| Literature DB >> 19932680 |
Soline Aubry1, Baptiste Aussedat, Diane Delaroche, Chen-Yu Jiao, Gérard Bolbach, Solange Lavielle, Gérard Chassaing, Sandrine Sagan, Fabienne Burlina.
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.Entities:
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Year: 2009 PMID: 19932680 DOI: 10.1016/j.bbamem.2009.11.011
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002