The Future of Time-of-flight Mass Spectrometry

Slides:



Advertisements
Similar presentations
High Performance MALDI MS, MS/MS, and Multiplexed MS/MS Tissue Imaging
Advertisements

Improvements in Mass Spectrometry for Life Science Research – Does Agilent Have the Answer? Ashley Sage PhD.
Les détecteurs de masse : une révolution en chromatographie 1ère partie : Introduction à la spectrométrie de masse Pr. Jean-Louis Habib Jiwan UCL – Département.
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
Mass Spectrometry Inlet system Ion Source Mass Analyzer Ion Detector.
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.
Development of TOF-MS from intellectual curiosity to practical technique Marvin Vestal SimulTOF Systems The Jim Waters Symposium at PittCon March 2, 2014.
How to identify peptides October 2013 Gustavo de Souza IMM, OUS.
MALDI MS Imaging on the 4800 MALDI TOF/TOF™ Analyzer Prepared by Andrew James, PhD.
Chem. 133 – 4/28 Lecture. Announcements Lab Report 2.3 due Today Pass back graded materials (lab reports 2.2, Q5, and AP3.1) Today’s Lecture Mass Spectrometry.
Mass Spectrometry. How is MS Done? Basic MS Instrumentation.
Mass Analyzers Double Focusing Magnetic Sector Quadrupole Mass Filter Quadrupole Ion Trap Linear Time-of-Flight (TOF) Reflectron TOF Fourier Transform.
Mass Spectrometry in the Biosciences: Introduction to Mass Spectrometry and Its Uses in a Company Like Decode. Sigurður V. Smárason, Ph.D. New Technologies.
Proteomics The proteome is larger than the genome due to alternative splicing and protein modification. As we have said before we need to know All protein-protein.
PROTEIN IDENTIFICATION BY MASS SPECTROMETRY. OBJECTIVES To become familiar with matrix assisted laser desorption ionization-time of flight mass spectrometry.
Beta-Galactosidase Digest from 500 fmole Loaded on a 1-D Gel A. B. C. Bovine Serum Albumin Digest from 250 fmole Loaded on a 1-D Gel Automation of In-Gel.
Mass Labels While Mass Spectroscopy is not covered in our texts, other mass/density dependent technologies including X-ray Spectroscopy, Gamma Spectroscopy,
Molecular Mass Spectrometry
LC-MS Lecture 7.
Mass Spectroscopy Quantitative Chemical Analysis Harris, 6th Edition
Photoelectron Spectroscopy Lecture 7 – instrumental details –Photon sources –Experimental resolution and sensitivity –Electron kinetic energy and resolution.
Basics of 2-DE and MALDI-ToF MS
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.
Proteomics Informatics – Overview of Mass spectrometry (Week 2)
Tryptic digestion Proteomics Workflow for Gel-based and LC-coupled Mass Spectrometry Protein or peptide pre-fractionation is a prerequisite for the reduction.
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.
The ProteomeWorks System is the global alliance of Micromass and Bio-Rad Laboratories dedicated to furthering proteomics research.
Introduction Recent research has proposed rapid and robust identification of intact microorganisms using matrix assisted laser desorption/ ionization time-of-flight.
Chapter 9 Mass Spectrometry (MS) -Microbial Functional Genomics 조광평 CBBL.
Marvin Vestal and Kevin Hayden Virgin Instruments Corp. Sudbury, MA
Molecular mass spectrometry Chapter 20 The study of “molecular ions” M + e -  M e -
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.
Mass Spectrometry I Basic Data Processing. Mass spectrometry A mass spectrometer measures molecular masses. The mass unit is called dalton, which is 1/12.
