J. Throck Watson, O. David Sparkman

Introduction to Mass Spectrometry

Instrumentation, Applications and Strategies for Data Interpretation

• Gebundenes Buch

Produktbeschreibung

Completely revised and updated, this text provides an easy-to-read guide to the concept of mass spectrometry and demonstrates its potential and limitations. Written by internationally recognised experts and utilising "real life" examples of analyses and applications, the book presents real cases of qualitative and quantitative applications of mass spectrometry. Unlike other mass spectrometry texts, this comprehensive reference provides systematic descriptions of the various types of mass analysers and ionisation, along with corresponding strategies for interpretation of data. The book concludes with a comprehensive 3000 references.This multi-disciplined text covers the fundamentals as well as recent advance in this topic, providing need-to-know information for researchers in many disciplines including pharmaceutical, environmental and biomedical analysis who are utilizing mass spectrometry

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Produktdetails

• Verlag: Wiley & Sons
• Artikelnr. des Verlages: 14551634000
• 4. Aufl.
• Seitenzahl: 848
• Erscheinungstermin: 1. November 2007
• Englisch
• Abmessung: 261mm x 202mm x 53mm
• Gewicht: 1790g
• ISBN-13: 9780470516348
• ISBN-10: 0470516348
• Artikelnr.: 22947397

Autorenporträt

J. Throck Watson is professor of chemistry and biochemistry at Michigan State University. He received his B.S. in 1961from Iowa State University and his PhD in 1965 from MIT. From 1965 - 68 he was a postdoctoral Researcher at the University of Strasbourg from which he transferred in 1969 to the University of Vanderbilt's Department of Pharmacology. In 1980 he was appointed Professor of Biochemistry and Chemistry at Michigan State University as well as Director of the J.T. Watson Mass Spectrometry Facility. In 1990 he was awarded the Pittsburgh Spectroscopy Society Award. He has published over 150 scientific papers, 15 book chapters and 4 books. He currently serves on the editorial board of Mass Spectrometry Reviews and Current Analytical Chemistry. He retired from MSU in August 2006 to complete the writing of this book. O. David Sparkman is currently an Adjunct Professor of Chemistry at the University of the Pacific in Stockton, California; a Consultant to the National Institute of Standards and Technology Mass Spectrometry Data Center. He teaches courses in mass spectrometry and analytical chemistry and manages the mass spectrometry facility. Over the past 30 years, he has developed and taught five different ACS courses in mass spectrometry; he holds positions on the Editorial Advisory Boards of the European Journal of Mass Spectrometry. He is the author of Mass Spectrometry Desk Reference. He has developed and taught 10 sessions of an interactive Web Course on Mass Spectral Interpretation over the past 4 years. David Sparkman has been a member of ASMS since 1977 and the ACS since 1967. He is a former member of the ACS Continuing Education Committee. He was the invited teacher of the Mass Spectral Interpretation course held at the 17th International Mass Spectrometry Conference held in Prague, the Czech Republic, in August of 2006.

