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J Proteome Res. 2008 Mar;7(3):1001-6. doi: 10.1021/pr0705338. Epub 2008 Jan 26.

Identification and validation of eukaryotic aspartate and glutamate methylation in proteins.

Author information

1
Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9038, USA.

Abstract

Methylation of lysine and arginine is known to be critical in cellular processes. However, methylation of other amino acidic residues has been largely overlooked. Here, we report a systematic screening for methylation of side chains of aspartate and glutamate (D/E-methylation), involving exhaustive nano-HPLC/MS/MS, a protein sequence database search, and manual verification. The putative D/E-methylated peptides were confirmed by MS/MS of synthetic peptides. Our analysis identified several D/E-methylation substrate proteins and their modification sites in human and yeast cells. To our knowledge, this is the first report conclusively identifying in vivo D/E-methylation substrates and their modification sites in eukaryotic cells, demonstrating that D/E-methylations are abundant protein modifications. The substrate proteins identified here provide a stepping stone for future biochemical characterization of protein methylation pathways.

PMID:
18220335
PMCID:
PMC2921173
DOI:
10.1021/pr0705338
[Indexed for MEDLINE]
Free PMC Article

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