parent or precursor ion of interest by generating a mass chroinatogram for the predetermined fragment, product, daughter or adduct ion using high fragmentation or reaction mass spectra. The centre of each peak in the mass chromatogram is then det:ennjyied together with the corresponding predetermined fragment, product, daughter or adduct ion elution time(s). Then for each peak in the predetermined fragment, product, daughter or adduct ion mass chromatogram both the low fragmentaj or reaction mass spectrum obtained immediately before the predetermined fragment, product, daughter or adduct ion elution time and the low fragmentation or reaction mass spectrum obtained immediately after the predetermined fragment, product, daughter or adduct ion elution time are interrogated for the presence of previously recognised parent or precursor ions. A mass chromatogram for any Previously recognised parent or precursor ion found to be present in both the low fragmentation or reaction mass spectrum obtained immediately before the predetermined fragment, product, daughter or adduct ion elution time and the low fragmentation or reaction mass spectrum obtained immediately after the predetermined fragment, product, daughter or adduct ion elution time is then generated and the centre of each peak in each mass chroniatogram is determined together with the corre;pondjng possible parent or precursor ion of interest elutjon time(s). The possible parent or precursor ions of interest may then be ranked according to the closeness of fit of their elutjon time with the predetermined fragment, product, daughter or adduct ion elution time, and a list of final possible parent or precursor ions of interest may be formed by rejecting Possible parent or precursor ions of interest if their elution time precedes or exceeds the predetermined fragment, product,

--

daughter or adduct ion elution time by more than a predetermined amount.

According to an alternative embodiment, a parent or precursor ion may be shortlisted as a possible parent or precursor ion of interest on the basis of it giving rise to a predetermined mass loss.

For each low fragmentaio or reac Lion mass spectrum, a list of target fragment, product, daughter or adduct ion mass to charge values that would result from the ioss of a predetermined ion or neutral particle from each Previously recognised parent or precursor ion present -ii the low fragmenta'-jon or reaction mass spectrum is generated. Then both the high fragmentaj or reaction mass spectrum obtained immediately before the low fragmentajo or reaction mass spectrum and the high fragmentaj or reaction mass spectruj obtained immediately after the low fragmentation or reaction mass spectrum are interrogated for the presence of fragment, product, daughter or adduct ions having a mass to charge value corresponding with a target fragment, product, daughter or adduct ion mass to charge value. A list of possible parent or precursor ions of interest (Optionally including their corresponding fragment, product, daughter or adduct ions) is then torrned by including in the list a parent or precursor ion if a fragment, product, daughter or adduct ion having a mass to charge value corresponding with a target fragment, product, daughter or adduct ion mass to charge value is found to be present in both the high fragmentation or reaction mass spectrum immediately before the low fragmentatjo or reaction mass spectrum and the high fragmentaj0 or reaction mass spectrum immediately after the low fragmeniaj or reaction mass spectrum. A mass loss chromatogram may then be generated based upon possible candidate parent or precursor ions and their corresponding fragment, product, daughter or adduct lOflS. The centre of each peak in the mass loss chromatogr is determjnd together with the corresponding mass loss elutjon time(s). Then for each possible candidate parent or precursor ion a mass chromatogram is generated using the low fragmentation or reaction mass spectra. A corresponding fragment, product, daughter or adduct ion mass chromatogram is also generated -53 -for the corresponding fragment, ptoduct, daughter or adduct ion. The centre of each peak in the possible candidate parent or precursor ion mass chromatogrm and the correspciiaing fragment, product, daughter or adduct ion mass chromatogr are then determined together with the corresponding possible candidate pdrent or precursor ion elution time(s) and corresponding fragment product, daughter or adduct ion elution time(s). A list of fina] candidate parent or precursor ions may then be formed by rejecting pcsib1e candidate parent or precursor ions if the elutjon time of a possible candidate parent or precursor ion precedes or exceeds he corresponding fragment, product, daughter or adduct ion elution time by more than a predetermined ainount. -Once a list of parent or precursor ions of interest has been formed (which Preferably comprises only some of the originally recognised parent or precursor ions and possible parent or precursor ions of interest) then each parent or precursor ion of interest can then be identified.

Identification of parent or precursor ions may be achieved by making use of a combination of information. This may include the accurately determined mass or mass to charge ratio of the parent or precursor ion. it may also include the masses or mass to charge ratios of the fragment, product, dcughter or adduct ions. In some instances the accurately determined masses or mass to charge ratios of the fragment, product, daughter or adduct ions may be preferred.

It is known that a protein may be Identified from the masses or mass to charge ratios, preferably the exact masses, of the peptide products from proteins that have been enzymatically digested. These may be compared to those expected from a library of known proteins.

It is also known that when the resuLts of this comparison suggest more than one possible protein then the ambiguity can be resolved by analysis of the fragments of one or more of the peptides. The preferred embodiment allows a mixture of proteins, which have been enzymatically digested, to be identified in a single analysis. The masses or mass to charge ratios, or exact masses or mass to charge ratios, of all the peptjdes and thej.r associated fragment, product, -54 -daughter or adduct ions may be sea cched against a library of known proteins. Alternatively the peptLde masses or mass to charge ratios, or exact masses or mass to charge ratios, may be searched against the library of known prote.ns, and where more than one protein is suggested the correct protein may be confirmed by searching for fragment, product, diughter or adduct ions which match those to be expected from the relevant peptides from each candidate protein.

The step of identifying each parent or precursor ion of interest Preferably comprises reca1ing the elution time of the parent or precursor ion of interesu, generating a list of possible fragment, product, daughter or adduct ions which comprises previously recognised fragment, product, daughter or adduct ions which are present in both the low fragmentat or reaction mass spectrum obtained immediately before the elution time of the parent or precursor ion of interest and the ow fragmentation or reaction mass spectrum obtained immediately afte the elution time of the parent or precursor ion of interest, generatng a mass chromatogram of each possible fragment, product, daught(r or adduct ion, determining the centre of each peak in each possible fragment, product, daughter or adduct ion mass chroxnatogr, and determining the corresponding possible fragment, product, daughtcr or adduct ion elutjon time(s).

The possible fragment, product, daghter or adduct ions may then be ranked according to the closeness of fit of their elution time with the elutjon time of the parent or precursor ion of interest. A list of fragment, product, daughter or cidduct ions may then be formed by rejecting fragment, product, daughLer or adduct ions if the elution time of the fragment, product, daughter or adduct ion precedes or exceeds the elutjon time of the parent or precursor ion of interest by more than a predetermjne amount..

The list of fragment, product daughter or adduct ions may be yet further refined or reduced by eneratjng a list of neighbouring parent or precursor ions which are present in the low fragmentation or reaction mass spectrum obtained nearest in time to the elution time of the final candidate parent or precursor ion. A mass -. 55 -chroniatogram of each parent or precursor ion contained in the list is then generated and the centre of eoch mass chromatogram is determined along with the correspondjr1g neighi)ourjng parent or precursor ion elutjon time(s). Any fragient, product, daughter or adduct ion having an elution time which corresponds more closely with a neighbouring parent or precursor ion elution time than with the elution time of a parent or precur:-or ion of interest may then be rejected from the list of fragment product, daughter or adduct ions.

Fragment, daughter, product or adduct ions may be assigned to a parent or precursor ion according.o the closeness of fit of their elution times, and all fragment, pioduct, daughter or adduct ions which have been associated with the parent or precursor ion may be listed.

An alternative embodiment which involves a greater amount of data processing but yet which is intrinsically simpler is also contemplated Once parent and fraqment, product, daughter or adduct ions have been identified, then a parent or precursor ion mass chromatogram for each recognised parent or precursor ion is generated. The centre of each. peak in the parent or precursor ion mass chromatogram and the Corresponding parent or precursor ion elution time(s) are then determineci. Similarly, a fragment, product, daughter or adduct ion mass chromat:ogram for each recognised fragment, product, daughter or adduct ion is generated, and the centre of each peak in the fragrnen., product, daughter or adduct ion mass chromatogram and the corresponding fragment, product, daughter or adduct ion elutjon time(s) are then determined. Rather than then identifying only a sub-set of the iecognjsed parent or precursor ions, all (or nearly all) of the recognised parent or precursor ions are then identified. Fragment ion are assigned to parent or precursor ions according to the closeness of fit of their respective elution times and all fragment, product, daughter or adduct ions which have been associated with a parent or precursor ion may then be listed.

Passing ions through a mass filter, preferably a quadrupole mass filter, prior to being passed to the Collision, fragmentation or -56 -reaction device presents an alterntive or an additional method of recognising a fragment, product, diughter or adduct ion. A fragment, product, daughter or adduct ion my be recognised by recognising ions in a high fragmentation or reactioi mass spectrum which have a mass to charge ratio which is not transmitted by the collision, fragmentaj0 or reaction device i.e. fragment, product, daughter or adduct ions are recognised by virt..e of their having a mass to charge ratio falling outside of the transmission window of the mass filter.

If the ions would not be transmitted by the mass filter then they must have been produced in the coijision, reaction device.

Various embodinients of the present invention will now be described, by way of example only, and with reference to the accompanying drawings in which: Fig. 1 is a schematic drawinc of a pref erred mass spectrometer; Fig. 2 shows a schematic of valve switching arrangement during sample loading and desaltin( and the inset shows desorption of a sample from an analytical column, Fig. 3A shows a fragment or daughter ion mass spectrum and Fig. 38 shows the corresponding parent or precursor ion mass spectrum obtained when a mass filter upstrejn of a collision cell was arranged so as to transmit ions having a mass to charge ratio > 350 to the Col1jjo cell; Fig. 4A shows a mass chromatc,gram of a parent or precursor ion, Fig. 48 shows a mass chromatogram of a parent or precursor ion, Fig. 4C shows a mass chromatogram of a parent or precursor ion, Fig. 4D shows a mass chromatogram of a frdqrflent or daughter ion and Fig. 4E shows a mass chroxnatogram of a fra.,ment or daughter; Fig. 5 shows the mass chromatograms of Figs. 4A-E superimposed upon one another; Fig. 6 shows a mass chromatogram of the Asparagine invnoniujn ion which has a mass to charge ratio oi 87.04; Fig. 7 shows a mass spectrum of the peptide ion T5 derived from AD1I which has the sequence ANELLINVK and a molecular weight of 1012.59; -57 -Fig. 8 shows a mass spectrum of a tryptic digest of f3-Casein obtained when a colljsjori cell was in a low fragmentajo mode; Fig. 9 shows a mass spectruj of a tryptic digest of -Casein obtained when a collision cell was in a high fragmentation mode; Fig. 10 shows a processed arid expanded view of the mass spectrum shown in Fig. 9; Fig. hA shows a mass chromatgram of an ion from a first sample having a mass to charge rato of 880.4, Fig. 11B shows a similar mass chroinatogram of the same ion from a second sample, Fig. lie shows a mass chromatogram-of an ion from a first sample having a mass to charge ratio of 582.3 and Fig. liD shows a similar mass chromatogram of the same ion from ci second sample; Fig. 12A shows a mass spectruri recorded from a first sample and Fig. 12B shows a corresponding mas spectri.u recorded from a second sample which is similar to the fir,t sample except that it contains a higher concentration of the digest products of the protein Casein which is cormuon to both samples; Fig. 13 shows the mass spectrum shown in Fig. 12A in more detail and the insert shows an expanded part of the mass spectrum showing isotope peaks at mass to charge ratio 880.4; and FigS. 14 shows the mass spectrirn shown in Fig. 12B in more detail and the insert shows an expanded part of the mass spectrum showing isotope peaks at mass to charge ratio 880.4.

