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

被引:30
作者
Aubry, Soline
Aussedat, Baptiste
Delaroche, Diane
Jiao, Chen-Yu
Bolbach, Gerard
Lavielle, Solange
Chassaing, Gerard
Sagan, Sandrine
Burlina, Fabienne [1 ]
机构
[1] Univ Paris 06, UPMC CNRS ENS Paris06, Lab BioMol, F-75005 Paris, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2010年 / 1798卷 / 12期
关键词
Cell-penetrating peptide; Drug delivery; MALDI-TOF MS; Internalization efficiency; Intracellular degradation; Thiol/disulfide exchanges; CARGO DELIVERY; DISULFIDE BONDS; TROJAN CARRIERS; IN-VITRO; QUANTIFICATION; STABILITY; ENTRY; MACROPINOCYTOSIS; TRANSDUCTION; INHIBITORS;
D O I
10.1016/j.bbamem.2009.11.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2182 / 2189
页数:8
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