Inhaltsangabe

Chapter 1: Introduction.
I. What is Mass Spectrometry.
II. History.
III. Applications.
IV. The Data of Mass Spectrometry and Its Presentation.
1. Spectra.
2. Total Ion Current.
3. Mass Chromatograms and Profiles.
V. Definition of Terms.
1. Mass-To-Charge Ratio (m/z).
2. Multiple-Charge Ions.
3. Ions Representing an Intact Molecule.
4. Resolution/Resolving Power.
5. Intensity vs Abundance.
Chapter 2: The Mass Spectrometer.
I. Introduction.
II. Ion Guides.
III. Types of m/z Analyzers.
1. Time-Of-Flight.
A. Linear.
1) Resolving Power of the Linear TOF Instrument.
2) Time-Lag Focusing.
3) Beam Deflection.
B. Reflectron.
C. Orthogonal Acceleration.
D. Ion Detection in the TOF Analyzer.
1) Time Slice Detection.
2) Time Array Detection.
3) TAD with Transient Recorders.
4) TAD with an Integrating Transient Recorder.
5) Hadamard Transform TOF MS.
2. Quadrupole Ion Traps.
A. 3D Quadrupole Ion Traps.
B. Linear Quadrupole Ion Traps.
3. Orbitrap.
A. Historical Aspects.
B. Operating Principles.
4. Transmission Quadrupoles.
A. QMF Equations of Motion.
B. The Stability Diagram.
C. Characteristics of Output.
D. Spectral Skewing.
E. Performance Limitations.
5. Sector instruments.
A. Single-focusing Instruments.
1) Operating Principles.
2) Performance Limitations.
B. Double-Focusing Instruments.
6. FTICR-MS.
C. Hardware Configuration.
D. Operational Considerations.
E. Representative Applications.
IV. Calibration of the m/z Scale.
1. Electron Ionizaton (GC/MS).
2. Chemical Ionization (GC/MS).
3. Electrospray and Other Atmospheric Pressure Ionization Techniques.
V. Ion Detection.
1. General Considerations.
2. Types of Detectors.
A. Faraday Cup.
B. Electron Multiplier.
1) Discrete-Dynode Version.
2) Continuous-Dynode Version.
C. Negative-Ion Detection.
D. Post-Acceleration Detection and Detection of High-Mass Ions.
E. Channel Electron Multiplier Array (CEMA).
F. Electro-Optical Ion Detection.
G. The Daly Detector.
H. Cryogenic Detectors.
VI. Vacuum Systems.
1. Introduction.
2. Definitions.
3. Pressure Gauges.
A. Thermal-Conductivity Gauges.
B. Ionization Gauges.
4. Types of Pumps.
A. Mechanical Pumps (Low Vacuum).
1) Rotary Vane.
2) Scroll.
3) Diaphram.
B. High Vacuum.
1) Turbomolecular Pumps.
2) Diffusion Pumps.
3) Sputter-Ion Pumps.
4) Cryogenic Pumps.
Chapter 3: Mass Spectrometry/Mass Spectrometry.
I. Introduction.
1. Concept and Definitions.
2. Nomenclature.
II. Ion Dissociation.
1. Metastable Ions.
III. Instrumentation for MS/MS.
1. MS/MS in Space.
A. Tandem MS/MS.
1) Triple-Quadrupole Mass Spectrometer.
2) BEqQ Hybrid Instrument.
B. Double-Focusing Instruments.
2. MS/MS in Time.
IV. Specialized Techniques and Applications.
1. In-Source CAD.
2. CAD in Conjunction with Soft Ionization.
3. Selected Reaction Monitoring.
4. Precursor-Ion Scan.
5. Neutral Loss (Common Loss) Scan.
6. Ion/Molecule Reactions.
V. Identification of Unknowns from CAD Data.
1. Accurate Mass Measurements.
2. Library Search Utilities.
A. Other Databases.
B. Substructure Information.
C. Use of MS Interpreter.
Chapter 4: Inlet Systems.
I. Introduction.
II. Batch Inlets.
1. Heated Reservoir Inlet.
2. Direct Inlet Probe (DIP).
A. The Chromatoprobe.
3. Direct Exposure Probe (Desorption Chemical Ionization [DCI]).
4. Pyrolysis.
III. Continuous Inlets.
1. Membrane Introduction MS (MIMS).
2. Supercritical Fluid Chromatography.
3. Electrophoretic Inlet.
IV. Ionization Inlet Systems.
1. Direct Analysis in Real Time (DART).
2. Desorption Electrospray Ionization (DESI).
3. Desorption Atmospheric Pressure Chemical Ionization (DAPCI).
V. 4. Speciality Interfaces.
1. Selected Ion Flow-Tube Mass Spectrometry (SIFT-MS).
2. Fast Atom Bombardment (FAB) and Liquid Secondary Ion Mass Spectrometry
(LSIMS).
3. Chemical Reaction Interface Mass Spectrometry (CRIMS).
4. ICP.
Chapter 5: Strategies for Data Interpretation (Other than Fragmentation).
I. Introduction.
II. Some Important Definitions.
III. The Possible Information That Can be Obtained from the Mass Spectrum.
IV. Elemental Composition of an Ion and the Ratios of Its Isotope Peaks.
