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commonMZ

This is a collection of common m/z values found in mass spectrometry. The tables are available through an R package. You can find the table files in the “inst” subfolder.

Contributions are welcomed.

It contains these tab delimited files:

  • contaminants_+.tsv: A table of common contaminant masses in positive ionization mode.
  • contaminants_-.tsv: A table of common contaminant masses in negative ionization mode.
  • adducts_fragments.tsv: A table of common fragment and adducts. The listed mass refers to mass differences.
  • repeating_units_+.tsv: A table of common series of repeated units (mass differences) in positive ionization mode.
  • repeating_units_-.tsv: A table of common series of repeated units (mass differences) in negative ionization mode.

And these excel files:

  • CAMERA_rules_pos.xlsx: A table of common fragment and adducts for use with CAMERA in positive mode. The listed mass refers to mass differences to the uncharged species.
  • CAMERA_rules_neg.xlsx: A table of common fragment and adducts for use with CAMERA in negative mode. The listed mass refers to mass differences to the uncharged species.
  • CAMERA_rules_EI.xlsx: A table of common fragment and adducts for use with CAMERA in EI mode. The listed mass refers to mass differences to the uncharged species.

Excel files are used to make it easier to work with since adducts/fragment types have been color coded.

Glossary

Type of ions: Explanation
f+ fragment ion
[f+H]+ protonated fragment ion, e.g. in-source fragmentation of peptide ions
[M+H]+ protonated molecular ion (pseudomolecular ion)
[M+Na]+ sodiated molecular ion
[M+K]+ potassiated molecular ion
[M2+H]+, [M3+H]+ etc… protonated dimeric, trimeric, etc… molecular ion
[AnBm+H]+ protonated molecular ion consisting of n A and m B subunits
Abbreviations Explanation
4-HCCA α-cyano-4-hydroxycinnamic acid, common matrix substance for MALDI MS analysis
2,5-DHB 2,5-Dihydroxy benzoic acid, common matrix substance for MALDI MS analysis
MeCN, ACN acetonitrile, solvent
MeOH methanol, solvent
MeNO2 nitromethane, solvent
HABA 2-(4-hydroxyphenyl-azo)-benzoic acid, matrix substance for MALDI MS analysis
SA sinapic or sinapinic acid, common matrix substance for MALDI MS analysis
PEG Polyethylene glycol, Repeat unit: -[O-CH2-CH2-]-; 44 Da
PPG Polypropylene glycol, Repeat unit: -[O-C(CH3)H-CH2-]-; 58 Da
XaaCcamXaa carbamidomethylated cysteine residue (+ICH2CONH2 - HI), +57Da
XaaMoxXaa singly oxidized methionine residue (+O, 16 Da)

References

The data in these tables are primarily from:

  • the Supplementary Data from: Keller BO, Sui J, Young AB, Whittal RM. Interferences and contaminants encountered in modern mass spectrometry. Anal Chim Acta. 2008;627(1):71-81.

In the tables each entry references refers to the following table:

Ref Author(s) Citation or Website
A Waters Corporation Background Ion List
B Applied Biosystems Appendix D: Commonly Observed Background Ions — Mariner Biospectrometry Workstation Users Guide
C New Objective Common Background Ions for Electrospray (Technical Note)
D Sigma-Aldrich Chemical formulas for Tween, Triton, and reduced Triton from the Sigma-Aldrich catalogue
E Thermo Corporation; Mahn, B. List of LC/MS contaminants
F Tong, H.; Bell, D.; Tabei, K.; Siegel, M. M. J. Am. Soc. Mass Spectrom., 10 (1999) 1174
G Andersen, J. S.; Kuester, B.; Podtelejnikov, A.; Mortz, E.; Mann, M. Proc. 47th ASMS Conf. Mass Spectrom. Allied Topics, 1999, Dallas, TX
H Keller, B. O.; Li, L. J. Am. Soc. Mass Spectrom., 11 (2000) 88
I Keller, B. O.; Li, L.; Keller, H. MaClust: matrix cluster mass prediction
J Harris, W. A.; Janecki, D. J.; Reilly, J. P. Rapid Commun. Mass Spectrom., 16 (2002) 1714
K Keller, B. O.; Sui, J.; Young, A. B.; Whittal, R. M. Unpublished results; ESI background ions — Tween, Triton, PEGs, PPGs
L Schlosser, A.; Volkmer-Engert, R. J. Mass Spectrom., 38 (2003) 523
M Tran, J. C.; Doucette, A. A. J. Am. Soc. Mass Spectrom., 17 (2006) 652
N Verge, K. M.; Agnes, G. R. J. Am. Soc. Mass Spectrom., 13 (2002) 901
O Paez, A.; Howe, A. Canadian Chemical News, 56 (2004) 14
P Purves, R. W.; Gabryelski, W.; Li, L. Rev. Sci. Instrum., 68 (1997) 3252
Q Gibson, C. R.; Brown, C. M. J. Am. Soc. Mass Spectrom., 14 (2003) 1247
R Beavis, R. C.; Chait, B. T. Anal. Chem., 62 (1990) 1836
S Guzzetta, A. ionsource.com — Carbohydrate marker ions
T Clauser, K. R.; Hall, S. C.; Smith, D. M.; Webb, J. W.; Andrews, L. E.; Tran, H. M.; Epstein, L. B.; Burlingame, A. L. Proc. Natl. Acad. Sci. USA, 92 (1995) 5072; prospector.ucsf.edu
U Macha, S. F.; Limbach, P. A.; Hanton, S. D.; Owens, K. G. J. Am. Soc. Mass Spectrom., 12 (2001) 732
V Pleasance, S.; Thibault, P.; Sim, P. G.; Boyd, R. K. Rapid Commun. Mass Spectrom., 5 (1991) 307
W Xia, Y.; Patel, S.; Bakhtiar, R.; Franklin, R. B.; Doss, G. A. J. Am. Soc. Mass Spectrom., 16 (2005) 417
X Guo, X.; Bruins, A. P.; Covey, T. R. Rapid Commun. Mass Spectrom., 20 (2006) 3145
Y Ijames, C. F.; Dutky, R. C.; Fales, H. M. J. Am. Soc. Mass Spectrom., 6 (1995) 1226
Z Hesse, M.; Meier, H.; Zeeh, B. Spektroskopische Methoden in der organischen Chemie, Georg Thieme Verlag, Stuttgart, 3rd ed. 1987, ISBN: 3-13-576103-7
AA Stanstrup, J.

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A collection of common mz values found in mass spectrometry.

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