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The Chromatographic Side of LC-MS and its Consequences
11/03/12 Carr’s Group Meeting by Marcelo Filgueira
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Context
• In LC-MS you have to constrain the LC to get the benefits of MS
• When doing Fast Online LC×LC-MS we are pushing conditions to the limit
– Very high flow rates
– Ultra-fast gradients
– Injections into the 2D every 12-20 s
– Scan mode for non-targeted analysis
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Indoles mixture. DAD@220 nm, MSD TIC@100-700 Da, tc: 21 s, Active Splitter: 27 µL/min 2D column is SB-C18 30x2.1 3.5 um, 2tg: 18, 2F: 1.5 mL/min
LCxLC: DAD vs. MSD
DAD
MSD
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LCxLC: DAD vs. MSD
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Indoles mixture. DAD@220 nm, MSD TIC@100-700 Da, tc: 21 s, Active Splitter: 27 µL/min 2D column is SB-C18 30x2.1 3.5 um, 2tg: 18, 2F: 1.5 mL/min EIC: [email protected], [email protected], [email protected]
DAD@220 MSD TIC
EIC: 143.2 EIC: 204.2 EIC: 192.3
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Outline
• Background
• The Organic Modifier
• Acid Type and Concentration
• Effect of pH in Fragmentation
• Quality of the Solvents
• Matrix Effects and Ion Suppression
• Strategies To Reduce Matrix Effects
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Coupling LC with MS
• Atmospheric Pressure Ionization (API)
– Electrospray Ionization(ESI)
– Atmospheric Pressure Chemical Ionization (APCI)
– Atmospheric Pressure Photo-Ionization (APPI)
• ESI is currently the most widely used ionization source (80 % of publications with LC-MS)
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The amount of Ions going into the source will depend on
• ES efficiency
• Protonation of molecules
• Ions observed in the ES MS do not reflect the equilibrium concentrations of ions in solution*
7 * Hiraoka K., Murata K., and Kudaka I., J. Mass Spectrom. Soc. Jpn. , 1995, Vol. 43, No. 3
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The Organic Modifier
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Acetone, Methanol and Acetonitrile
Fritz, R.; Ruth, W.; Kragl, U. Rapid Communications in Mass Spectrometry 2009, 23, 2139–2145.
Acetonitrile with 0.1% formic acid; Methanol with 0.1% formic acid; Water with 0.1% formic acid (all LC/MS Chromatosolv) purchased from Riedel-de Haen (Seelze, Germany) Acetone (Baker ultra resi-analysed) from J.T.Baker (Deventer, The Netherlands).
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Acetone, Methanol and Acetonitrile
Chromatograms of a tryptic digest of BSA using (A) ACN, (B) MeOH, and (C) Acetone
Fritz, R.; Ruth, W.; Kragl, U. Rapid Communications in Mass Spectrometry 2009, 23, 2139–2145.
BioBasic C18, 2.1x150 mm, 5 um, 300A; Thermo Scientific
Gradient: 5% ACN in water (0.1% FA) for 10 min; linear gradient to 80% ACN in 40 min, hold for 5 min and back to 5% ACN in 5 min (Same for Methanol and Acetone) F: 150 uL/min @ 25 C.
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ACN MeOH
Acetone
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Acetone, Methanol and Acetonitrile
Fritz, R.; Ruth, W.; Kragl, U. Rapid Communications in Mass Spectrometry 2009, 23, 2139–2145. 11
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Acetone and Acetonitrile
• With respect to ESI, acetone has a lower surface tension and higher volatility than acetonitrile, suggesting that ESI would be more efficient with acetone than with acetonitrile
• Finally, we note that the price of acetone is comparable to methanol and roughly one-third that of acetonitrile (Fisher Optima grade)
Keppel, T. R.; Jacques, M. E.; Weis, D. D. Rapid Communications in Mass Spectrometry 2010, 24, 6–10. 12
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Acetone and Acetonitrile
Total ion chromatograms of the separation of the peptide retention standard. (c) C18 column with an 8–18% B acetonitrile/water gradient, and (d) C18 column with a 7–18% B acetone/water gradient. 50x1.0mm ZORBAX 300 SB-C18, 3.5 um, 300 A; F: 50 uL/min
Keppel, T. R.; Jacques, M. E.; Weis, D. D. Rapid Communications in Mass Spectrometry 2010, 24, 6–10. 13
ACN
Acetone
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Maximized signal intensity for each peptide dissolved in acetone/water/formic acid (25/75/0.1%).
Maximize signal intensity of peptides dissolved in acetonitrile/water/formic acid (25/75/0.1%) directly infused into the electrospray source.
Acetone was substituted for acetonitrile as the organic solvent and spectra were acquired with TOF settings unchanged from their acetonitrile-optimized settings.
Keppel, T. R.; Jacques, M. E.; Weis, D. D. Rapid Communications in Mass Spectrometry 2010, 24, 6–10.
ESI+ Efficiency: Solutions directly infused into the MSD
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Acetone and Acetonitrile
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Keppel, T. R.; Jacques, M. E.; Weis, D. D. Rapid Communications in Mass Spectrometry 2010, 24, 6–10.
ESI Efficiency: Optimized parameters
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Acetone and Acetonitrile
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Acetone and Acetonitrile
Comparing spectra in the m/z 50–500 region for these two solvent mixtures shows that acetone had a more complex mixture of ions at higher intensities.
Keppel, T. R.; Jacques, M. E.; Weis, D. D. Rapid Communications in Mass Spectrometry 2010, 24, 6–10.