A pref erred embodiment will now be described with reference to Fig. 1. A mass spectrometer 6 is shown which comprises an ion source 1, preferably an Electrospray lorlisation source, an ion guide 2 arranged downstream of the ion soulce 1, a quadrupole mass filter 3, a collision, fragmentaj or react ion device 4 and an orthogonal acceleration of Flight mass aralyser 5 incorporating a reflectron. The ion guide 2 and mass filter 3 may be omitted if necessary. The mass spectrometer b is preferably interfaced with a chromatograph, such as a liquid chlomatograph (not shown) so that the sample entering the ion source 1 may be taken from the eluent of the liquid chromatograph. 58 -

The qliadrupole mass filter 3 is Preferably disposed in an evacuated chamber which is maintained at a relatively low pressure e.g. less than 1O mbar. The rod iiectrodes comprising the mass filter 3 are Preferably coruected to a power supply which generates both RF and DC potentials which determine the mass to charge value transmission window of the mass fi ter 3.

The CO1ljj fraginentaj01 r reaction device 4 preferably comprises a Surface Induced Dissoc:ation (SIDu) fragmentjo device, an Electron Transfer Dissoc:jatjon fragmentation device or an Electron Capture Dissociation fragnientajo device.

According to an embodiment thu CollIsion, fragmentajo or reaction device 4 may comprise an Hiectron Capture Dissociation fragmentation device. According to this embodiment multiply charged analyte ions are Preferably caused to interact with relatively low energy electrons. The electrons p.eferab].y have energies of < 1 eV or 1-2 eV. The electrons are preferably confined by a relatively strong magnetic field and are directed so that the electrons collide with the analyte Ions which are preferably confined within an RF ion guide which IS preferably arranged within the fragmentaj device 4.

An AC or RF voltage is preferably opplied to the electrodes of the RF ion guide so that a radial pseudo-potential well is preferably created which Preferably acts to confine ions radially within the ion guide so that the ions can interact with the low energy electrons.

According to another einbodjmeiit the Colljjo, fragmenaj or reaction device 4 may comprise an Electron Transfer Dissociation fragmenttj device. According to this embodiment positively charged analyte ions are preferably caused to interact with negatively charged reagent ions. The negatively charged reagent ions are preferably injected into an RF LOll guide or ion trap located within the Collision, fragmentatjox or reaction device 4. An AC or RF voltage IS preferably applied t. the electrodes of the RF Ion guide so that a radial pseudo-potential well is Preferably created which Preferably acts to confine loris radially within the ion guide so that the ions can interact with the negatively charged reagent ions. According to a less preferrcd embodiment negatively charged -59 -ana].yte ions may alternatively be arranged to interact with Positively charged reagent ions.

According to anothei embodimeitt the collision, fragmentation or reaction device 4 may comprise a Surface Induced Dissociation fragmentation device. According to this embodiment ions are preferably directed towards a surface or target plate with a relatively low energy. The ions may, for example, be arranged to have an energy of 1-10 eV. The surface or target plate may comprise stainless steel or more preferably the surface or target plate may comprise a metallic plate coated with a monolayer of fluorocarbon or hydrocarbon. The monolayer preferdbly comprises a self-assembled monolayer. The surface or target plate may be arranged in a plane which is substantially parallel with the direction of travel of ions through the Surface Induced Dissociation fragmentation device in a mode of operation wherein ions are not fragmented. In a mode of operation wherein it is desired to fragment ions, the ions may be deflected onto or towards the surface or target plate so that the ions impinge the surface or target plate at a relatively shallow angle with respect to the surface of target plate. Fragment ions are preferably produced as a result of the analyte ions colliding with the surface or target plate. The fragment ions are preferably directed off or away from the surface or target plate at a relatively shallow angle with respect to the surface or target plate. The fragment ions are then preferably arranged to assume a trajectory which preferably corresponds with the trajectory of ions which are transmitted through or past the Surface Induced Dissociation fragmentation device in a mode of operation wherein ions are not substantially fragmented.

The collision, fragmentation or reaction device 4 may comprise an Electron Collision or Impact Dissociation fragmentai device wherein ions are fragmented upon collisions with relatively energetic electrons e.g. wherein the electrons have > 5eV.

According to other embodiments the collision, fragmentation or reaction device 4 may comprise a Photo Induced Dissociation (uPIDN) fragmentation device, a Laser Induced Dissociation fragmentation -60 -device, an infrared radiation induced dissociation device, an ultraviolet radiation induced dissociation device, a thermal or temperature source fragmenajn device, an electric field induced fragmentaj0 device, a magnetic field induced fragmentation device, an enzyme digestion or enzyme degridatjon fragmentation device, an jon-jon reaction fragmentation device, an ion-molecule reaction fragmentaj0 device, an ion-atom reaction fragmentaj device, an ion-metastable ion reaction fragmentaj device, an ion-metastable molecule reaction fragmentaj0 device, an ion-metastable atom reaction fragmenaj device, an ion-ion reaction device for reacting ions to form adduct or product ions, an ion-molecule reaction device for reacting ions Lo form adduct or product ions, an ion-atom reaction device for react ing ions to form adduct or product ions, an iOfl-metastable ion reaction device for reacting ions to form adduct or product ions, an ion-met(13tab1e molecule reaction device for reacting ions to form adduct OL product ions or an ion-metastajle atom reaction device for reacting ions to form adduct or product ions.

According to an embodiment the collision, fragmentation or reaction device may form part ot the ion source 1. For example, the Collision, fragmentaj0 or reaction device may comprise a nozzle-skimmer interface fragmentaj device, an in-source fragmentatj device or an ion-source Collision Induced Dissociation fragmentation device.

The collision fragmentation or reaction device 4 may Comprise either a quadrupole or hexapole rod set which may be enclosed in a substantially gas-tight casing (other than having a small ion entrance and exit orifice) into which a gas such as helium, argon, nitrogen, air or methane may be introduced at a pressure of between l0 and 10 inbar, further preferably io mbar to 10 inbar.

Suitable AC or RF potentials for the electrodes comprising the Collision, fragmentation or reaction device 4 are provided by a power Supply (not shown).

Ions generated by the ion source 1 are transmitted by the ion guide 2 and pass via an interchamber orif ice 7 into vacuum chamber 8.

-61 -Ion guide 2 is preferably maintained at a pressure intermediate that of the ion source 1 and the vacuun chamber 8. In the embodiment shown, ions maybe mass filtered by mass filter 3 before entering the preferred Collision, fragmentation or reaction device 4. However, the mass filter 3 is an optional feature of this embodiment. Ions exiting from the collision, fragmentation or reaction device 4 or which have been transmitted through the Collision, fragmentation or reaction device 4 preferably pass to a mass analyser which preferably comprises a Time of Flight mass analyser 5. Other ion optical components, such as further ion guides and/or electrostatic lenses, may be provided which are not shown in the figures or described herein. Such components may be used to maximjse ion transmission between various parts or stages of the mass spectrometer. Various vacuum pumps (not shown) may be provided for maintaining optimal vacuum conditions. The Time of Flight mass analyser 5 Incorporating a reflectron operates in a known way by measuring the transit time of the ions comprised in a packet ot ions so that their mass to charge ratios can be determined.

A control means (not shown) preferably provides control signals for the various power supplies (not shown) which respectively provide the necessary operating potentials for the ion source 1, the ion guide 2, the quadrupole mass filter 3, the collision, fragmentation or reaction device 4 and the Time of Flight mass analyser 5. These control signals preferably determine the operating parameters of the mass spectrometer, for example the mass to charge ratios transmitted through the mass filter 3 and the operation of the analyser 5. The control means may comprise a computer (not shown) which may also be used to process the mass spectral data acquired. The computer may also display and store mass spectra produced by the mass analyser 5 and receive and process commands from an operator. The control means may be set to perform automatically various methods and make various determinations without operator intervention, or may optionally require operator input at various stages.

The control means is Preferably arranged to switch, vary or alter the collision, fragmentatjc or reaction device 4 back and -62 - forth between at least two different modes. If the collision, fragmentaj or reaction device 4 comprises an Electron Capture Dissociation fragmencajo device then the electron source or beam may be Switched ON in a first mode of operation and may be switched 0FF in a second mode of operation it the collision, fragmentation or reaction device 4 comprises an Electron Transfer Dissociation fragmentaj device 4 then reagent ions may be injected into an ion guide or ion trap comprising analyte ions in a first mode of operation and substantially no reagent ions may be injected into the ion guide or ion trap in a second mode of operation. If the collision, fragmentaj or reaction device 4 comprises a Surface Induced Dissociation fragmentation device then the analyte ions may be directed so that they collide or impinge upon the surface or target plate in a first mode of operation and the analyte ions may be directed straight past the surface or target plate in a second mode of operation so that the analyte ions do not collide or impinge upon the surface of target plate.

In one embodiment the Control means may switch, alter or vary between modes approximately every second. When the mass spectrometer 6 is used in Conjunction with an ion source 1 being provided with an eluent separated from a mixture by means of liquid or gas chromatography, the mass spectrometer 6 may be run for several tens of minutes over which period of time several hundred high and low fragmentatj or reaction mass spectra may be obtained.

At the end of the experimental run the data which has been obtained is preferably analysed and parent or precursor ions and fragment, product, daughter or adduct ions can be recognised on the basis of the relative intensity of a peak in a mass spectrum obtained when the collision, fragmentation or reaction device 4 was in one mode compared with the intensity of the same peak in a mass spectrum obtained approximately a second later in time when the collision, fragmentation or reaction device 4 was in the second mode.