UPDATE! In-Class Wed Oct 6 Latil de Ros, Derek Buns, John.
INF380 - Proteomics-61 INF380 – Proteomics Chapter 6 – Mass Spectrometry – MALDI TOF The MALDI-TOF instruments are the simplest MS instruments suitable.
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.
-Aluminum housing with o-ring seal allows for washing (salt removal), plate cleaning and regeneration enabling for multiple use -Sample elution for MS.
Marvin Vestal and Kevin Hayden SimulTOF Systems
A new "Molecular Scanner" design for interfacing gel electrophoresis with MALDI-TOF ThP Stephen J. Hattan; Kenneth C. Parker; Marvin L. Vestal SimulTof.
For all CHEM5161 students: The first day of class for CHEM5161 (Analytical Spectroscopy) will be on TUE Sept 4 (following Labor Day). There will be no.
INF380 - Proteomics-51 INF380 – Proteomics Chapter 5 – Fundamentals of Mass Spectrometry Mass spectrometry (MS) is used for measuring the mass-to-charge.
MALDI demonstration Frímann, Helgi, Long, Nanna. Sample preperation The sample of interest and matrix are dissolved in a volatile solvent The sample/matrix/solvent.
Mass Analyzers : Time-of-flight Mass Spectrometry CU- Boulder CHEM 5181 Mass Spectrometry & Chromatography Joel Kimmel Fall 2007.
Pulsed Field Gel Electrophoresis In normal electrophoresis - electrophoretic mobility is independent of molecular weight for large DNA (> 50 kbp) elongate.
A versatile MALDI target plate based on polymer-filled reticulated vitreous carbon foam ThP Stephen J. Hattan ; Jie Du; Kenneth C. Parker VIC Instruments.
Separates charged atoms or molecules according to their mass-to-charge ratio Mass Spectrometry Frequently.
Quantitative MALDI-TOF for Clinical Applications.
Chem. 133 – 4/26 Lecture. Announcements Return graded quiz and additional problem Lab – Lab report deadlines (2:4 – Thursday) Today’s Lecture – Mass Spectrometry.
2014 생화학 실험 (1) 6주차 실험조교 : 류 지 연 Yonsei Proteome Research Center 산학협동관 421호
What is Mass Spectrometry? Mass spectrometry could be considered as an analytical technique that involves the study in the gas phase of ionized molecules.
RANIA MOHAMED EL-SHARKAWY Lecturer of clinical chemistry Medical Research Institute, Alexandria University MEDICAL RESEARCH INSTITUTE– ALEXANDRIA UNIVERSITY.
Yonsei Proteome Research Center Peptide Mass Finger-Printing Part II. MALDI-TOF 2013 생화학 실험 (1) 6 주차 자료 임종선 조교 내선 6625.
An introduction to Mass spectrometry. What is mass spectrometry? Analytical tool measuring molecular weight (MW) of sample Only picomolar concentrations.
Post translational modification n- acetylation Peptide Mass Fingerprinting (PMF) is an analytical technique for identifying unknown protein. Proteins to.
Peptide Mass Finger-Printing Part II. MALDI-TOF
Mass Spectrometry 101 (continued) Hackert - CH 370 / 387D
Acknowledgements Slides and animations were made by Dr. Jon Karty Mass Spectrometry Facility Indiana University, Bloomington.
Chem. 133 – 4/13 Lecture.
The Covalent Structure of Proteins
Time of Flight Analyzers
S. Emonet, H.N. Shah, A. Cherkaoui, J. Schrenzel 
Time-of-Flight Mass Analyzers
Figure 1 Schematic representation of a typical MALDI-MSI workflow
S. Emonet, H.N. Shah, A. Cherkaoui, J. Schrenzel 
A, schematic presentation of fetuin-A domains.
Pierre P. Massion, MD, Richard M. Caprioli, PhD 
Mass Spectrometry THE MAIN USE OF MS IN ORG CHEM IS:
Investice do rozvoje vzdělávání
Presentation transcript:

The Future of Time-of-flight Mass Spectrometry Marvin Vestal Applied Biosystems Framingham, MA

A Brief History of Time (of flight) with apologies to Stephen Hawking 1946 W.E Stephens, Phys. Rev. 69,641 “Advances in electronics seem to make practical a type of mass spectrometer in which microsecond pulses of ions are selected every millisecond from an ordinary low-voltage ion source. In travelling down the vacuum tube, ions of different M/e have different velocities and consequently separate into groups spread out in space. … This type of mass spectrometer should offer many advantages over present types. The response time should be limited only by the repetition rate (milliseconds)… Magnets and stabilization equipment would be eliminated. Resolution would not be limited by smallness of slits or alignment. Such a mass spectrometer should be well suited for composition control, rapid analysis, and portable use.”

Brief History of Time (of flight) 1948 Cameron & Eggers, Rev. Sci. Instr. 19, 605. First working TOF 1953 Wiley & McLaren, Rev. Sci. Instr. 26, 1150 First practical TOF. Energy & Time Lag Focusing. 1959 Gohlke, Anal. Chem. 31, 535 GC-TOF 1963 Vestal & Wharhaftig, ASMS, 358. Coincidence TOF, first ion counting TDC 1973 Mamyrin et al, Sov. Phys. JETP 37, 45. Reflectron, higher resolution 1974 Macfarlane et al, Biochem. Biophys. Res. Comm. 60, 616 252Cf Plasma desorption. Proteins Fly!!!!

Brief History of Time (of flight) 1988 Karas & Hillenkamp, Anal. Chem. 60, 2299. MALDI - Really big proteins fly!!! 1991 Dodenov et al, 12th Int. MS Conf. O-TOF - Electrospray works with TOF 1993 Kaufman, Spengler & Lutzenkirchen, RCM 7, 902. Post-source dcay MALDI 1994 Brown & Lennon, Sunriver, p63. Delayed extraction MALDI - Makes MALDI-TOF routine 1996 Morris et al, RCM 10, 889. Q-TOF 2001 TOF-TOF

Today’s Instruments Ionization Techniques TOF Analyzers Electrospray o-TOF Qq-o-TOF MALDI linear TOF reflector TOF TOF-TOF Trap-TOF

Why TOF? Speed Efficiency (Sensitivity) Dynamic Range Resolving Power Mass Accuracy Mass Range Simplicity Competitive in All Respects with Unmatched Speed

Speed Matters! Particularly with MALDI More Samples - Higher Throughput More Measurements/Sample Better data - Precision of mass and intensity Increased dynamic range

MALDI-TOF yesterday, today, and tomorrow then now future Laser Rate (hz) 2 200 10,000 Acq. Time/Spect.(sec) 60 2 0.1 Spectra/day 1000 40,000 1,000,000* *If we can process and interpret the results Applications Better sample utilization (>100,000 shots/spot) Interface with separations Molecular scanner Tissue Imaging 1 cm2 @100 micron resolution =10,000 pixels

