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Liquid chromatography mass spectrometry modifications

Bean, M. F., Pallante-Morell, S. L., Dulik, D. M., and Fenselau, C. (1990). Protocol for liquid chromatography/mass spectrometry of glutathione conjugates using postcolumn solvent modification. Anal. Chem. 62 121-124. [Pg.186]

Lohmann, W., Hayen, H., and Karst, U., Covalent protein modification by reactive drug metabolites using online electrochemistry/liquid chromatography/mass spectrometry, Anal. Chem., 80 (24), 9714, 2008. [Pg.228]

Yan, B., Vallier-Douglass, J., Brady, L., Steen, S., Han, M. and Pace, D., et al. Analysis of post-translational modifications in recombinant monoclonal antibody IgCl by reversed-phase liquid chromatography/mass spectrometry. /. Chromatogr. 1164 153-161, 2007. [Pg.356]

Zhang, L., Freitas, MA., Wickham, J., Parthun, M.R., Klisovic, M.I., Marcucd, G. and Byrd, J.C. (2004) Differential expression of histone post-translational modifications in acute myeloid and chronic lymphocytic leukemia determined by high-pressure liquid chromatography and mass spectrometry. Journal of the American Society for Mass Spectrometry, 15, 77-86. [Pg.96]

D. Noort, E.R. Verheij, A.G. Hulst, L.P.A. De Jong and H.P. Benschop, Characterization of sulfur mustard induced structural modifications in human hemoglobin by liquid chromatography-tandem mass spectrometry, Chem. Res. Toxicol., 9, 781-787 (1996). [Pg.449]

Liquid chromatography coupled with tandem mass spectrometry (LC-MS/ MS) is the central method for identifying proteins with PTMs (187,188) due to its high sensitivity, its ability to identify the site, and its ability to quantify the relative changes in PTM occupancy at distinct sites (189), among others. However, PTM analysis presents a number of analytical challenges because most modifications are low-abundance and/or substoichiometric and some are labile during MS and MS/MS. [Pg.403]

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See also in sourсe #XX -- [ Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 , Pg.114 , Pg.115 ]



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