According to an embodiment, mass chromatograms for each parent and fragment, product, daughter or adduct ion are generated and 63 -fragment, product, daughter or adduct ions are assigned to parent or precursor ions on the basis of their relative elution times.

An advantage of this method is that since all the data is acquired and subsequently processed then all fragment, product, daughter or adduct ions may be associated with a parent or precursor ion by closeness of fit of their respective elution times. This allows all the parent or precursor ions to be identified from their fragment, product, daughter or adduct ions, irrespective of whether or not they have been discovered by the presence of a characteristic fragment, product, daughter or adduct ion or characteristic neutral loss'.

According to another embodiment an attempt maybe made to reduce the number of parent or precursor ions of interest. A list of possible (i.e. not yet finalised) parent or precursor ions of interest may be formed by looking for parent or precursor ions which may have given rise to a predetermined fragment, product, daughter or adduct ion of interest e.g. an ilnmonjuxn ion from a peptide.

Alternatively, a search may be made for parent and fragment, product, daughter or adduct ions wherein the parent or precursor could have fragmented or reacted into a first component comprising a predetermjne ion or neutral particle and a second component comprising a fragment, product, daughter.or adduct ion. Various steps may then be taken to further reduce/refine the list of possible parent or precursor ions of interest to leave a number of parent or precursor ions of interest which are then preferably subsequently identified by comparing elutjon times of the parent or precursor ions of interest and fragment, product, daughter or adduct ions. As will be appreciated, two ions could have similar mass to charge ratios but different chemical structures and hence would most likely fragment differently enabling a parent or precursor ion to be identified on the basis of a fragment, product, daughter or adduct ion.

A sample introduction system is shown in more detail in Fig. 2.

Samples may be introduced into the mass spectrometer 6 by means of a Micromass (RTh) modular CapL,C system. For example, samples may be loaded onto a Cl8 cartridge (0.3 mm x 5 mm) and desalted with 0.1% -64 -HCOOH for 3 minutes at a flow rate of 3OjlL per minute. A ten port valve may then switched such that the peptides are eluted onto the analytical COlUTff1 for separation, see inset of Fig. 2. Flow from two pumps A and B may be split to produce a flow rate through the column of approximately 200n1/min.

A preferred analytical column is a PicoFrjt (RTM) column packed with Waters (RTM) Symmetry Cl8 set up to spray directly into the mass spectrometer 6. An Electrospray potential (ca. 3kv) may be applied to the liquid via a low dead volume stainless steel union. A small -amount e.g. 5 psi (34.48 kPa) of nebulising gas may be introduced around the spray tip to aid the Electrospray process.

Data may be acquired using a mass spectrometer 6 fitted with a Z-spray (RTM) nanof low Electrospray ion source. The mass spectrometer may be operated in the positive ion mode with a source temperature of 80°C and a cone gas flow rate of 401/hr.

The instrument may be calibrated with a multi-point calibration using selected fragment, product, daughter or adduct ions that result, for example, from the fragmentation of Glu-tibrinopeptide b.

Data may be processed using the MassLynx (RTM) suite of software.

Switching a Collision Induced Decomposition fragmentation cell between two different modes of operation is not intended to fall within the Scope of the present invention. However, experimental results which were obtained according to this method will nonetheless be presented since they serve to illustrate aspects of the present invention.

Figs. 3A and 3B show respectively fragment or daughter and parent or precursor ion spectra of a tryptic digest of alcohol dehydrogenase (AD1-). The fragment or daughter ion spectrum shown in Fig. 3A was obtained by maintaining a gas collision cell at a relatively high potential around 30v which resulted in significant fragmentation of ions passing therethrough. The parent or precursor ion spectrum shown in Fig. 3B was obtained at low collision energy e.g. less than or equal to 5V. The data presented in Fig. 3B was obtained using a mass filter 3 arranged upstream of the collision cell and set to transmit ions having a mass to charge value greater -65 -than 350. The mass spectra in this particular example were obtained from a sample eluting from a liquid chromatograph, and the spectra were obtained sufficiently rapidly and close together in time so that they essentially correspond to the same component or components eluting from the liquid chromatograph.

The mass spectr shown in Fig. 3A was obtained using a Collision cell to fragment ions by Collision Induced Dissociation.

Such an approach is not intended to fall within the scope of the present invention. However, the mass spectra which were obtained and the following description relating to the processing of the mass spectral data illustrate various aspects of the present invention.

In Fig. 3B, there are several high intensity peaks in the parent or precursor ion spectrum, e.g. the peaks at 418.7724 and 568.7813, which are substantially less intense in the corresponding fragment or daughter ion spectrum shown in Fig. 3A. These peaks may therefore be recognised as being parent or precursor ions. Likewise, ions which are more intense in the fragment or daughter ion spectrum shown in Fig. 3A than in the parent or precursor ion spectrum shown in Fig. 3B may be recognised as being fragment or daughter ions. As will also be apparent, all the ions having a mass to charge value less than 350 in the high fragmentation mass spectrum shown in Fig. 3A can be readily recognised as being fragment or daughter ions on the basis that they have a mass to charge value less than 350 and the fact that only parent or precursor ions having a mass to charge value greater than 350 were transmitted by the mass filter 5 to the Colljgjon cell.

Figs. 4A-E show respectively mass chromatograi for three parent or precursor ions and two fragment or daughter ions. The parent or precursor ions were determined to have massto charge ratios of 406.2 (peak MCl), 418.7 (peak MC2') and 568.8 (peak MC3) and the two fragment or daughter ions were determined to have mass to charge ratios of 136.1 (peaks MC4M and 1MC5) and 120.1 (peak 1MC6).

It can be seen that parent or precursor ion peak MCi (mass to charge ratio 406.2) correlates well with fragment or daughter ion -66 -peak MC5 (mass to charge ratio 136.1) i.e. a parent or precursor ion with a mass to charge ratio of 406.2 seems to have fragmented to produce a fragment or daughter ion with a mass to charge ratio of 136.1. Similarly, parent or precursor ion peaks MC2 and MC3 correlate well with fragment or daughter ion peaks NC4 and MC6, but it is difficult to determine which parent or precursor ion corresponds with which fragment or daughter ion.

Fig. 5 shows the peaks of Figs. 4-E overlaid on top of one other and redrawn at a different scale. By careful comparison of the peaks of MC2, MC3, MG4 and MC6 it can be seen that in fact parent or precursor ion MC2 and fragment or daughter ion MC4 correlate well whereas parent or precursor ion MC3 correlates well with fragment or daughter ion MC6. This suggests that parent or precursor ions with a mass to charge ratio of 418.7 fragmented to produce fragment or daughter ions with a mass to charge ratio of 136.1 and that parent or precursor ions with mass to charge ratio 568.8 fragmented to produce fragment or daughter ions with a mass to charge ratio of 120.1.

This cross-correlation of mass chromatograins may be carried out using automatic peak comparison means such as a suitable peak comparison software program running on a suitable computer.

Fig. 6 show the mass chroniatogram for the fragment or daughter ion having a mass to charge ratio of 87.04 extracted from a HPIJC separation and mass analysis obtained using mass spectrometer 6. It is known that the immonjum ion for the amino acid Asparagine has a mass to charge value of 87.04. This chromatogram was extracted from all the high energy spectra recorded on the mass spectrometer 6.

Fig. 7 shows the full mass spectrum corresponding to scan number 604.

This was a low energy mass spectrum recorded on the mass spectrometer 6, and is the low energy spectruxn next to the high energy spectrum at scan 605 that corresponds to the largest peak in the mass chromatograin of mass to charge ratio 87.04. This shows that the parent or precursor ion for the Asparagine ixnmonium ion at mass to charge ratio 87.04 has a mass of 1012.54 since it shows the singly charged (M�H) ion at mass to charge ratio 1013.54, and the doubly charged (M+2n) ion at mass to charge ratio 507.27.

-67 -Fig. 8 shows a mass spectrum from a low energy spectra recorded on a mass spectrometer 6 of a tryptic digest of the protein -Casein.

The protein digest products were separated by HPLC and mass analysed.

The mass spectra were recorded on a mass spectrometer 6 operating in a MS mode and alternating between low and high collision energy in a gas collision cell for successive spectra. Fig. 9 shows a mass spectrum from the high energy spectra recorded at substantially the same time that the low energy mass spectrum shown in Fig. 8 relates to. Fig. 10 shows a processed and expanded view of the mass spectrum 10. shown in Fig. 9 above. For this spectrum, the continuum data has.----been processed so as to identify peaks and display them as lines with heights proportional to the peak area, and annotated with masses corresponding to their centroided masses. The peak at mass to charge ratio 1031.4395 is the doubly charged (M+2H) ion of a peptide, and the peak at mass to charge ratio 982.4515 is a doubly charged fr agment or daughter ion. It has to be a fragment or daughter ion since it is not present in the low energy spectrum. The mass difference between these ions is 48.9880. The theoretical mass for H3P04 is 97.9769, and the mass to charge value for the doubly charged H3P04 ion is 48.9884, a difference of only 8 ppm from that observed.

It is therefore assumed that the peak having a mass to charge ratio of 982.4515 relates to a fragment or daughter ion resulting from a peptide ion having a mass to charge of 1031.4395 losing a H3PO4 ion.

Some experimental data is now presented which illustrates the ability of the preferred embodiment to quantify the relative abundance of two proteins contained in two different samples which comprise a mixture of proteins.

A first sample contained the tryptic digest products of three proteins BSA, Glycogen Phosphorylase B and Casein. These three proteins were initially present in the ratio 1:1:1. Each of the three proteins had a concentration of 330 fmol/pl. A second sample contained the tryptic digest products of the same three proteins BSA, Clycogen Phosphorylase B and Casein. However, the proteins were initially present in the ratio 1:1:X. X was uncertain but believed to be in the range 2-3. The concentration of the proteins BSA and -68 -Glycogen Phosphorylase B in the second sample mixture was the seine as in the first sample, namely 330 fmol/pl.

The experimental protocol which was followed was that 1 p1 of sample was loaded for separation on to a HPLC column at a flow rate of 4 p1/mm. The liquid flow was then split such that the flow rate to the nano-electrospray ionisatjon source was approximately 200 ni/mm.

Mass spectra were recorded on the mass spectrometer 6. Mass spectra were recorded at alternating low and high collision energy using nitrogen Collision gas. The low-co1ljsj0 energy mass spectra were recorded at a Collision voltage of by and the high-collision energy mass spectra were recorded at a collision voltage of 33V. The mass spectrometer was fitted with a Nano-Lock-Spray device which delivered a separate liquid flow to the source which may be occasionally sampled to provide a reference mass from which the mass calibration may be Periodically validated. This ensured that the mass measurements were accurate to within an RMS accuracy of 5 ppm.