50 Laser shots in 0.25 sec on 125 femtomoles of trypic digest

E Coli beta-galactosidase, MW 116,483.9 16/20 matched, MOWSE Score 3e14, 23% sequence coverage 1 11 21 31 41 51 61 71 MTMITDSLAV VLQRRDWENP GVTQLNRLAA HPPFASWRNS EEARTDRPSQ QLRSLNGEWR FAWFPAPEAV PESWLECDLP 81 91 101 111 121 131 141 151 EADTVVVPSN WQMHGYDAPI YTNVTYPITV NPPFVPTENP TGCYSLTFNV DESWLQEGQT RIIFDGVNSA FHLWCNGRWV 161 171 181 191 201 211 221 231 GYGQDSRLPS EFDLSAFLRA GENRLAVMVL RWSDGSYLED QDMWRMSGIF RDVSLLHKPT TQISDFHVAT RFNDDFSRAV 241 251 261 271 281 291 301 311 LEAEVQMCGE LRDYLRVTVS LWQGETQVAS GTAPFGGEII DERGGYADRV TLRLNVENPK LWSAEIPNLY RAVVELHTAD 321 331 341 351 361 371 381 391 GTLIEAEACD VGFREVRIEN GLLLLNGKPL LIRGVNRHEH HPLHGQVMDE QTMVQDILLM KQNNFNAVRC SHYPNHPLWY 401 411 421 431 441 451 461 471 TLCDRYGLYV VDEANIETHG MVPMNRLTDD PRWLPAMSER VTRMVQRDRN HPSVIIWSLG NESGHGANHD ALYRWIKSVD 481 491 501 511 521 531 541 551 PSRPVQYEGG GADTTATDII CPMYARVDED QPFAVPKWS IKKWLSLPGE TRPLILCEYA HAMGNSLGGF AKYWQAFRQY 561 571 581 591 601 611 621 631 PRLWGGFVWD WVDQSLIKYD ENGNPWSAYG GDFGDTPNDR QFCMNGLVFA DRTPHPALTE AKHQQQFFQF RLSGQTIEVT 641 651 661 671 681 691 701 711 SEYLFRHSDN ELLHWMVALD GPKPLASGEVP LDVAPQGKQL IELPELPQPE SAGQLWLTVR VVQPNATAWS EAGHISAWQQ 721 731 741 751 761 771 781 791 WRLAENLSVT LPAASHAIPH LTTSEMDFCI ELGNKRWQFN RQSGFLSQMW IGDKKQLLTP LRDQFTRAPL DNDIGVSEAT 801 811 821 831 841 851 861 871 RIDPNAWVER WKAAGHYQAE AALLQCTADT LADAVLITTA HAWQHQGKTL FISRKTYRID GSGQMAITVD VEVASDTPPHP 881 891 901 911 921 931 941 951 ARIGLNCQLA QVAERVNWLG LGPQENYPDR LTAACFDRWD LPLSDMYTPY VFPSENGLRC GTRELNYGPH QWRGDFQFNI 961 971 981 991 1001 1011 1021 SRYSQQQLME TSHRHLLHAE EGTWLNIDGF HMGIGGDDSW SPSVSAEFQL SAGRYHYQLV WCQK

1000 Laser shots(5 seconds)

10,000 laser shots, increased gain Low masses suppressed (50 seconds) 975-1014 563-600

10,000 laser shots Focused at low mass (50 seconds) 290-293 VTLR ? 335-337 EVR

Summary of Database Searching Results 1000 Laser Shots, 20 ppm window m/z No. No. Match Seq.Cov. Mean Error Data Tol. S/N Sub. Match % % ppm ppm 1000-3000 100 18 14 78 19 1.65 9.0 30 29 23 79 36 1.56 8.3 10 49 33 67 45 1.07 8.9 3 196 52 27 53 0.60 15.0 3000-10000 10 26 9 35 31 -2.18 10.8 400-1000 30 7 5 71 3 -7.58 13.9 10 18 11 61 5 -6.02 9.8 3 156 24 15 12 -5.01 15.4 Total 3 378 85 23 96

Peaks detected down to S/N =3 52/196 matched M/z 1000-3000, 1000 laser shots Peaks detected down to S/N =3 52/196 matched Number of Peptides Matched -20 -18 -16 -14 -12 -10 -8 -6 -4 -2 0 2 4 6 8 10 12 14 16 18 Error (ppm)

