MALDI-TOF mass spectrometry: a powerful tool to study the internalization of cell-penetrating peptides

Biochim Biophys Acta. 2010 Dec;1798(12):2182-9. doi: 10.1016/j.bbamem.2009.11.011. Epub 2009 Nov 22.

Abstract

This review summarizes the contribution of MALDI-TOF mass spectrometry in the study of cell-penetrating peptide (CPP) internalization in eukaryote cells. This technique was used to measure the efficiency of cell-penetrating peptide cellular uptake and cargo delivery and to analyze carrier and cargo intracellular degradation. The impact of thiol-containing membrane proteins on the internalization of CPP-cargo disulfide conjugates was also evaluated by combining MALDI-TOF MS with simple thiol-specific reactions. This highlighted the formation of cross-linked species to cell-surface proteins that either remained trapped in the cell membrane or led to intracellular delivery. MALDI-TOF MS is thus a powerful tool to dissect CPP internalization mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Membrane / chemistry*
  • Cell Membrane / metabolism
  • Cell-Penetrating Peptides / analysis*
  • Cell-Penetrating Peptides / chemistry
  • Cell-Penetrating Peptides / metabolism
  • Cell-Penetrating Peptides / pharmacology
  • Cross-Linking Reagents / analysis
  • Cross-Linking Reagents / chemistry
  • Humans
  • Membrane Proteins / analysis*
  • Membrane Proteins / chemistry
  • Membrane Proteins / metabolism
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods*
  • Sulfhydryl Compounds / metabolism

Substances

  • Cell-Penetrating Peptides
  • Cross-Linking Reagents
  • Membrane Proteins
  • Sulfhydryl Compounds