Data were recorded and processed using the MassLynx (RPM) data System.

The first sample was initially analysed and the data was used as a reference. The first sample was then analysed a further two times. The second sample was analysed twice. The data from these analyses were used to attempt to quantify the (unknown) relative abundance of Casein in the second sample.

All data files were processed automatically generating a list of ions with associated areas and high-collisjo energy spectra for each experiment. This list was then searched against the Swiss-prot protein database using the ProteinLymc (RPM) search engine.

Chroinatographic peak areas were obtained using the Waters (RPM) Apex Peak Tracking aigorjt}un. Chromatograma for each charge state found to be present were summed prior to integration.

The experimentally determined relative expression level of various peptide ions normaljsed with respect to the reference data for the two samples are given in the following tables.

-69 -BSA peptide ions I Sample 1 Sample 1 Sample 2 Sample 2 Run 1 Run 2 Run 1 Run 2 FKDLGEEHFK 0.652 0.433 0.914 0.661 HLVDEPQNLIK 0.905 0.829 0.641 0.519 KVPQVSTPTLVEVSR 1.162 0.787 0.629 0.635 LVNELTEFAJ( 1.049 0.795 0.705 0.813 LGEYGFQNALIIJJ 1.278 0.818 0.753 0.753 AEFVEVTK 1.120 0.821 0.834 0.711 Average I 1.028 0.747 0.746 0.682

I ____

[1ycogen Sample 1 Sample 1 Sample 2 Sample 2 1 Phophory].ase B Run 1 Run 2 Run 1 Run 2 LPeptiae ions VLVDLER 1.279 0.751 n/a 0.701 PNFDAFpDK 0.798 0.972 0.691 0.699 EIWGVEPSR 0.734 0.984 1.053 1.054 IJITAIGDVVNHDPWGDR 1.043 0.704 0.833 0.833 VLPNDNFFEGK 0.969 0.864 0.933 0.808 QIIEQLSSGFFSPR 0.691 n/a 1.428 1.428 VAAAFPGDVDR 1.140 0.739 0.631 0.641 Average 0.951 0.836 0.928 0.881 CASEIN -Sample 1 Sample 1 Sample 2 Sample 2 Peptide sequence Run 1 Run 2 Run 1 Run 2 EDVPSER 0.962 0.941 2.198 1.962 HQGLPQEJLNENJJLR 0.828 0.701 1.736 2.090 FFVAPFPEJFGK 1.231 0.849 2.175 1.596 Average 1.007 0.830 2.036 1.883

________________ _________________

-70 -Peptides whose sequences were confirmed by higb-co1ljsj0 energy data are underlined in the above tables. Confirmation means that the probability of this peptide, given its accurate mass and the Corresponding high-col1ji0 energy data, is largez than that of any other peptjde in the database given the current fragmentatjon or reaction model. The remaining peptides are believed to be correct based on their retention time and mass compared to those for confirmed peptides. It was expected that there would be some experimental error in the results due to injection volume errors and other effects.

When using BSA as an internal reference, the relative abundance of Glycogen PhOsphorylase B in the first Sarnp].e was determined to be 0.925 (first analysis) and 1.119 (second analysis) giving an average of 1.0. The relative abundance of Glycogen Phosphorylase B in the second sample was determined to be 1.244 (first analysis) and 1.292 (second analysis) giving an average of 1.3. These results compare favourably with the expected value of 1.

Similarly, the relative abundance of Casejn in the first sample was determined to be 0.980 (first analysis) and 1.111 (second analysis) giving an average of 1.0. The relative abundance of Casein in the second sample was determined to be 2.729 (first analysis) and 2.761 (second analysis) giving an average of 2.7. These results compare favourably with the expected values of 1 and 2-3.

The. following data relates to chromatogr and mass spectra obtained from the first and second samples. One peptide having the sequence HQGLPQETTJLR and derived from Casein elutes at almost exactly the same time as the peptide having the sequence LVNEIJTEFAJc derived from BSA. Although this is an unusual occurrence, it provided an opportunity to compare the abundance of Casein in the two different samples.

Figs. 11A-D show four mass chromatogr two relating to the first sample and two relating to the second sample. Fig. hA shows a mass chromatogram relating to the first sample for ions having a mass to charge ratio of 880.4 which corresponds with the peptide ion (N+2ii) having the sequence HQGLPQEVLNENLLR and which is derived from Casejn. Fig. 11B shows a mass chromatogram relating to the second sample which Corresponds with the same peptide ion having the sequence HQGLPQEVL TJLR which is derived from Casein.

Fig. lic shows a mass chromatogram relating to the first sample for ions having a mass to charge ratio of 582.3 which corresponds with the peptjde ion (M+2H) having the sequence LVNELPEFAK and which is derived from BSA. Fig. liD shows a mass chromatogram relating to the second sample which corresponds with the same peptide ion having the sequence LVNELTEFAJC and which is derived from BSA.

The mass chromatoams show that the peptide ions having a mass to charge ratio of mass to charge ratio 582.3 derived from BSA are present in both samples in roughly equal amounts whereas there is approximately a 100% difference in the intensity of peptide ion having a mass to charge ratio of 880.4 derived from Casein.

Fig. 12A show a parent or precursor ion mass spectrum recorded after around 20 minutes from the first sample and Fig. 12B shows a parent or precursor ion mass spectru recorded after around substantially the same time from the second sample. The mass spectra show that the ions having a mass to charge ratio of 582.3 (derived from BSA) are approximately the same intensity in both mass spectra whereas ions having a mass to charge ratio of 880.4 which relate to a peptide ion from Casein are approximately twice the intensity in the second sample compared with the first sample. This is Consistent with expectations Fig. 13 shows the parent or precursor ion mass spectrum shown in Fig. 12A in more detail. Peaks Corresponding with BSA peptide ions having a mass to charge of 582.3 and peaks corresponding with the Casein peptide ions having a mass to charge ratio of 880.4 can be clearly seen. The insert shows the expanded part of the spectrum showing the isotope peaks of the peptide ion having a mass to charge ratio of 880.4. Similarly, Fig. 14 shows the parent or precursor ion mass spectrum shown in Fig. 12B in more detail. Again, peaks corresponding with BSA peptide ions having a mass to charge ratio of 582. 3 and peaks corresponding with the Casein peptide ions having a mass to charge ratio of 880.4 can be clearly seen. The insert shows -72 -the expanded part of the spectrum showing the isotope peaks of the peptjde ion having a mass to charge ratio of 880.4. It is apparent from Figs. 12-14 and from comparing the inserts of Figs. 13 and 14 that the abundance of the peptide ion derived from Casein which has a mass spectral peak of mass to charge ratio 880.4 is approximately twice the abundance in the second sample compared with the first sample.

Although the present invention has been described with reference to pref erred 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.

Claims

-73 -8965811cJ.

Claims 1. A method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a col1jjo, fragmenajo or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying said Surface Induced Dissociation fragmentation device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying said Surface Induced Dissociation fragmentation device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from said first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from said second sample which have said same first mass to charge ratio; and comparing the intensity of said first parent or precursor ions with the intensity of said second parent or precursor ions; wherein if the intensity of said first parent or precursor ions differs from the intensity of said second parent or -74 -precursor ions by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest.
2. A method as claimed in claim 1, wherein in said first mode of operation said parent or precursor ions are directed, diverted or deflected on to said surface or target plate.
3. A method as claimed in claim 1 or 2, wherein in said second mode of operation said parent or precursor ions are not directed, diverted or deflected on to said surface or target plate.
4. A method as claimed in claim 1, 2 or 3, wherein said surface or target plate comprises a self-assembled monolayer.
5. A method as claimed in any preceding claim, wherein said surface or target plate comprises a fluorocarbon or hydrocarbon monolayer.
6. A method as claimed in any preceding claim, wherein said surface or target plane is arranged in a plane which is substantially parallel to the direction of travel of said parent or precursor ions in said second mode of operation.
7. A method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying said collision, fragmentation or reaction device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; -75 -passing parent or precursor ions from a second sample to a collision, fragmentajo or reaction device; repeatedly switching, altering or varying said collision, fragmentio or reaction device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first parent or precursor ions from said first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from said second sample which have said same first mass to charge ratio; and comparing the intensity of said first parent or precursor ions with the intensity of said second parent or precursor ions; wherein if the intensity of said first parent or precursor ions differs from the intensity of said second parent or precursor ions by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; wherein said collision, fragmentj or reaction device selected from the group Consisting of: (1) an Electron Collision or Impact Dissociation fragmentatjo device; (ii) a Photo Induced Dissociation (PID") fragmentation device; (iii) a Laser Induced Dissociation fragmentajo device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozz1e-skjer interface fragmentajo device; (vu) an in-source fragmentatj device; (Viii) an ion-source Collision Induced Dissociation fragmentatjo device; (ix) a thermal or temperature source

fragmentatj device; Cx) an electric field induced

fragmentajo device; (xi) a magnetic field induced

fragmentation device; (xii) an enzyme digestion or enzyme -76 -degradation fragmentation device; (xiii) an ion-ion reaction fragmentation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-acorn reaction fragmentation device; (xvi) an ion-metastab].e ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an ion-metastable atom reaction fragmentation device; (xix) an ion-jon reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form addt or product ions; (xxii) an jon-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxiv) an ion-Inetastable atom reaction device for reacting ions to form adduct or product ions.
8. A method of mass spectrornetry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentation device; repeatedly switching, altering or varying said Surface Induced Dissociation fragmentation device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented upon impinging upon a surface or target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device comprising a Surface Induced Dissociation fragmentatjon device; repeatedly switching, altering or varying said Surface Induced Dissociation fragmentation device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented upon impinging upon a surface or -77 -target plate to produce fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; automatically determining the intensity of first parent or precursor ions from said first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from said second sample which have said same first mass to charge ratio; determining a first ratio of the intensity of said first parent or precursor ions to the intensity of other parent or precursor ions in said first sample; determining a second ratio of the intensity of said second parent or precursor ions to the intensity of other parent or precursor ions in said second sample; and comparing said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest.
9. A method as claimed in claim 8, wherein in said first mode of operation said parent or precursor ions are directed, diverted or deflected on to said surface or target plate.
10. A method as claimed in claim 8 or 9, wherein in said second mode of operation said parent or precursor ions are not directed, diverted or deflected on to said surface or target plate.
11. A method as claimed in claim 8, 9 or 10, wherein said surface or target plate comprises a self-assembled monolayer.