1. Definition of Terms Related to the Matter of Mass Spectrometry.
2. Nitrogen Rule.
3. Elemental Composition of an Ion Based on Intensities of Isotope Peaks.
B. Use of Isotope Peaks Intensities to Determine the Elemental Composition
of Ions.
C. Isotope Peaks Patterns for Ions Containing Various Combinations of Cl
and/or Br.
D. Constraints on the Number of Atoms of a Given Element.
E. Relationship between the Spacing of Isotope Peaks and the Charge State
of an Ion.
3) Ions of Low-Charge State.
4) Ions of High-Charge State.
F. Steps to Assigning an Elemental Composition Based on Isotope Peaks
Intensities.
G. Validating the Putative Elemental Composition of an Ion.
H. Some Illustrative Examples.
I. Potential Problems Arising from Adjacent Peaks.
4. Accurate Mass Measurements.
A. Appearance of Mass Spectra of High-m/z Value Ions.
5. Use of the NIST Mass Spectral Search Program in the Determination of a
Structure from an Elemental Composition.
6. Does the Result Make Sense?
V. Identifying the Molecular Mass of an Analyte.
1. Identification of a Molecular-Ion Peak.
2. Identification of a Protonated-Molecule Peak.
A. The Role of Adduct-Ion Peaks.
3. Recognition of the Deprotonated Molecule ([M - H] - ) Peak in Soft
Ionization.
VI. Recognition of Spurious Peaks in the Mass Spectrum.
1. Noise Spikes.
2. Peaks Corresponding to Contaminants in GC/MS and LC/MS.
A. Phthalate Ion.
B. GC Column Bleed.
C. Solvent Clusters.
VII. Obtaining Structural Information from Mass Spectra.
Chapter 6: Electron Ionization.
I. Introduction.
II. Ionization Process.
III. Strategy for Data Interpretation.
1. Assumptions.
2. The Ionization Process.
IV. Types of Fragmentation Pathways.
1. Sigma-Bond Cleavage.
2. Homolytic Cleavage.
3. Heterolytic Cleavage.
4. Rearrangements.
A. Hydrogen Shift Rearrangements.
B. Hydride Shift Rearrangements.
V. Representative Fragmentations (Spectra) of Classes of Compound.
1. Hydrocarbons.
A. Saturated Hydrocarbons.
1) Straight Chain.
2) Branched.
3) Cyclic.
B. Unsaturated.
C. Aromatic.
2. Alkyl Halides.
3. Oxygen-Containing Compounds.
A. Aliphatic Alcohols.
B. Aliphatic Ethers.
C. Aromatic Alcohol.
D. Cylic Ethers.
E. Ketones and Aldehydes.
F. Esters and Acids.
1) Aliphatic.
2) Aromatic.
4. Nitrogen-Containing Compounds.
A. Aliphatic Amines.
B. Aromatic Compounds with Nitrogen Atoms.
C. Heterocyclic Nitrogen Compounds.
D. Nitro Compound.
E. Concluding Remarks on Nitrogen Containing Compounds.
5. Multiple Heteroatoms or Heteroatoms and Double Bonds.
6. Trimethylsilyl Derivatives.
7. Determining the Location of Double Bonds.
VI. Library Search.
1. Databases.
2. Library Search Programs.
3. What to Do When the Spectrum of the Unknown Is Not In the Database(s).
4. Searching Multiple Databases.
5. Database Size and Quality.
6. Concluding Remarks on the NIST Mass Spectral Search Program.
VII. Summary of Interpretation of EI Mass Spectra.
Chapter 7: Chemical Ionization.
I. Introduction.
II. Description of the Chemical Ionization Source.
III. Production of Reagent Ions from Various Reagent Gases.
IV. Positive-Ion Formation Under CI.
1. Fundamentals.
2. Practical Consideration of Proton Affinity.
3. Selective Ionization.
4. Fragmentation.
V. Negative-Ion Formation under CI.
VI. Data Interpretation and Systematic Studies of CI.
VII. Ionization by Charge Exchange.
1. Mechanism of Ionization.
2. Fragmentation and Appearance of Mass Spectra.
IX. Desorption Chemical Ionization .
X. General Applications.
Chapter 8: Electrospray Ionization.
I. Introduction.
II. Operating Principles.
III. Appearance of ESI Mass Spectra and Data Interpretation.
IV. ESI with High Mass Resolving Power.
V. Implementations of Electrospray.
1. Conventional ESI Source Interface.
2. Nanospray and Microspray.
3. Desorption Electrospray Ionization (DESI).
VI. Effect of Composition and Flowrate of Analyte Solution.
VII. Special Applications.
1. Direct Analysis of Ions in Solution by ESI.
2. Cold Spray Ionization.
3. Negative Ion Detection.
4. Secondary Electrospray Ionization.
5. Kinetic Measurements of Chemical Reactions.
VIII. General Applications.
Chapter 9: MALDI.
