Overall efficiency and speed of analysis – key factors are ions per sample molecule desorbed and ions produced per laser pulse Precision and accuracy of.

Slides:



Advertisements
Similar presentations
MASS SPECTROMETRY AP Chemistry Big Idea 1
Advertisements

High Performance MALDI MS, MS/MS, and Multiplexed MS/MS Tissue Imaging
Oligonucleotide analysis by Linear MALDI-TOF mass spectrometry Stephen J. Hattan , Kenneth C. Parker, Marvin L. Vestal; SimulTOF Systems, 60 Union Ave,
Introduction to MALDI-TOF MS
Lecture 9. MALDI/TOF. Introduction Matrix-assisted laser desorption/ionization (MALDI) is a soft ionization technique used in mass spectrometry, allowing.
High Performance MALDI-TOF Mass Spectrometry Marvin Vestal and Kevin Hayden Virgin Instruments Corp. Sudbury, MA.
Chapter 20 Molecular Mass Spectrometry. Introduction... Mass spectroscopy is perhaps one of the most widely applicable of all the analytical tools available.
Instrumental Chemistry Chapter 11 Atomic Mass Spectrometry.
Atomic Mass Spectrometry
PROTEIN IDENTIFICATION BY MASS SPECTROMETRY. OBJECTIVES To become familiar with matrix assisted laser desorption ionization-time of flight mass spectrometry.
MALDI-TOF-TOF with High Resolution Precursor Selection and Multiplexed MS-MS Poster Number ThP 618 Kevin Hayden, Stephen C. Gabeler, Mark Dahl and Marvin.
4. Mass Spectrometry Objectives:
TOF Mass Spectrometer &
Chapter 8 – Mass Spectrometry. Mass Spectrometry The mass spectrometer can be used for: – Quantitative analysis – as a sophisticated and very sensitive.
Comparison of chicken light and dark meat using LC MALDI-TOF mass spectrometry as a model system for biomarker discovery WP 651 Jie Du; Stephen J. Hattan.
PC4250 Secondary Ion Mass Spectrometry (SIMS). What is SIMS? SIMS is a surface analysis technique used to characterize the surface and sub-surface region.
Secondary ion mass spectrometry (SIMS)
Marvin Vestal and Kevin Hayden Virgin Instruments Corp. Sudbury, MA
Atomic Structure 2.2: The Mass Spectrometry. Operation of Mass Spec Describe and explain the operation of a mass spectrometer What’s it for? A mass spectrometer.
The nucleus. Rutherford's nuclear atom (1902 ‑ 1920) Ernest Rutherford was interested in the distribution of electrons in atoms. Two of his students,
Mass spectrometry and the PITZ Sven Lederer Technisches Seminar
Status of the Beamline Simulation A.Somov Jefferson Lab Collaboration Meeting, May 11, 2010.
Tissue Imaging by 5 kHz High-Performance MALDI-TOF Poster Number TP191 Christina Vestal 1, Kenneth Parker 1, Kevin Hayden 1, George Mills 1, Marvin Vestal.
Gerardo E. Cornejo M. Bonner Denton Scott Tilden Roger Sperline Denton Research Lab Department of Chemistry University of Arizona
Based on ionization of gas phase molecule followed by analysis of the masses of the ions produced. The Mass Spectrum: Graph of ion intensity versus mass-to-charge.
Marvin Vestal and Kevin Hayden SimulTOF Systems
MASS SPECTROMETRY. CONTENTS Prior knowledge Background information The basic parts of a mass spectrometer The four stages of obtaining a spectrum How.
The Apparatus…. Ionic target studies…. Neutral target studies…. Queens University Belfast University College London.
MS Calibration for Protein Profiles We need calibration for –Accurate mass value Mass error: (Measured Mass – Theoretical Mass) X 10 6 ppm Theoretical.
MS Intro. MS requires gas-phase ions, why? MS uses magnetic and electric fields to control the path of a compound based on mass to charge ratio (m/z)
7-1 Atomic Mass Spectroscopy General Features Mass Spectrometers §Sources Atomic mass spectroscopy determines elements by mass §Mass to charge ratio §Lower.
Mass spectrometry (Test) Mass spectrometry (MS) is an analytical technique that measures masses of particles and for determining the elemental composition.
