Skip to main navigation Skip to search Skip to main content

Intact glycopeptide characterization using mass spectrometry

  • Li Cao
  • , Yi Qu
  • , Zhaorui Zhang
  • , Zhe Wang
  • , Iya Prytkova
  • , Si Wu

Research output: Contribution to journalReview articlepeer-review

63 Scopus citations

Abstract

ABSTRACT: Glycosylation is one of the most prominent and extensively studied protein post-translational modifications. However, traditional proteomic studies at the peptide level (bottom-up) rarely characterize intact glycopeptides (glycosylated peptides without removing glycans), so no glycoprotein heterogeneity information is retained. Intact glycopeptide characterization, on the other hand, provides opportunities to simultaneously elucidate the glycan structure and the glycosylation site needed to reveal the actual biological function of protein glycosylation. Recently, significant improvements have been made in the characterization of intact glycopeptides, ranging from enrichment and separation, mass spectroscopy (MS) detection, to bioinformatics analysis. In this review, we recapitulated currently available intact glycopeptide characterization methods with respect to their advantages and limitations as well as their potential applications.

Original languageEnglish
Pages (from-to)513-522
Number of pages10
JournalExpert Review of Proteomics
Volume13
Issue number5
DOIs
StatePublished - 3 May 2016
Externally publishedYes

Keywords

  • Glycosylation
  • LC-MS/MS
  • bioinformatics
  • glycopeptide
  • post-translational modification
  • proteomics

Fingerprint

Dive into the research topics of 'Intact glycopeptide characterization using mass spectrometry'. Together they form a unique fingerprint.

Cite this