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12. A method as claimed in any of claims 8-11, wherein said surface or target plate comprises a fluorocarbon or hydrocarbon monolayer.
13. A method as claimed in any of claims 8-12. wherein said surface or target plane is arranged in a plane which is substantially parallel to the direction of travel of said parent or precursor ions in said second mode of operation.
14. A method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collisjo, fragmentation or reaction device; repeatedly switching, altering or varying said collision, fragmentation or reaction device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor jong are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying said collision, fragmentation or reaction device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented or reacted to produce fragment, daughter, product or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first parent or precursor ions from said first sample which have a first mass to charge ratio; automatically determining the intensity of second parent or precursor ions from said second sample which have said same first mass to charge ratio; determining a first ratio of the intensity of said first parent or precursor ions to the intensity of other parent or precursor ions in said first sample; -79 -determining a second ratio of the intensity of said second parent or precursor ions to the intensity of other parent or precursor ions in said second sample; and comparing said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; wherein said Collision, fragmentation or reaction device selected from the group consisting of: (i) an Electron Collision or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation (P]D) fragmentation device; (iii) a Laser Induced Dissociation fragmentatjo device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmentation device; (vii) an in-source fragmentation device; (Viii) an IOfl-Source Collision Induced Dissociation fragmentaj device; (ix) a thermal or temperature source

fragmentajo device; (x) an electric field induced

fragmentajo device; (xi) a magnetic field induced

fragmenaj device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion-ion reaction fragmentajo device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastable ion reaction fragmentation device; (xvii) an ion-meta$table molecule reaction fragmentation device; (xviii) an lOn-metastable atom reaction fragmentation device; (Xix) an iofl-jon reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxii) an ion-metastab].e ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastab].e molecule reaction device for reacting ions to form adduct or product ions; and (xxiv) an ion-Inetastable atom reaction device for reacting ions to form adduct or product ions.
15. A method as claimed in any of claims 8-14, wherein either said othe.r parent or precursor ions present in said first sample and/or said other parent or precursor ions present i said second sample are endogenous to said sample.
16. A method as claimed in any of claims 8-14, wherein either said other parent or precursor ions present in said first sample and/or said other parent or precursor ions present in said second sample are exogenous to said sample.
17. A method as claimed in any of claims 8-16, wherein said other parent or precursor ions present in said first sample and/or said other parent or precursor ions present in said second sample are additionally used as a chromatographic retention time standard.
18. A method as claimed in any preceding claim, comprising automatically switching, altering or varying said collision, fragmentajo or reaction device between at least said first mode and said second mode at least once every 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 seconds.
19. A method as claimed in any preceding claim, wherein said predetermined amount is selected from the group Consisting of: (i) 1%; (ii) 10%; (iii) 50%; (iv) 100%; Cv) 150%; (vi) 200%; (vii) 250%; (viii) 300%; (ix) 350%; Cx) 400%; (xi) 450%; (xii) 500%; (xiii) 1000%; (xiv) 5000%; or (xv) 10000%.
20. A method as claimed in any preceding claim, wherein said collision, fragmentation or reaction device is maintained at a pressure selected from the group Consisting of: Ci) greater than or equal to 0. 0001 mbar; (ii) greater than or equal to 0.0005 mbar; (iii) greater than or equal to 0.001 mbar; (iv) greater than or equal to 0.005 mbar; (v) greater than or equal to 0.01 mbar; (vi) greater than or equal to 0.05 mbar; (vii) greater than or equal to 0.1 mbaz-; (viii) greater than or equal to 0.5 mbar; (ix) greater than or equal to 1 mbar; (x) greater than or equal to 5 mbar; and (xi) greater than or equal to 10 mbar.
21. A method as claimed in any preceding claim, wherein said cOllision, fragmentatj or reaction device is maintained at a pressure selected from the group Consisting of: (i) less than or equal to 10 nthar; (ii) less than or equal to 5 mbar; (iii) less than or equal to 1 mbar; (iv) less than or equal to 0.5 mbar; Cv) less than or equal to 0.1 mbar; (vi) less than or equal to 0.05 mbar; (Vii) less than or equal to 0.01 mbar; (viii) less than or equal to 0.005 mbar; (ix) less than or equal to 0.001 mbar; (x) less than or equal to 0.0005 mbar; and (xi) less than or equal to 0.0001 inbar.
22. A method as claimed in any preceding claim, wherein gas in said collIsion, fragmentatjo or reaction device is maintained at a first pressure when said collision, fragmentatjon or reaction device is in said first mode and at a second lower pressure when said colljj, fragmentation or reaction device is in said second mode.
23. A method as claimed in any preceding claim, wherein gas in sai' collision, fragmentatjo or reaction device comprises a first gas or a first mixture of gases when said collisj, fragmentation or reaction device is in said first mode and a second different gas or a second different mixture of gases when said collision, fragmentatj or reaction device is in said second mode.

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24. A method as claimed in any preceding claim, further comprising the step of.ideritifyjng said parent or precursor ions of interest.
25. A method as claimed in claim 24, wherein the step of identifying said parent or precursor ions of interest comprises determining the mass to charge ratio of said parent or precursor ions of interest.
26. A method as claimed in claim 25, wherein -the mass to charge ratio of said parent or precursor ions of interest is determined to less than or equal to 20 ppm, 15 ppm, 10 ppm or 5 ppm.
27. A method as claimed in claim 25 or 26, further comprising comparing the determined mass to charge ratio of said parent or precursor ions of interest with a database of ions and their corresponding mass to charge ratios.
28. A method as claimed in any of claims 24-27, wherein said step of identifying said parent or precursor ions of interest comprises identifying one or more fragment, product, daughter or adduct ions which are determined to result from fragmentation or reaction of said parent or precursor ions of interest.
29. A method as claimed in claim 28, wherein said step of identifying one or more fragment, product, daughter or adduct ions further comprises determining the mass to charge ratio of said one or more fragment, product, daughter or adduct ions to less than or equal to 20 ppm, 15 ppm. 10 ppm or 5 ppm.
30. A method as claimed in claim 28 or 29, wherein the step of identifying parent or precursor ions of interest comprises determining whether said parent or precursor ions of interest are observed in a mass spectrum obtained when said collision, fragmentation or reaction device is in said second mode for a -83 -certain time period and said fragment, product, daughter or adduct ions are observed in a mass spectrum obtained either immediately before said certain time period, when said Collision fragmentation or reaction device is in said first mode, or immediately after said certain time period, when said Collision, fragmentatjo or reaction device is in said first mode.
3].. A method as claimed in claims 28, 29 or 30, wherein the step of identifying said parent or precursor ions of interest comprises determining, that the elution time of said parent or precuror ions of interest is substantially the same as the pseudo-elution time of said. fragment, product, daughter or adduct ions.
32. A method as claimed in any of claims 28-31, wherein the step of identifying said parent or precursor ions of interest comprises comparing the elution profile of said parent or precursor ions of interest with the pseudo-e].ution profile of said fragment, product, daughter or adduct ions.
33. A method of mass spectrometry as claimed in any preceding claim, further comprising determining that ions are parent or precursor ions by comparing two mass spectra obtained one after the other, a first mass spectrun being obtained when said collis1o, fragmenaj0 or reaction device was in said first mode and a second mass spectruj being obtained when said Collisj, fragmentatj0 or reaction device was in said second mode, wherein ions are determined to be parent or precursor ions if a peak corresponding to said ions in said second mass spectrum is more intense than a peak correspondjng.to said ions in said first mass spectrun.
34. A method as claimed in any preceding claim, further comprising determining that ions are determined to be fragment, -84 -product, daughter or adduct ions by comparing two mass spectra obtained one after the other, a first mass spectrum being obtained when said coIljjo, fragmentation or reaction device was in said first mode and a second mass spectrum being obtained when said collision, fragmentation or reaction device was in said second mode, wherein ions are determined to be fragment, product, daughter or adduct ions if a peak corresponding to said ions in said first mass spectrwn is more intense than a peak corresponding to said ions in said second mass spectrum.
35. A method as claimed in any preceding claim, further Comprising: providing a mass filter upstream of said collision, fragmentation or reaction device wherein said mass filter is arranged to transmit ions having mass to charge ratios within a first range but to substantially attenuate ions having mass to charge ratios within a second range; and wherein ions are determined to be fragment, product, daughter or adduct ions if they are determined to have a mass to charge ratio falling within said second range.
36. A method as claimed in any preceding claim, wherein said first parent or precursor ions and said second parent or precursor ionsare determined to have mass to charge ratios which differ by less than or equal to 40 ppm, 35 ppm, 30 ppm, 25 ppm, 20 ppm, 15 ppm, 10 ppm or 5 ppm.
37. A method as claimed in any preceding claim, wherein said first parent or precursor ions and said second parent or precursor ions are determined to have eluted from a chromatography column after substantially the same elution time.
38. A method as claimed in any preceding claim, wherein said first parent or precursor ions are determined to give rise to one or more first fragment, product, daughter or adduct ions and said second parent or precursor ions are determined to give rise to one or more second fragment, product, daughter or adduct ions, wherein said one or more first fragment, product, daughter or adduct ions and said one or more second fragment, product, daughter or adduct ions have substantially the same mass to charge ratio.
39. A method as claimed in claim 38, wherein the mass to charge ratio of said one or more first fragment, product, daughter or adduct ions and said one or more second fragment, product, daughter or adduct ions are determined to differ by less than or equal to 40 ppm, 35 ppm, 30 ppm, 25 ppm, 20 ppm, 15 ppm, 10 ppm or 5 ppm.
40. A method as claimed in any preceding claim, wherein said first parent or precursor ions are determined to give rise to one or more first fragment, product, daughter or adduct ions and said second parent or precursor ions are determined to give rise to one or more second fragment, product, daughter or adduct ions and wherein said first parent or precursor ions and said second parent or precursor ions are observed in mass spectra relating to data obtained in said second mode at a certain point in time and said one or more first and second fragment, product, daughter or adduct ions are observed in mass spectra relatiiig to data obtained either immediately before said certain point in time when said collision, fragmentaj0 or reaction device is in said first mode or immediately after said certain point in time when said collision, fragmentation or reaction device is in said first mode.
41. A method as claimed in any preceding claim, wherein said first parent or precursor ions are determined to give rise to one or more first fragment, product, daughter or adduct ions and said second parent or precursor ions are determined to give rise to one or more second fragment, product, daughter or adduct ions -86 -and wherein said first fragment, product, daughter or adduct ions have substantially the same pseudo-elutjon time as said second fragment, product, daughter or adduct ions.
42. A method as claimed in any preceding claim, wherein said first parent or precursor ions are determined to give rise to one or more first fragment, product, daughter or adduct ions and said second parent or precursor ions are determined to give rise to one or more second fragment, product, daughter or adduct ions and wherein said first parent or precursor ions are determined to have an e].utjon profile which correlates with a pseudo-elutjon profile of said first fragment, product, daughter or adduct ions and wherein said second parent or precursor ions are determined to have an elution profile which correlates with a pseudo.-elutjon profile of said second fragment, product, daughter or adduct ions.
43. A method as claimed in any preceding claim, wherein said first parent or precursor ions and said second parent or precursor ions are determined to be multiply charged.
44. A method as claimed in any preceding claim, wherein said first parent or precursor ions and said second parent or precursor ions are determjnj to have the same charge state.
45. A method as claimed in any preceding claim, wherein fragment, product, daughter or adduct ions which are determined to result from the fragmentation or reaction of said first parent or precursor ions are determined to have the same charge state as fragment, product, daughter or adduct ions which are determined to result from the fragmentation or reaction of said second parent or precursor ions.
46. A method as claimed in any preceding claim, wherein said first sample and/or said second sample comprise a plurality of -87 -different biopolymers, proteins, peptides, polypeptides, oligionuc1eotj oligionucleosj, amino acids, carbohydrates, sugars, lipids, fatty acids, vitamins, hormones, portions or fragments of DNA, portions or fragments of cDNA, portions or fragments of RNA, portions or fragments of mRNA, portions or fragments of tRNA, polyc].onaj. antibodies, monoclonal antibodies, ribonucleases, enzymes, metabolites, polysaccharides, phosphorylated peptides, phosphorylated proteins, glycopeptjdes, g1ycoprotejn or steroids.
?. A method as claimed in any preceding claim, wherein said first sample and/or said second sample comprise at least 2, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, or 5000 molecules having different identities.
48. A method as claimed in any preceding claim, wherein either: (i) said first sample is taken from a diseased organism and said second sample is taken from a non-diseased organism; (ii) said first sample is taken from a treated organism and said second sample is taken from a non-treated organism; or (iii) said first sample is taken from a mutant organism and said second sample is taken from a wild type organism.
49. A method as claimed in any preceding claim, wherein molecules from said first and/or second samples are separated from a mixture of other molecules prior to being ionised by: (1) High Performance Liquid Chromatography ("}IPLC"); (ii) anion exchange; (iii) anion exchange chromatography; (iv) cation exchange; (v) cation exchange chromatography; (vi) ion pair reversed-phase chromatography; (vii) chromatography; (viii) single dimensional electrophoresjs; (ix) multi-dimensional electrophoresjs; Cx) size exclusion; (xi) affinity; (xii) reverse phase chromatography; (xiii) Capillary Electrophoresjs Chromatography ("CEC); (xiv) electrophoresis; (xv) ion mobility -88 -separation; (xvi) Field Asymmetric Ion Mobility Separation ("FAIMS); or (xvi) capillary electrophoresis.
50. A method as claimed in any preceding claim, wherein said first and second sample ions comprise peptide ions.
51. A method as claimed in claim 50, wherein said peptide ions comprise the digest products of one or more proteins.
52. A method as claimed in claim 50 or 51, further comprising the step of attempting to identify a protein which correlates with said parent or precursor ions of interest.
53. A method as claimed in claim 52, further comprising determining which peptide products are predicted to be formed when a protein is digested and determining whether any predicted peptide product(s) correlate with parent or precursor ions of interest.
54. method as claimed in claim 52, further comprising determining whether said parent or precursor ions of interest correlate with one or more proteins.
55. A method as claimed in any preceding claim, wherein said first and second samples are taken from the same organism.
56. A method as claimed in any of claims 1-54, wherein said first and second samples are taken from different organisms.
57. A method as claimed in any preceding claim, further comprising the step of confirming that said first parent or precursor ions and/or said second parent or precursor ions are not fragment, product, daughter or adduct ions caused by fragmentation of parent or precursor ions in said collision, fragmentation or reaction device.