Starter: Spec links 1.06–1.10. Green pens out! Spec links 1.06–1.10.
Mass Analyzers : Time-of-flight Mass Spectrometry CU- Boulder CHEM 5181 Mass Spectrometry & Chromatography Joel Kimmel Fall 2007.
Molecular Mass. Mass of Atom Measured in atomic mass unit (amu) 1 amu = 1.66 x g Defined by assigning the mass of 12 amu to the carbon-12 isotope.
An evaluation of the isotope ratio performance of an axial TOF - ICP - mass spectrometer F. Vanhaecke, L. Moens, R. Dams, L. Allen* and S. Georgitis* University.
CONTENTS Prior knowledge Background information The basic parts of a mass spectrometer The four stages of obtaining a spectrum How different ions are deflected.
Rutherford Backscattering Spectrometry (RBS)
An electron/positron energy monitor based on synchrotron radiation. I.Meshkov, T. Mamedov, E. Syresin, An electron/positron energy monitor based on synchrotron.
Chem. 133 – 2/16 Lecture. Announcements Lab today –Will cover last 4 set 2 labs + start on set 2 labs –Lab Report on electronics labs – due 2/23 (I planned.
Chem. 133 – 2/18 Lecture. Announcements Homework Set 1.2 (bold problems) – due today Quiz 2 Today Electronics Lab Reports – due Tuesday Seminar this Friday.
Mass Spectrometry Relative atomic masses and the mass of individual isotopes can be determined using a mass spectrometer. The principle behind mass spectrometry.
Quantitative MALDI-TOF for Clinical Applications.
2014 생화학 실험 (1) 6주차 실험조교 : 류 지 연 Yonsei Proteome Research Center 산학협동관 421호
Chapter 29 Mass Spectrometry. 29 A Principles of mass spectrometry In the mass spectrometer, analyte molecules are converted to ions by applying energy.
Prepared by Lawrence Kok Tutorial on Mass Spectrometer and Isotopes.
What is Mass Spectrometry? Mass spectrometry could be considered as an analytical technique that involves the study in the gas phase of ionized molecules.
Atomic Structure Topic The mass spectrometer Describe and explain the operation of a mass spectrometer Describe how the mass spectrometer.
Yonsei Proteome Research Center Peptide Mass Finger-Printing Part II. MALDI-TOF 2013 생화학 실험 (1) 6 주차 자료 임종선 조교 내선 6625.
이 장 우. 1. Introduction  HPLC-MS/MS methodology achieved its preferred status -Highly selective and effectively eliminated interference -Without.
Atomic Structure Topic 2.
Dissociation of Molecular Ions Studied by
Components of Mass Spectrometer
Department of Tandem Accelerators
Acknowledgements Slides and animations were made by Dr. Jon Karty Mass Spectrometry Facility Indiana University, Bloomington.
Mass Spectrometry.
Starter Complete the quiz and hand in..
the s process: messages from stellar He burning
Chem. 133 – 2/16 Lecture.
Instrumental Chemistry
Mass Spectrometry.
Lecture 22 Introduction to Mass Spectrometry Lecture Problem 7 Due
Mass Spectrometry CHEM HONORS.
Stoichiometry- Mass Relationships in Chemical Reactions
Mass Spectrometry THE MAIN USE OF MS IN ORG CHEM IS:
M.Prasad Naidu MSc Medical Biochemistry, Ph.D,.