Solvents from Fisher Scientific: Optima LC/MS grade ACN and Water Optima grade Acetone
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Acid Type and Concentration
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Influence of Acid Type and Concentration in ESI+ (Proteins)
Huber, C. G.; Premstaller, A. Journal of Chromatography A 1999, 849, 161–173. 18
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Influence of Acid Type and Concentration in ESI+ (Proteins)
Huber, C. G.; Premstaller, A. Journal of Chromatography A 1999, 849, 161–173. 19
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Effect of Weak Acids on ESI-
Wu, Z.; Gao, W.; Phelps, M. A.; Wu, D.; Miller, D. D.; Dalton, J. T. Analytical Chemistry 2004, 76, 839–847.
“…different acids had quite different effects on the negative-ion ESI responses of these compounds, indicating that the properties of the acid played an important role in analyte deprotonation.”
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Effect of Weak Bases on ESI-
Wu, Z.; Gao, W.; Phelps, M. A.; Wu, D.; Miller, D. D.; Dalton, J. T. Analytical Chemistry 2004, 76, 839–847. 21
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Effect of pH on MS/MS Fragmentation
…”These charge-site isomers have identical m/z values but different sites of proton attachment.
The different charge-site isomers can fragment independently and the resulting MS/MS spectrum in a given mobile phase is a composite of these product ion spectra and reflective of the mixture of ions present in the gas phase when electrosprayed from solution of a specific composition.”
Wang, J.; Aubry, A.; Bolgar, M. S.; Gu, H.; Olah, T. V.; Arnold, M.; Jemal, M. Rapid Communications in Mass Spectrometry 2010, 24, 3221–3229. 22
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Effect of pH on MS/MS Fragmentation
Wang, J.; Aubry, A.; Bolgar, M. S.; Gu, H.; Olah, T. V.; Arnold, M.; Jemal, M. Rapid Communications in Mass Spectrometry 2010, 24, 3221–3229. 23
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Effect of pH on MS/MS Fragmentation
Wang, J.; Aubry, A.; Bolgar, M. S.; Gu, H.; Olah, T. V.; Arnold, M.; Jemal, M. Rapid Communications in Mass Spectrometry 2010, 24, 3221–3229. 24
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Quality of the Mobile Phase
• The quality and suitability of all the mobile phase constituents must be considered because they all enter the ion source and influence ion generation. (1)
• In evaluating the response of 32-desmethoxyrapamycin using 9 brands of methanol from 5 different manufacturers, they demonstrated that the MS/MS peak area could vary by at least an order of magnitude (10-fold).(2)
(2) T.M. Annesley, Clin. Chem. 53 (2007) 1827.
(1) Gray, M. J.; Jahani, S.; Low, G. K.-C. Journal of Chromatography A 2012, 1219, 83–92.
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Gray, M. J.; Jahani, S.; Low, G. K.-C. Journal of Chromatography A 2012, 1219, 83–92.
Quality of the Mobile Phase
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Quality of the Mobile Phase
Gray, M. J.; Jahani, S.; Low, G. K.-C. Journal of Chromatography A 2012, 1219, 83–92. 27
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Quality of the Mobile Phase
Gray, M. J.; Jahani, S.; Low, G. K.-C. Journal of Chromatography A 2012, 1219, 83–92. 28
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Matrix Effects
• Matrix effects are the alteration of ionization efficiency by the presence of co-eluting substances
• The exact mechanism of matrix effects is unknown – Competition between nonvolatile matrix components
and analyte ions for access to the droplet surface for transfer to the gas phase
• The majority of matrix effects occur in the solvent front of a chromatographic run (careful….)
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Matrix Effects
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58.
+ 0.5% NH4OH
No additive
+ 0.5% TFA
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Matrix Effects: pH Additives
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 31
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Matrix Effects: Buffers
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 32
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Matrix Effects: Sample Clean-up
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 33
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Matrix Effects: Sample Clean-up
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 34
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Matrix Effects: Sample Clean-up
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 35
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Matrix Effects: Sample Clean-up
Mallet, C. R.; Lu, Z.; Mazzeo, J. R. Rapid Communications in Mass Spectrometry 2004, 18, 49–58. 36
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Matrix Effect of Blood and Sample Preparation Method
Taylor PJ, Johnson AG. J Chromatogr. B 1998;718:251–7. 37
Protein Precipitation
SPE
Baseline
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Approaches to Reduce Matrix Effects
Nováková, L. Challenges in the development of bioanalytical liquid chromatography–mass spectrometry method with emphasis on fast analysis. Journal of Chromatography A 2012. 38
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Reduced Matrix Effect by 2D-LC (sLCxLC)
SRM chromatogram from a 1D-LC separation SRM chromatogram from a sLCxLC separation
Groskreutz, S. R.; Swenson, M. M.; Secor, L. B.; Stoll, D. R. Journal of Chromatography A 2012, 1228, 41–50. 39
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Conclusions
• Acetone might be better than it was shown but definitively a viable alternative
• The choice of the additive is mode (ESI + or -) and sample dependent
• Matrix effects have to be addressed whenever possible • Biological samples clean-up is highly advisable (almost
mandatory…) • Quality of solvents is very important, especially in Scan
mode • Matrix effects can be reduced with more resolving
power
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Question:
• How can we improve the baseline in Fast Online 2D-LC?
– Consistent flow rate
– Balanced ionization in gradient solvents?
– Selective background removal method?
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