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58. A method as claimed in claim 57, further comprising: comparing a first mass spectrum relating to data obtained in said first mode with a second mass spectrum relating to data obtained in said second mode, said mass spectra being obtained at substantially the same time; and determining that said first and/or said second parent or precursor ions are not fragment, product, daughter or adduct ions if said first and/or said second parent or precursor ions have a greater intensity in the second mass spectrum relative to the first mass spectrum.
59. A method as claimed in any preceding claim, wherein parent or precursor ions from said first sample and parent or precursor ions from said second sample are passed to the same collision, fragmentation or reaction device.
60. A method as claimed in any of claims 1-58, wherein parent or precursor ions from said first sample and parent or precursor ions from said second sample are passed to different collision, fragmentation or reaction devices.
61. A mass spectrometer comprising: a Surface Induced Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon impinging upon a surface or target plate to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; -90 - (ii) determines the intensity of second parent or precursor ions from a second sample which have said same first mass to charge ratio; and (iii) compares the intensity of said first parent or precursor ions with the intensity of said second parent or precursor ions; wherein if the intensity of said first parent or precursor ions differs from the intensity of said second parent or precursor ions by more than a predetermined amount then either said first parent or precursor ions and/or said second parent_or precursor ions are considered to be parent or precursor ions-of interest.
62. A mass spectrometer comprising: a collision, fragmentaj or reaction device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in use: (1)-determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have said same first mass to charge ratio; and (iii) compares the intensity of said first parent or precursor ions with the intensity of second parent or precursor ions; wherein if said intensity of said first parent or precursor ions differs from said intensity of said second parent or precursor ions by more than a predetermined amount then either -91 -said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; wherein said collision, fragmentatj or reaction device selected from the group consisting of: (i) an Electron Collision or Impact Dissociation fragmentj device; (ii) a Photo Induced Dissociation ("PID") fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmentation device; (vii) an in-source fragmentation device; (Viii) an ion-source Collision Induced Dissociation fragmentajo device; (ix) a thermal or temperature source fragmentation device; (x) an electric field induced

