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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
AbbreviationsExplanation
4-HCCAα-cyano-4-hydroxycinnamic acid, common matrix substance for MALDI MS analysis
2,5-DHB2,5-Dihydroxy benzoic acid, common matrix substance for MALDI MS analysis
MeCN, ACNacetonitrile, solvent
MeOHmethanol, solvent
MeNO2nitromethane, solvent
HABA2-(4-hydroxyphenyl-azo)-benzoic acid, matrix substance for MALDI MS analysis
SAsinapic or sinapinic acid, common matrix substance for MALDI MS analysis
PEGPolyethylene glycol, Repeat unit: -[O-CH2-CH2-]-; 44 Da
PPGPolypropylene glycol, Repeat unit: -[O-C(CH3)H-CH2-]-; 58 Da
XaaCcamXaacarbamidomethylated cysteine residue (+ICH2CONH2 - HI), +57Da
XaaMoxXaasingly 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:

RefAuthor(s)Citation or Website
AWaters CorporationBackground Ion List
BApplied BiosystemsAppendix D: Commonly Observed Background Ions — Mariner Biospectrometry Workstation Users Guide
CNew ObjectiveCommon Background Ions for Electrospray (Technical Note)
DSigma-AldrichChemical formulas for Tween, Triton, and reduced Triton from the Sigma-Aldrich catalogue
EThermo Corporation; Mahn, B.List of LC/MS contaminants
FTong, H.; Bell, D.; Tabei, K.; Siegel, M. M.J. Am. Soc. Mass Spectrom., 10 (1999) 1174
GAndersen, J. S.; Kuester, B.; Podtelejnikov, A.; Mortz, E.; Mann, M.Proc. 47th ASMS Conf. Mass Spectrom. Allied Topics, 1999, Dallas, TX
HKeller, B. O.; Li, L.J. Am. Soc. Mass Spectrom., 11 (2000) 88
IKeller, B. O.; Li, L.; Keller, H.MaClust: matrix cluster mass prediction
JHarris, W. A.; Janecki, D. J.; Reilly, J. P.Rapid Commun. Mass Spectrom., 16 (2002) 1714
KKeller, B. O.; Sui, J.; Young, A. B.; Whittal, R. M.Unpublished results; ESI background ions — Tween, Triton, PEGs, PPGs
LSchlosser, A.; Volkmer-Engert, R.J. Mass Spectrom., 38 (2003) 523
MTran, J. C.; Doucette, A. A.J. Am. Soc. Mass Spectrom., 17 (2006) 652
NVerge, K. M.; Agnes, G. R.J. Am. Soc. Mass Spectrom., 13 (2002) 901
OPaez, A.; Howe, A.Canadian Chemical News, 56 (2004) 14
PPurves, R. W.; Gabryelski, W.; Li, L.Rev. Sci. Instrum., 68 (1997) 3252
QGibson, C. R.; Brown, C. M.J. Am. Soc. Mass Spectrom., 14 (2003) 1247
RBeavis, R. C.; Chait, B. T.Anal. Chem., 62 (1990) 1836
SGuzzetta, A.ionsource.com — Carbohydrate marker ions
TClauser, 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
UMacha, S. F.; Limbach, P. A.; Hanton, S. D.; Owens, K. G.J. Am. Soc. Mass Spectrom., 12 (2001) 732
VPleasance, S.; Thibault, P.; Sim, P. G.; Boyd, R. K.Rapid Commun. Mass Spectrom., 5 (1991) 307
WXia, Y.; Patel, S.; Bakhtiar, R.; Franklin, R. B.; Doss, G. A.J. Am. Soc. Mass Spectrom., 16 (2005) 417
XGuo, X.; Bruins, A. P.; Covey, T. R.Rapid Commun. Mass Spectrom., 20 (2006) 3145
YIjames, C. F.; Dutky, R. C.; Fales, H. M.J. Am. Soc. Mass Spectrom., 6 (1995) 1226
ZHesse, M.; Meier, H.; Zeeh, B.Spektroskopische Methoden in der organischen Chemie, Georg Thieme Verlag, Stuttgart, 3rd ed. 1987, ISBN: 3-13-576103-7
AAStanstrup, J.

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A collection of common mz values found in mass spectrometry.

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