E Coli beta-galactosidase, MW 116,483.9 50 shots 1000 shots high mass low mass 1 11 21 31 41 51 61 71 MTMITDSLAV VLQRRDWENP GVTQLNRLAA HPPFASWRNS EEARTDRPSQ QLRSLNGEWR FAWFPAPEAV PESWLECDLP 81 91 101 111 121 131 141 151 EADTVVVPSN WQMHGYDAPI YTNVTYPITV NPPFVPTENP TGCYSLTFNV DESWLQEGQT RIIFDGVNSA FHLWCNGRWV 161 171 181 191 201 211 221 231 GYGQDSRLPS EFDLSAFLRA GENRLAVMVL RWSDGSYLED QDMWRMSGIF RDVSLLHKPT TQISDFHVAT RFNDDFSRAV 241 251 261 271 281 291 301 311 LEAEVQMCGE LRDYLRVTVS LWQGETQVAS GTAPFGGEII DERGGYADRV TLRLNVENPK LWSAEIPNLY RAVVELHTAD 321 331 341 351 361 371 381 391 GTLIEAEACD VGFREVRIEN GLLLLNGKPL LIRGVNRHEH HPLHGQVMDE QTMVQDILLM KQNNFNAVRC SHYPNHPLWY 401 411 421 431 441 451 461 471 TLCDRYGLYV VDEANIETHG MVPMNRLTDD PRWLPAMSER VTRMVQRDRN HPSVIIWSLG NESGHGANHD ALYRWIKSVD 481 491 501 511 521 531 541 551 PSRPVQYEGG GADTTATDII CPMYARVDED QPFAVPKWS IKKWLSLPGE TRPLILCEYA HAMGNSLGGF AKYWQAFRQY 561 571 581 591 601 611 621 631 PRLWGGFVWD WVDQSLIKYD ENGNPWSAYG GDFGDTPNDR QFCMNGLVFA DRTPHPALTE AKHQQQFFQF RLSGQTIEVT 641 651 661 671 681 691 701 711 SEYLFRHSDN ELLHWMVALD GPKPLASGEVP LDVAPQGKQL IELPELPQPE SAGQLWLTVR VVQPNATAWS EAGHISAWQQ 721 731 741 751 761 771 781 791 WRLAENLSVT LPAASHAIPH LTTSEMDFCI ELGNKRWQFN RQSGFLSQMW IGDKKQLLTP LRDQFTRAPL DNDIGVSEAT 801 811 821 831 841 851 861 871 RIDPNAWVER WKAAGHYQAE AALLQCTADT LADAVLITTA HAWQHQGKTL FISRKTYRID GSGQMAITVD VEVASDTPPHP 881 891 901 911 921 931 941 951 ARIGLNCQLA QVAERVNWLG LGPQENYPDR LTAACFDRWD LPLSDMYTPY VFPSENGLRC GTRELNYGPH QWRGDFQFNI 961 971 981 991 1001 1011 1021 SRYSQQQLME TSHRHLLHAE EGTWLNIDGF HMGIGGDDSW SPSVSAEFQL SAGRYHYQLV WCQK

Missing Peptides MH+ 811-812 WK 333. 338-353 IENGLLLLNGKPLLIR 1776.111 390-405 CSHYPNHPLWYTLCDR 2004.885 450-474 NHPSVIIWSLGNESGHGANHDALYR 2744.329 448-474 DRNHPSVIIWSLGNESGHGANHDALYR 3015.457

1776 257-283 358-381

IENGLLLLNGKPLLIR Sequence expected IENGLLLLDGKPLLIR Major component, labeled IEDGLLLLDGKPLLIR Minor component

CSHYPNHPLWYTLCDR b15-2 S

DRNHPSVIIWSLGNDSGHGANHDALYR E MH + = 3001.44 b23 b14 y24 b21

Summary of Results 99.8 % of Sequence Covered (1022 of 1024) AA at position 462 is D not E Intact disulfide bond at 390-403 Deamidation of NG at positions 340 and 346 Discussed by N. E.Robinson PNAS 2002, 99,5283 Dynamic range>1000 and resolving power>10,000 required to obtain good coverage Results required < 5 min. acquisition time on 125 fmoles loaded (51,000 laser shots @200 hz)

What will the future bring Laser rates to 10 khz will be routine within two years A major challenge is developing automated data acquisition, processing, and interpretation systems that can operate continuously at rates in the range of 10-100 finished spectra/sec. Applications to protein and peptide samples distributed on surfaces become practical 10,000 discrete spots/sample plate Multi-channel LC interfaced to single MALDI-TOF Molecular scanner for 1- and 2-D gels Direct tissue imaging