fragmentaej device; (xi) a magnetic field induced

fragmenaj device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an iOn-jon reaction fragmentajo device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation device; (xvi) an ion-metastable ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an iOn-metastle atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxii) an iOn-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastab].e molecule reaction device for reacting ions to form adduct or product IOflS; and (xxiv) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.
63. A mass spectrometer comprising: -92 -a Surface Induced Dissociation fragmentation device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented upon impinging upon a surface or target plate to form fragment or daughter ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have said same first mass to charge ratio; (iii) determines a first ratio of the intensity of said first parent or precursor ions to the intensity of other parent or precursor ions in said first sample; (iv) determines a second ratio of the intensity of said second parent or precursor ions to the intensity of other parent or precursor ions in said second sample; and (v) compares said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are consjderj to be parent or precursor ions of interest.
64. A mass spectrometer comprising: a cOlliSiofl, fragmentation or reaction device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in use: Ci) determines the intensity of first parent or precursor ions from a first sample which have a first mass to charge ratio; (ii) determines the intensity of second parent or precursor ions from a second sample which have said same first mass to charge ratio; (iii) determines a first ratio of the intensity of said first parent or precursor ions to the intensity of other parent or precursor ions in said first sample; - (iv) determines a second ratio of the intensity of said second parent or precursor ions to the intensity of other parent or precursor ions in said second sample; and (v) compares said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are Considered to be parent or precursor ions of interest; wherein said collision, fragmenttj or reaction device selected from the group Consisting of: (1) an Electron Collision or Impact Dissociation fragmentation device; (ii) a Photo Induced Dissociation (P1D) fragmentation device; (iii) a Laser Induced Dissociation fragmentation device; (iv) an infrared radiation induced dissociation device; (v) an ultraviolet radiation induced dissociation device; (vi) a nozzle-skimmer interface fragmenttjo device; (vii) an in-source fragmentajo device; (Viii) an ion-source Collision Induced Dissociation fragmentajo device; (ix) a thermal or temperature source fragmentation device; Cx) an electric field induced fragmentation device; (xi) a magnetic field induced fragmentaj device; (xii) an enzyme digestion or enzyme degradation fragmentation device; (xiii) an ion-ion reaction fragmentation device; (xiv) an ion-molecule reaction fragmentation device; (xv) an ion-atom reaction fragmentation -94 -device; (xvi) an ion-metastable ion reaction fragmentation device; (xvii) an ion-metastable molecule reaction fragmentation device; (xviii) an ion-metastable atom reaction fragmentation device; (xix) an ion-ion reaction device for reacting ions to form adduct or product ions; (xx) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxi) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxii) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-metastable molecule reaction devico-. for reacting ions to form adduct or product ions; and (xxiv) an ion-metastab].e atom reaction device for reacting ions to form adduct or product ions.
65. A mass spectrometer as claimed in any of claims 61-64, further comprising an ion source.
66. A mass spectrometer as claimed in claim 65, wherein said ion Source is selected from the group consisting of: (i) an Electrospray lonisation (NESIa) ion source; (ii) an Atmospheric Pressure Photo lonisation ("APPI") ion source; (iii) an Atmospheric Pressure Chemical Ionisatjon ("APCI") ion Source; (iv) a Matrix Assisted Laser Desorption lonisation ("MALDI") ion source; Cv) a Laser Desorptjon Ionisatjon ("LDI') i'on source; (vi) an Atmospheric Pressure Ionjsatjon ("API") ion source; (vii) a Desorption Ionisatjon on Silicon ("DIOS') ion source; (viii) an Electron Impact ("El") ion source; (ix) a Chemical Ionjsatjon ("CI") ion source; Cx) a Field lonisation ("Fl") ion source; (xi) a Field Desorption ("FD") ion source; (xii) an Inductively Coupled Plasma ("ICP") ion source; (xiii) a Fast Atom Bombardment ("FAB") ion source; (xiv) a Liquid Secondary Ion Mass Spectrometry ("LSIMS") ion source; (xv-) a Desorption Electrospray Iónisatjon ("DESI") ion source; (xvi) a Nicicel-63 radioactive ion source; (xvii) an Atmospheric Pressure Matrix -95 -Assisted Laser Desorption Ionisatjon ion source; and (xviii) a Thermospray ion source.
67. A mass spectrometer as claimed in claim 65 or 66, wherein said ion Source comprises a pulsed or COntInUOUS ion Source.
68. A mass spectrometer as claimed in any of claims 65, 66 or 67, wherein said ion source is provided with an eluent over a period of time, said eluent having been separated from a mixture by means c.f liquid chromatography or capillary electrophoresis
69. A mass spectrometer as claimed in any of claims 65, 66 or 67, wherein said ion source is provided with an eluent over a -period of time, said eluent having been separated from a mixture by means of gas chromatography
70. A mass spectrometer as claimed.in any of claims 61-69, wherein said mass analyser is selected from the group consisting of: (i) a quadrupole mass analyser; (ii) a 2D or linear quadrupole mass analyser; (iii) a Paul or 3D quadrupole mass analyser; (iv) a Penning trap mass analyser; (v) an ion trap mass analyser; (vi) a magnetic sector mass analyser; (vii) Ion Cyclotron Resonance (IICRU) mass analyser; (viii) a Fourier Transform Ion Cyclotron Resonance (FTICR) mass analyser; (ix) an electrostatic or orbitrap mass analyser; (x) a Fourier Transform electrostatic or orbitrap mass analyser; and (xi) a Fourier Transform mass analyser; (Xii) a Time of Flight mass analyser; (xiii) an orthogonal acceleration Time of Flight mass analyser; (xiv) an axial acceleration Time of Flight mass analyser; and (xv) a quadrupole rod set mass filter or mass analyser.
71. A mass spectrometer as claimed in any of claims 61-70, further comprising an ion trap or ion guide arranged upstream -96 -and/or downstream of said collision, fragmentation or reaction device.
72. A mass spectrometer as claimed in claim 71, wherein said ion trap or ion guide is selected from the group consisting of: (i) a multjpo].e rod set or a segmented multipole rod set ion trap or ion guide comprising a quadrupo].e rod set, a hexapole rod set, an octapole rod set or a rod set comprising more than eight rods; (ii) an ion tunnel or ion funnel ion trap or ion ide comprising a plurality of electrodes or at least 2, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 electrodes having apertures through which ions are transmitted in use, wherein at least 5%, - 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of said electrodes have apertures which are of substantially the same size or area or which have apertures which become progressively larger and/or smaller in size or in area; (iii) a stack or array of planar, plate or mesh electrodes, wherein said stack or array of planar, plate or mesh electrodes comprises a plurality or at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 planar, plate or mesh electrodes and wherein at least 5%, 10%, 15%, 20%, 25%, 30%, 35, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of said planar, plate or mesh electrodes are arranged generally in the plane in which ions travel in use; and (iv) an ion trap or ion guide comprising a plurality of groups of electrodes arranged axially along the length of the ion trap or ion guide, wherein each group of electrodes comprises: (a) a first and a second electrode and means for applying a DC voltage or potential to said first and second electrodes in order to confine ions in a first radial direction within said ion guide; and (b) a third and a fourth electrode and means for applying an AC or RF voltage to said third and -97 -fourth electrodes in order to confine ions in a second radial direction within said ion guide.
73. A mass spectrometer as claimed in claim 72, wherein said ion trap or ion guide comprises an ion tunnel or ion funnel ion trap or ion guide wherein at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of said electrodes have internal diameters or dimensions selected from the group consisting of: Ci) �= 1.0 mm; (ii) �= 2.0 mm; (iii) �= 3.0 mm; (iv) �= 4.0.mm; (v) �=5.O mm; (vi) �= 6.0 nun; (vii) �= 7.0 nun; (Viii) �= 8.0 mm; (ix) �= 9.0 mm; (x) �= 10.0 nun; and (xi) > 10.0 nun.
74. A mass spectrometer as claimed in claim 71, 72 or 73, wherein said ion trap or ion guide further comprises first AC or RF voltage means arranged and adapted to apply an AC or RF voltge to at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of said plurality of electrodes of said ion trap or ion guide in order to confine ions radially within said ion trap or ion guide.
75. A mass spectrometer as claimed in claim 74, wherein said first Ac or RF voltage means is arranged and adapted to apply an AC or RF voltage having an amplitude selected ftom the group cOnsisting of: (1) < 50 V peak to peak; (ii) 50-100 V peak to peak; (iii) 100-150 V peak to peak; (iv) 150-200 V peak to peak; (v) 200-250 V peak to peak; (vi) 250-300 V peak to peak; (vii) 300-350 V peak to peak; (viii) 350-400 V peak to peak; (ix) 400- 450 V peak to peak; (x) 450-500 V peak to peak; and (xi) > 500 V peak to peak.
76. A mass analyser as claimed in claim 74 or 75, wherein said first AC or RF voltage means is arranged and adapted to apply an AC or RF voltage having a frequency selected from the group -98 -Consisting of: (i) < 100 kHz; (ii) 100-200 kHz; (iii) 200-300 kllz; (iv) 300-400 kffz; (v) 400-500 kHz; (vi) 0.5-1.0 MHz; (Vii) 1.0-1.5 MHz; (viii) 1.5-2.0 MHz; (ix) 2.0-2.5 MHz; (x) 2.5-3.0 MHZ; (xi) 3.0-3.5 MHz; (xii) 3.5-4.0 MHz; (xiii) 4.0-4.5 MHz; (xiv) 4.5-5.0 MHz; (xv') 5.0-5.5 MHz; (xvi) 5.5-6.0 MHz; (xvii) 6.0-6.5 MHz; (xviii) 6.5-7.0 MHz; (xix) 7.0-7.5 MHz; (xx) 7.5- 8.0 MHz; (xxi) 8.0-8.5 MHz; (xxii) 8.5-9.0 MHz; (xxiii) 9.0-9.5 MHz; (xxiv) 9.5-10.0 MHz; arid (xxv) > 10.0 MHz.
77. A moss sDectrometer as claimed in any of claims 71-76, wherein said ion trap or ion guide is arranged and adapted to receive a beam or group of ions and to convert or partition said beam or group of ions such that a plurality or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 separate packets of ions are confined and/or isolated in said ion trap or ion guide at any particular time, and wherein each packet of ions is separately confined and/or isolated in a separate axial potential well formed within said ion trap or ion guide.
78. A mass spectrometer as claimed in any of claims 71-77, further comprising means arranged and adapted to urge at least some ions upstream and/or downstream through or along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial length of said ion trap or ion guide in a mode of operation.
79. A mass spectrometer as claimed in any of claims 71-78, further comprising first transient DC voltage means arranged and adapted to apply one or more transient DC voltages or potentials or one or more transient DC voltage or potential waveforms to said electrodes forming said ion trap or ion guide in order to urge at least some ions upstream and/or downstream along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, -99 - 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial length of said ion trap or ion guide.
80. A mass spectrometer as claimed in any of claims 71-79, further comprising AC or RF voltage means arranged and adapted to apply two or more phase-shjf ted AC or RF voltages to electrodes forming said ion trap or ion guide in order to urge at least some ions upstream and/or downstream along at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the axial lengthof said ion *;.*L;*., trap or ion guide.
81. A mass spectrometer as claimed in any of claims 71-80, further comprising means arranged and adapted in a mode of operation to maintain at least a portion of said ion trap or ion guide at a pressure selected from the group consisting of: (i) > 0.0001 mbar; (ii) > 0.001 mbar; (iii) > 0.01 mbar; (iv) > 0.1 mbar; (v) > 1 mbar; (vi) > 10 mbar; (vii) > 1 mbar; (Viii) 0.0001-100 mbar; and (ix) 0.001-10 mbar.
82. A mass spectrometer as claimed in any of claims 61-81, further comprising a mass filter arranged upstream and/or downstream of said collision, fragmentation or reaction device.
83. A mass spectrometer as claimed in any of claims 61-82, wherein said collision, fragmentation or reaction device comprises: (I) a quadrupole rod set; (ii) an hexapole rod set; (iii) an octopole or higher order rod set; (iv) an ion tunnel comprising a plurality of electrodes having apertures through which ions are transmitted; or (v) a plurality of electrodes connected to an AC or RF voltage supply for radially confining ions within said collision, fragmentation or reaction device.
84. A mass spectrometer as claimed in any of claims 61-83, wherein said collision, fragmentation or reaction device forms a -100 -Substantially gas-tight enclosure apart from an aperture t admit ions and an aperture for ions to exit from and optionally a port for introducing gas.
85. A mass spectrometer as claimed in any of claims 61-84, wherein said collision, fragmentaj or reaction device is maintained at a pressure selected from the group Consisting of: (i) greater than or equal to 0.000]. inbar; (ii) greater than or equal to 0.0005 mbar; (iii) greater than or equal to 0.001 mbar; (iv) greater than or equal to 0.005 mbar; (v-greater than or

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equal to 0.01 mbar; (vi) greater than or equal to 0.05 rnbar; (Vii) greater than or equal to 0.1 inbar; (viii) greater than or equal to 0.5 mbar; (ix) greater than or equal to 1 mbar; Cx) greater than or equal to 5 mbar; and (xi) greater than or equal to 10 rnbar.
86. A mass spectrometer as claimed in any of claims 61-85, wherein said collision, fragmentaj or reaction device is maintained at a pressure selected from the group Consisting of: (ii less than or equal to 10 mbar; (ii) less than or equal to 5 mbar; (iii) less than or equal to 1 mbar; (iv) less than or equal to 0.5 mbar; (v) less than or equal to 0.1 rnbar; (vi) less than or equal to 0.05 mbar; (vii) less than or equal to 0.01 mbar; (viii) less than or equal to 0.005 inbar; (ix) less tharr'or equal to 0.001 nthar; Cx) less than or equal to 0.0005 inbar; and (xi) less than or equal to 0.0001 mbar.
87. A mass spectrometer as claimed in any of claims 61-86, wherein gas in said collision, fragmentaj or reaction device is maintained at a first pressure when said collision, fragmentaj or reaction device is in said first mode and at a second lower pressure when said collision, fragmentation or reaction device is in said second mode.