Presentation transcript:

Overall efficiency and speed of analysis – key factors are ions per sample molecule desorbed and ions produced per laser pulse Precision and accuracy of the ratio measurements – ion statistics dictate that for an average signal/shot of 100 summed over 10,000 yields ~0.1% precision. This has been demonstrated for 46 Ca at the natural abundance (40 ppm). Precision of 3.2% for 41 Ca at part per trillion abundance requires detection of 1000 ions from 41 Ca; this corresponds to production of ions from 40 Ca in 10 6 laser shots. We are developing 1 a multi-stage time-of- flight mass spectrometer (TOFMS) that uses laser desorption from solids to obtain accurate relative isotopic abundances at very low levels. A potential analytical target is 14 C in radiocarbon dating and biological tracer studies. Another important possible target is the 41 Ca isotope in studies of human bone production and loss. Given its very long half- life (>10 5 yr), radioactive 41 Ca is safe to administer to humans and can serve as a sensitive tracer if measurements of to relative abundance can be achieved. Although accelerator mass spectrometry (AMS) has demonstrated the utility of such measurements for both 14 C and 41 Ca, proliferation of applications has been limited by the relatively high cost and inaccessibility of the complex AMS instruments. We report here preliminary studies demonstrating feasibility for use of laser desorption TOFMS instruments for such applications. The much lower cost of these instruments compared to ASM makes them an attractive alternative for use in clinical settings. Measuring the Relative Abundance of Low-Level Isotopes With Laser Desorption Time-of-Flight Mass Spectrometry Poster Number MP 527 P. Jane Gale, Kevin Hayden, and Marvin L. VestalVirgin Instruments, Sudbury, MA Instrument Design: Three-Stage TOF for determination of isotope ratios Introduction The instrument design includes a two-field source with a set of ion deflectors allowing on-axis laser irradiation and trajectory compensation required for the large final deflection angle. It also includes two Bradbury Nielson mass gates, the 1 st located at the source focus and the 2 nd located at the focal point of the first of two 2-field ion mirrors. The 1 st gate rejects all but the narrow range of ions of interest for the isotope measurement, while the 2 nd gate selects individual ions that are then focused to one of three ion detectors with the second ion mirror. A pair of pulsed ion deflectors located at the exit of the second ion mirror gates selected ions to one of the three detectors. The ion detector system consists of one faraday cup and 2 ETP MagneTOF electron multipliers all connected to an Acqiris AP240 2channel 2 GHz averager. ETP detectors are rotated relative to the final gated deflection angle for trajectory error compensation. The instrument is designed for bipolar operation. Timing of ion source mass gates and pulsed detectors and averager are synchronized to the 5 kHz laser and controlled by a computer –controlled multichannel generator with 1 nsec precision and accuracy. Potential Interferences with 41 CaF + & 46 CaF + IonMass (da)RP Req’d 41 CaF ref 41 KF ,000* 60 Ni ,005 C2O2H4+C2O2H CoH ,050 Na 37 Cl ,973* 58 FeH , SC 2 H , PC 2 H , SiO , CaF ref AlF Potential Interferences with 41 CaF 3 - & 46 CaF 3 - IonMass (da)RP Req’d 41 CaF ref C 2 H 4 NO Ru Mo CaF ref 103 Rh AlF Results of Preliminary Studies CaF + or CaF 3 - ions are produced by laser bombardment of CaF 2 standards (~10 mg) deposited in wells on gold-coated plates and covered with a thin layer of paraffin. Detector gains are set for the ion intensity anticipated, based on relative abundances. *not expected to be stable under laser desorption conditions Resolving power of ~5000 is sufficient to eliminate most anticipated interferences Next Steps Explore alternative ion production techniques to enhance sensitivity Investigate sample preparation procedures appropriate to the clinical settings in which the instrument will operate Add TDC for measuring low level signal by ion counting Key Instrument Parameters 2-field source 3 mm each; flight path ~3.5 m Deflection angle: 1.5°; Detectors 1&3 off-center by ±2.25° Acc Volt: 8kV Laser: Explorer 5kHz, ~100 µJ/pulse; Pulse width 5 nsec; spot size ~30 µm 46CaF+- AlF3+ resolved x~25, CaF + signal from 41 Ca-enriched (1x10 -6 ) CaF 2 Standard 40 CaF + 42 CaF + 43 CaF + 44 CaF + 48 CaF + ScF + ? CaF 2 Spectrum Showing CaF + Isotopes x 50 Noise in 41CaF+ Channel 1000 spectra x 1000 shots CaF + AlF CaF + rejected by TIS 41 CaF signal ~5 ions/2000 shots for 1 ppm standard 1 ns Noise is due to mismatch between digitizer channels – no scattered ions detected Performance Challenge Very high abundance sensitivity required. Must detect an ion in the presence of a huge excess of another. This work is supported by grant R43RR from NCRR NIH. We thank Dr. Darren Hillengonds from LLNL for a gift of the enriched standard, and Dr. David Herold for many helpful discussions. Present Status: Resolving power sufficient to remove potential interferences; abundance sensitivity appears feasible; But we need to increase ionization rate by ca for practical applications.