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Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. [email protected] http:// msf.chem.indiana.edu

Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. [email protected]

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Page 1: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Why Mass Spectrometry: An Introduction to the IU MSF

Jonathan A. Karty, [email protected]

http://msf.chem.indiana.edu

Page 2: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Why Mass Spectrometry

• Information is composition-specific– Very selective analytical technique– Most other spectroscopies can describe

functionalities, but not chemical formulae• MS is VERY sensitive– mg/L to ng/L sensitivity possible– Picomole sensitivity is common in the MSF

• Mass spectrometers have become MUCH easier to use in the last 15 years

Page 3: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Three Questions• Did I make my compound?– Molecular weight is an intrinsic property of a substance

• Did I make anything else?– Mass spectrometry is readily coupled to chromatographic

techniques

• How much of it did I make?– Response in the mass spectrometer is proportional to

analyte concentration (R = α[M])• Each compound has a unique response factor, α

Page 4: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Common MS Applications

• Quick product identification (TLC spot)• Confirmation of elemental composition– Much more precise then EA

• Selective detector for GC/HPLC– MS provides retention time AND molecular weight

information about each analyte• Reaction monitoring– Crude reaction mixture MS– Stable isotope labeling– Stability studies

Page 5: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Important Concepts to Remember• Mass spectrometers analyze gas-phase ions, not

neutral molecules– Neutral molecules don’t respond to electromagnetic fields– If you cannot make a stable ion, MS is impossible

• MS is not a “magic bullet” technique– MS can tell you composition of an ion (CxHyOz)– Connectivity of the atoms in that ion is much more

challenging

• Units– 1 Da = 1 u = 1.6605*10-27 kg (1/12 of a 12C atom)– 1 Th = 1 Da/e = 1.0364*10-8 kg/C

Page 6: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Molecular Weight Calculations• The molecular weight is computed by summing the

masses of all atoms in the compound/ion.– Erythromycin (M+H)+: C37H68N1O13

+ = 12.011*37 + 1.008*67 +

14.007 + 15.999*13 = 734.93 Da

• Yet 734.5 is observed by ESI-MS

O

O

O

O

O

OH

O

NH+HOO

OH

OHHO

Page 7: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Isotopic Distributions• Isotopes: same number of protons, different numbers

of neutrons– 12C has 6 of each, 13C has 6 protons and 7 neutrons– Periodic table assumes a natural distribution of stable

isotopes (weighted average)

• Carbon isotopes– C 12C is 98.9% abundant, 13C is 1.1% abundant

• (0.989 * 12.0000) + (0.011 * 13.0034) = 12.011– For C40: 64.2% 13C0, 28.6% 13C1, 6.2% 13C2

• Spectrum looks like 100% @ 480, 44.5% @ 481, 9.6% @ 482

• Many elements have a variety of isotopes– Sn has 7 naturally occurring isotopes – F, P, Na, I, Co, Au have only 1 natural isotope

Unregistered

485484483482481480479

100

90

80

70

60

50

40

30

20

10

0

C40 mass spectrum

Page 8: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Monoisotopic Masses• Monoisotopic masses are considered for mass

spectrometry– Monoisotopic masses are computed using the most

abundant isotope of each element (12C, 35Cl, 14N, 16O, 79Br, 11B, 120Sn etc)

• For erythromycin, monoisotopic mass = 734.468– 12C37

1H68 14N1

16O13– 12.000 * 37 + 1.0078 * 68 + 14.0031 + 15.9949 * 13

• Remember to include any ionizing reagent– Electron loss, proton addition, etc.

Page 9: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

C37H68NO13+ Mass Spectrum

Average mass = 734.93 u

13C0, 2H0, 18O0

13C1, 2H0, 18O013C2, 2H0, 18O0

13C0, 2H0, 18O1

13C1, 2H1, 18O0

Observed isotope pattern is the convolution of isotope patterns for all atoms

Page 10: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Isotopic Envelopes• Isotopic distributions can indicate/preclude the

presence of an element– Cl has a unique 3:1 pattern (M:M+2)– B has a unique 1:4 pattern (M-1:M)

• M+1 / M+ ratio can be used to count carbon atoms in a molecule– [(M+1) / M+] / 0.011 ≈ # carbon atoms– For morphine: (0.1901 / 1) / 0.011 = 17.28 17

• Significant deviation from expected isotope pattern should be a warning sign– Multiple compounds with similar masses in sample– Partial isotopic enrichment (e.g. deuterated solvents used)– Multiple ionization mechanisms at work

Page 11: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Inte

ns

ity

(%

)

0

20

40

60

80

100

Mass [amu]362 364 366 368 370 372 374 376 378

Inte

ns

ity

(%

)

0

20

40

60

80

100

Mass [amu]131 132 133 134 135 136 137 138 139

Two Complex Isotope Patterns

C2H3Cl3

trichloroethane

C12H27SnBrtributyltin bromide

Monoisotopic mass: 131.93Average mass: 133.43

Monoisotopic mass: 370.03Average mass: 369.96

Page 12: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Instrumentation in the MSF

• One of 3 mass spectrometry facilities in the department• MSF is in Chemistry A411 and A454• 1 GC-EI-Q-MS (A454)• 1 LC-ESI/APCI-Q-MS (A454)• 2 LC-ESI-TOF-MS (A411)• 1 MALDI-TOF-MS (A411)• 1 EI/CI-BE-MS (A411, staff only)• Self-run experiments are $7-$10 per sample• Staff-run experiments are $16-$30• Training for Walk-Up MS will start after 11/7/10