-101 -
88. A mass spectrometer as claimed in any of claims 61-87, wherein gas in said collision, fragmentation or reaction device comprises a first gas or a first mixture of gases when said collision, fragmentation or reaction device is in said first mode and a second different gas or a second different mixture of gases when said collision, fragmentation or reaction device is in said second mode.
89. A mass spectrometer as claimed in any of claims 61-88, wherein parent or precursor ions from said first sample and parent or precursor-ions from said second sample are passed to the same collision, fragmentation or reaction device.
90. A mass spectrometer as claimed in any of claims 61-89, wherein parent or precursor ions from said first sample and parent or precursor ions from said second sample are passed to different collision, fragmentation or reaction devices.
91. A mass spectrometer as claimed in any of claims 61-90, wherein molecules from said first and/or second samples are separated from a mixture of other molecules prior to being ionised by-: (i) High Performance Liquid Chromatography (HPL,C'); (ii) anion exchange; (iii) anion exchange chromatography; (iv) cation exchange; Cv) cation exchangechromatography; (vi) ion pair reversed-phase Chromatography; (vii) chromatography; (viii) single dimensional electrophoresjs; (ix) multi-dimensional electrophoresis; (x) size exclusion; (xi) affinity; (xii) reverse phase chromatography; (Xiii) Capillary Electrophoresjs Chromatography (NCEC); (xiv) electrophoresis; (xv) ion mobility separation; (xvi) Field Asymmetric Ion Mobility Separation (FAIMS'); or (xvi) capillary electrophoresis.
92. A method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a collision, fragmentation or reaction device; -102 -repeatedly switching, altering or varying said collision, fragmentation or reactio n device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a collision, fragmentation or reaction device; repeatedly switching, altering or varying said collision, -.

-. fragmentation or reaction device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from said first sample, said first fragment, product, daughter or adduct ions having a first mass to charge ratio; automatically determining the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from said second sample, said second fragment, product, daughter or adduct ions having said same first mass to charge ratio; and comparing the intensity of said first fragment, product, daughter or adduct ions with the intensity of said second fragment, product, daughter or adduct ions; wherein if the intensity of said first fragment, product, daughter or adduct ions differs from the intensity of said second fragment, product, daughter or adduct ions by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; and wherein said collision, fragmentajon or reaction device is selected from the group Consisting of: (1) a Surface Induced Dissociation (S1D") fragmentatjo device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Collision or Impact Dissociation fragmentation device; (iv) a Photo Induced Dissociation ("PID) fragmentation device; (v) a Laser Induced Dissociation fragmentation device; (vi) an infrared radiation induced dissociation device; (vii) an ultraviolet radiation induced dissociation device; (viii) a nozz1e-skjer interface fragmentation device; (ix) an in-source fragmentaj device; (x) an ion-source Collision Induced Dissociation fragmentation device; (xi) a thermal or temperature source fragmentation device; (xii) an electric field induced fragmentation device; (xiii) a magnetic field induced fragmentaj device; (xiv) an enzyme digestion or enzyme degradation fragmentation device; (xv) an ion-ion reaction fragmentation device; (xvi) an ion-molecule reaction fragmentation device; (xvii) an ion-atom reaction fragmentation device; (xviii) an ion-metastable ion reaction fragmentation device; (xix) an iOfl-metastable molecule reaction fragmentation device; (xx) an ion-metastable atom reaction fragmentation device; (xxi) an ion-jon reaction device for reacting ions to form adduct or product ions; (xxii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (Xxv) an ion-metastable molecule reaction device for reacting ions to form adduct or product Ofl$; and (xxvi) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.
93. A method of mass spectrometry comprising: passing parent or precursor ions from a first sample to a Collision, fragmentation or reaction device; -104 -repeatedly switching, altering or varying said collision, fragmentation or reaction device between a first mode wherein at least some of said parent or precursor ions from said first sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; passing parent or precursor ions from a second sample to a Collision, fragmentation or reaction device; repeatedly -switching, altering or varying said collision, fragmenttj or reaction device between a first mode wherein at least some of said parent or precursor ions from said second sample are fragmented or reacted into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; automatically determining the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from said first sample, said first fragment, product, daughter or adduct ions having a first mass to charge ratio; automatically determining the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from said second sample, said second fragment, product, daughter or adduct ions having said same first mass to charge ratio; determining a first ratio of the intensity of said first fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in said first sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in said first sample; determining a second ratio of the ittensity of said second fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in said second sample or with the -105 -intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in said second sample; comparing said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; and wherein said Colljsio, fragmentajn or reaction device-is selected from the group Consisting of: (I) a Surface Induced Dissociation (SIDe) fragmentation device; (ii) an Electron Transfer Dissociation fragmentao device; (ill) an Electron Collision or tmpact Dissociation fragmentation device; (iv) a Photo Induced Dissociation (PID") fragmentation device; (v) a Laser Induced Dissociation fragmentation device; (vi) an infrared radiation induced dissociation device; (vii) an ultraviolet radiation induced dissociation device; (viii) a nozzle-skjner interface fragmentation device; (ix) an in-source fragmentation device; (x) an ion-source Collision Induced Dissociation fragmentajo device; (xi) a thermal or temperature source fragmenaj device; (xii) an electric field induced fragmentation device; (xiii) a magnetic field induced fragmentaj device; (xiv) an enzyme digestion or enzyme degradatjo fragmentajo device; (xv) an ion-ion reaction fragmentajo device; (xvi) an ion-molecule reaction fragmentajo device; (xvii) an ion-atom reaction fragmentatjo device; (xviii) an ion-metastable ion reaction fragmentation device; (Xix) an ion-metastle molecule reaction fragmentation device; (xx) an ion-metastable atom reaction fragmentatjo device; (xxi) an iOfl-j0 reaction device for reacting ions to form adduct or product ions; (xxii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-metastable ion reaction device for -106 - reacting ions to form adduct or product iOns; (Xxv) an ion-metastable molecule reaction device for reacting ions to form adduct or product ions; and (xxvi) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.
94. A mass spectrometer comprising: a collision, fragmentaj or reaction device which is arranged and adapted to be repeatedly switched, altered or varied in use between a first mode wherein at least some parent or precursor ions are fragmented or reacted into one or more fragment1 product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented or reacted; a mass analyser; and a control system which in use: (i) determines the intensity of first fragment, product, daughter or adduct IOflS derived from first parent or precursor ions from a first sample, said first fragment, product, daughter or adduct ions having a first mass to charge ratio; (ii) determines the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from a second sample, said second fragment, product, daughter or adduct ions having said same first mass tocharge ratio; and (iii) compares the intensity of said first fragment, product, daughter or adduct ions with the intensity of said second fragment, product, daughter or adduct ions; wherein if the intensity of said first fragment, product, daughter or adduct ions differs from the intensity of said second fragment, product, daughter or adduct ions by more than a predetermined amoujt then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; and -107 -wherein said collision, fragmentation or reaction device is selected from the group consisting of: (i) a Surface Induced Dissociation (SID') fragmentation device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Collision or Impact Dissociation fragmentation device; (iv) a Photo Induced Dissociation (PID") fragmentation device; (v) a Laser Induced Dissociation fragmentation device; (vi) an infrared radiation induced dissociation device; (vii) an ultraviolet radiation induced dissociation device; (viii) a nozzle-skimme.interface fragmentation device; (ix) an in-source fragmentation device; (x) an ion-source Collision Induced Dissociation fragmentation device; (xi) a thermal or temperature source fragmentation device; (xii) an electric field induced fragmentation device; (xiii) a magnetic field induced fragmentation device; (xiv) an enzyme digestion or enzyme degradation fragmentation device; (xv) an ion-ion reaction fragmentation device; (xvi) an ion-molecule reaction fragmentation device; (xvii) an ion-atom reaction fragmentation device; (xviii) an ion-nietastab].e ion reaction fragmentation device; (xix) an ion-metastable molecule reaction fragmentation device; (xx) an ion-metastab].e atom reaction fragmentation device; (xxi) an ion-ion reaction device for reacting ions to form adduct or product ions; (xxii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-metastable ion reaction device for reacting ions to form adduct or product ions; (xxv) an ion-metastable molecule reaction device for reacting ions to form adduce or product ions; and (xxvi) an ion-zuetastable atom reaction device for reacting ions to form adduct or product ions.
95. A mass spectrometer comprising: a collision, fragmentation or reaction device repeatedly switched, altered or varied in use between a first mode. wherein -108 -at least some parent or precursor ions are fragmented into one or more fragment, product, daughter or adduct ions and a second mode wherein substantially fewer parent or precursor ions are fragmented; a mass analyser; and a control system which in use: (i) determines the intensity of first fragment, product, daughter or adduct ions derived from first parent or precursor ions from a first sample, said first fragment, product, daughter or adduct ions having a first mass to charge ratio; - (ii) determines the intensity of second fragment, product, daughter or adduct ions derived from second parent or precursor ions from a second sample, said second fragment, product, daughter or adduct ions having said same first mass to charge ratio; (iii) determines a first ratio of the intensity of said first fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in said first sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in said first sample; (iv) determines a second ratio of the intensIty of said second fragment, product, daughter or adduct ions to the intensity of other parent or precursor ions in said second 25, sample or with the intensity of other fragment, product, daughter or adduct ions derived from other parent or precursor ions in said second sample; and Cv) compares said first ratio with said second ratio; wherein if said first ratio differs from said second ratio by more than a predetermined amount then either said first parent or precursor ions and/or said second parent or precursor ions are considered to be parent or precursor ions of interest; and wherein said Collision, fragmentation or reaction device is selected from the group consisting of: (i) a Surface Induced -109 -Dissociation (NSIDN) fragmentation device; (ii) an Electron Transfer Dissociation fragmentation device; (iii) an Electron Collision or Impact Dissociation fragmentation device; (iv) a Photo Induced Dissociation (TMPID") fragmentation device; Cv) a Laser Induced Dissociation fragmentation device; (vi) an infrared radiation induced dissociation device; (vii) an ultraviolet radiation induced dissociation device; (viii) a nozzle-skier interface fragmentation device; (ix) an in-source fragmentation device; Cx) an ion-source Collision Induced Dissociation fragmentation device; (xi) a thermal or temperature source fragmentation device; (xii) an electric field induced fragmentation device; (xiii) a magnetic field induced fragmentation device; (xiv) an enzyme digestion or enzyme degradation fragmentation device; (xv) an ion-ion reaction fragmentation device; (xvi) an ion-molecule reaction fragmentation device; (xvii) an ion-atom reaction fragmentation device; (xviii) an ion-metastable ion reaction fragmentation device; (xix) an ion-metastaj1e molecule reaction fragmentation device; (xx) an ion-inetastable atom reaction fragmentation device; (xxi) an ion-jon reaction device for reacting ions to form adduct or product ions; (xxii) an ion-molecule reaction device for reacting ions to form adduct or product ions; (xxiii) an ion-atom reaction device for reacting ions to form adduct or product ions; (xxiv) an ion-metastable ion reaction device for reacting ions to form adduct or product.ions; (xxv) an ion- xnetastable molecule reaction device for reacting ions to form adduct or product ions; and (xxvi) an ion-metastable atom reaction device for reacting ions to form adduct or product ions.