I. Historical Perspective and Introduction.
II. Operating Principles.
1. The Matrix.
2. The Laser and m/z Analyzer.
3. The Ionization Process.
4. Atmospheric-Pressure MALDI.
III. Sample Handling.
1. Sample Preparation of the Conventional Plate.
2. The Problem of Analyte Solubility.
3. The Problem of Sample Purity.
4. On-Probe Sample-Cleaning Techniques.
A. SAMs and Polymer-Modified Surfaces
B. Affinity Surfaces.
5. Direct Analysis from Gels.
6. Hydrogen/Deuterium Exchange.
IV. Special Instrumental Techniques.
1. Post-Source Decay (PSD).
2. Ion Excitation.
3. Delayed Extraction (DE).
4. Desorption Ionization On Silicon (DIOS).
5. Tissue Profiling.
V. Representative Applications.
1. Peptides and Proteins.
2. Microbes.
3. Biomarkers.
4. Synthetic Polymers.
5. Small Molecules.
6. Quantitation.
7. Combined with Liquid Chromatography.
Chapter 10: GC/MS.
Introduction.
I. Introduction to GC.
1. Basic Types of Injection.
2. Injection Considerations and Syringe Handling.
II. Sample Handling.
III. Instrument Requirements for GC/MS.
1. Operating Pressures.
2. Typical Parameters for a GC-MS Interface.
3. Open-Split Interface.
4. Separators.
C. Jet-Orifice Separator.
D. Membrane Separator.
5. Inertness of Materials in the Interface.
6. Background/Bleed.
7. Qualitative vs Quantitative Assessment of GC/MS Data.
IV. Operational Considerations.
1. Spectral Skewing.
2. Rapid Scanning.
3. Fast Chromatography.
A. Status Quo.
B. Performance Trade-Offs of Conventional Instruments for GC/MS.
C. Time Array Detection.
4. Selected Ion Monitoring (SIM).
A. Definitions/Nomenclature.
B. Development of the Technique.
C. Introductory Qualitative Example.
D. Introductory Quantitative Example.
E. Mechanics of Ion Monitoring.
F. Programmable SIM.
G. SIM at High Resolving Power.
V. Sources of Error.
VI. Representative Applications of GC/MS.
Chapter 11: Liquid Chromatography/Mass Spectrometry.
I. Introduction.
II. Historical Milestones in the Development of the Interface.
1. Direct Inlet.
2. Moving Belt Interface.
3. Thermospray Interface.
4. Continuous Flow FAB.
III. Currently Viable Versions of the Interface.
1. Atmospheric-Pressure Ionization.
A. Electrospray Interface.
1 Optimization for Analyses by HPLC.
2) Data-Dependent Analysis.
3) Capillary Electrophoresis.
B. APCI.
C. APPI.
2. Particle Beam Interface.
3. EI.
IV. Operational Considerations (Special Operation of LC under MS
Conditions).
1. Solvents .
2. Buffers.
3. Columns.
4. etc.
V. Applications.
Chapter 12: Analysis of Proteins and other Biopolymers.
I. Proteins.
1. Sequencing.
A. Nomenclature and Fragmentation in Sequencing of Peptides.
B. Strategy for Deducing Amino Acid Sequence via CAD of Peptides.
1) An Illustrative Example.
2) Possible Pitfalls in Interpretation.
3) Search for Confirming Ions.
4) Ladder Sequencing.
2. Mass Mapping.
3. Posttranslational Modifications.
A. Phosphorylation.
1) An Illustrative Example.
2) Selective Capture and Detection of Phosphopeptides.
3) Chemical Modification of Phosphorylation Sites.
B. Recognition of Sites of Sulfation.
C. Recognition of Sites of Glycosylation.
D. Acetylation of Lysine.
E. Cysteine Status.
1) Are There Any Disulfide Bonds?
2) Which Cysteines Are Free?
3) What is the Linkage of Cysteines in Disulfide Bonds?
(a) Conventional Proteolytic Mass Mapping of Disulfides.
(b) Cyanlation-Based Mass Mapping of Disulfides.
4) Recognition of Ubiquinated Proteins.
4. Quantitation in Proteomics.
A. ICATs.
5) Operating Principles.
6) Illustrative Example of the ICAT Approach.
7) Analogous Developing Methodologies.
B. Alternative Stable-Isotope Labeling Methodology.
5. "Top-Down" Strategies of Analysis.
1) Instrumentation and Fragmentation Requirements.
2) Electron Capture Dissociation (ECD).
3) Electron Transfer Dissociation (ETD).
6. Non-Covalent Interactions.
7. Folding and Unfolding.
8. Applications.
II. Oligonucleotides.
1. Analytical Considerations.
2. Sequencing.
A. Nomenclature.
B. Algorithm for Data Interpretation.
3. Applications.
III. Carbohydrates.
1. Analytical Considerations.
2. Nomenclature.
3. Diagnostic Fragmentation.
4. Applications.