Differentiation between peptides containing acetylated or tri-methylated lysines by mass spectrometry: An application for determining lysine 9 acetylation and methylation of histone H3

Kangling Zhang, Peter M. Yau, Bhaskar Chandrasekhar, Ron New, Richard Kondrat, Brian S. Imai, Morton E. Bradbury

Research output: Contribution to journalArticle

115 Citations (Scopus)

Abstract

Histone acetylation and methylation play a critical role in transcription and gene regulation. Identification of sites of lysine acetylation and methylation in histones or other proteins by mass spectrometry (MS) is of increasing interest. In this paper, we report the use of MS to differentiate between peptides containing acetylated or tri-methylated lysines. High accuracy matrix-assisted laser desorption/ionization-time of flight MS gives better than five parts per million measurement accuracy, which is sufficient to verify acetylation and/or methylation. Electrospray ionization tandem mass spectrometry was used to assign modification sites and to differentiate acetylation from methylation. Typically, an immonium ion at m/z 98 corresponds to a mono-methylated lysine and an immonium ion at m/z 126 corresponds to an acetylated lysine. The neutral loss ion (MH+-59) is unique for a tri-methylated lysine. For a peptide with two or more modification sites of acetylation or tri-methylation or one site containing partial acetylation and tri-methylation, the a2-, b2-type ion is the characteristic index for an acetylated lysine whereas the b2-59 ion is indicative of a tri-methylated lysine in the N-terminus. The y-type ions and y-59 ions are charateristic of an acetylated lysine and a tri-methylated lysine at the C-terminus, respectively. We demonstrated that a lysine in a peptide modified by methylation or acetylation can be differentiated by MS using our method. Even if more then one lysine is present in a peptide and different modifications of this amino acid occur, they can be distinguished. This method was successful for the determination of the acetylation and methylation status of lysine 9 of histone H3 in chicken erythrocytes and human HeLa cell lines.

Original languageEnglish (US)
Pages (from-to)1-10
Number of pages10
JournalProteomics
Volume4
Issue number1
DOIs
StatePublished - Jan 2004
Externally publishedYes

Fingerprint

Acetylation
Methylation
Histones
Lysine
Mass spectrometry
Mass Spectrometry
Peptides
Ions
Electrospray ionization
Electrospray Ionization Mass Spectrometry
Transcription
Tandem Mass Spectrometry
HeLa Cells
Gene expression
Ionization
Chickens
Desorption
Lasers

Keywords

  • Histone acetylation
  • Histone methylation
  • Histones
  • Mass spectrometry

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

Differentiation between peptides containing acetylated or tri-methylated lysines by mass spectrometry : An application for determining lysine 9 acetylation and methylation of histone H3. / Zhang, Kangling; Yau, Peter M.; Chandrasekhar, Bhaskar; New, Ron; Kondrat, Richard; Imai, Brian S.; Bradbury, Morton E.

In: Proteomics, Vol. 4, No. 1, 01.2004, p. 1-10.

Research output: Contribution to journalArticle

Zhang, Kangling ; Yau, Peter M. ; Chandrasekhar, Bhaskar ; New, Ron ; Kondrat, Richard ; Imai, Brian S. ; Bradbury, Morton E. / Differentiation between peptides containing acetylated or tri-methylated lysines by mass spectrometry : An application for determining lysine 9 acetylation and methylation of histone H3. In: Proteomics. 2004 ; Vol. 4, No. 1. pp. 1-10.
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