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Simultaneous Analysis of Phosphorylated Peptides by MALDI-TOF-MS.

Authors :
Kang, J.
Toita, R.
Jiang, Y.
Niidome, T.
Katayama, Y.
Source :
Chromatographia; Jun2006, Vol. 63 Issue 11/12, p595-598, 4p
Publication Year :
2006

Abstract

Six peptides with various phosphorylation sensitivities for protein kinase A (PKA) were used for the simultaneous analysis of phosphorylated peptides using matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF) mass spectrometry. The mixture of six peptides was reacted with PKA and was analyzed by MALDI-TOF mass spectrometry. The intensity of all peaks except one phosphorylated peptide peak was very low (<20%). Moreover, we examined whether the addition of diammonium citrate to CHCA matrix at concentrations of 1–20 mg mL<superscript>−1</superscript> can increase the peak intensity of peptides and phosphorylated peptides. The addition of diammonium citrate increased the peak intensity of peptides and phosphorylated peptides, but an increase in the intensity was unsatisfactory. Our study strongly suggests that MALDI-TOF mass spectrometry is not suitable for the simultaneous analysis of phosphorylated peptides. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00095893
Volume :
63
Issue :
11/12
Database :
Complementary Index
Journal :
Chromatographia
Publication Type :
Academic Journal
Accession number :
49522977
Full Text :
https://doi.org/10.1365/s10337-006-0810-1