Page 13: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Agilent 6890/5973 GC-MS

• 6890 GC– 30 m long DB-5 (non-

polar) column installed• Helium mobile phase

– Split/splitless injector with autosampler

• 5973 MS– Electron ionization – Quadrupole MS (10-800)– NIST 02 library installed

Page 14: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Agilent 1200/6130 LC-MS

• 1200 HPLC– Binary pump

• 0.05-2 mL/min

– Autosampler with 6-position column selector

– Diode array UV-VIS detector

• 6130 MS– Dual mode

electrospray/APCI source• Can perform all 4 modes of

ionization in 1 experiment

– 50-3,000 m/z quadrupole

• Easy Access Software

Page 15: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Waters CapLC-LCT LC-MS

• CapLC– Flow rates 1-40 uL/min– C18, C8, and C4 columns– Single wavelength UV-VIS

detector

• LCT– Electrospray ionization– Time-of-flight MS (TOF)

• 100-6,000 m/z

– Capable of accurate mass spectrometry • 5 ppm error for formula

confirmation

Page 16: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Bruker Autoflex III

• MALDI-TOF mass spectrometer– 200-150,000 m/z

• Can make both positive and negative ions from same spot

• Easy to interpret mass spectra for large polymers

• Matrices available for wide array of analytes

Page 17: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Thermo MAT-95XP

• Magnetic sector mass spectrometer

• Accurate mass spectrometry is its main function

• Electron ionization and Chemical ionization sources

• Trace GC available for low MW species or mixture analysis

Page 18: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Accurate Mass Spectrometry• Accurate mass spectrometry can unambiguously

confirm chemical composition

• Mass accuracy is often reported as a relative value – ppm = parts per million, 1 ppm = 0.0001%

• 5 ppm error is used by many journals as a standard to confirm a chemical formula– Instrumentation in the IU MSF routinely achieves this

level of accuracy– 5 ppm at mass 300: 300 * (5/106) = ±0.0015 Da

Page 19: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Formula Matching Basics• Atomic weights are not integers (except 12C)– 14N = 14.0031 Da; 1H = 1.0078 Da– 16O = 15.9949 Da; 127I = 126.9045 Da– Table of isotopes link on MSF website

• Difference from integer mass is called “mass defect”– Related to nuclear binding energy (E = mc2)

• Sum of the mass defects depends on formula– H, N increase mass defect

• Eicosane (C20H42) = 282.3286

– O, Cl, F, Na decrease it• Morphine (C17H19NO3) = 285.1365

Page 20: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

More Formula Matching• Accurate mass measurements narrow down possible

formulas for a given molecular weight– 534 entries in NIST’08 library @ mass 285– Only 3 formulas within 5 ppm of 285.1365

• 46 compounds with formula C17H19NO3

• Mass spectrum and user info complete the picture– Isotope distributions indicate / eliminate elements – User - supplied info eliminates others (e.g. no F)– Suggested formula has to make chemical sense

Page 21: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Formula Matching Example

Only 9 ways to combine up to 40 C, 50 H, 5 N, 5 O, and 2 Cl to get a mass within 20 ppm (0.0061 u) of 306.0820, only 3 have 2 Cl

Elemental Composition ReportTolerance = 20.0 PPM / DBE: min = -1.5, max = 50.0Selected filters: NoneMonoisotopic Mass, Even Electron Ions370 formulas evaluated with 9 results within limitsElements Used:C: 0-40 H: 0-50 N: 0-5 O: 0-5 Cl: 0-2 Error 20 ppm

Mass intensity Calc. Mass mDa PPM i-FIT

306.082 100 306.0816 0.4 1.3 39.7 C17 H18 N Cl2 306.0776 4.4 14.4 376 C12 H18 N3 O2 Cl2 306.0875 -5.5 -18 701.7 C10 H22 N O5 Cl2 306.0798 2.2 7.2 1945.8 C18 H13 N3 Cl 306.0857 -3.7 -12.1 2205.2 C11 H17 N3 O5 Cl 306.0766 5.4 17.6 9102.8 C18 H12 N O4 306.078 4 13.1 9195.6 C19 H8 N5 306.0879 -5.9 -19.3 9289.5 C17 H12 N3 O3 306.0838 -1.8 -5.9 9543.2 C12 H12 N5 O5

error in:Formula

Zoloft C17H18Cl2N

Page 22: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Accurate MS Notes

• Accurate MS is possible with the MAT-95 and LCT mass spectrometers– Bruker MALDI-TOF can do 20 ppm mass accuracy

• Only MSF staff can perform accurate mass measurements

• All accurate MS submissions MUST include a nominal (low res) mass spectrum to demonstrate purity PRIOR to accurate MS

Page 23: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Sample LCT Accurate Mass Report

Page 24: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Sample MAT-95 Accurate Mass Report

Page 25: Why Mass Spectrometry: An Introduction to the IU MSF Jonathan A. Karty, Ph.D. jkarty@indiana.edu

Upcoming Lectures• All in C033 from 5:30-6:15• Small molecule EI and GC-MS (10/14)• Small molecule ESI/APCI and LC-MS (10/18)• Biomolecule/polymer analysis by ESI and MALDI

(10/20)• Possible special interest seminars in November– Quantitation and other advanced topics for small molecule

MS– Intro to Bioinformatics– These will only occur if sufficient interest is expressed

• For a more in-depth treatment of all topics covered, take C613 in the spring!