Complexes of DNA with cationic peptides: Conditions of formation and factors effecting internalization by mammalian cells

被引:15
作者
Dizhe, E. B.
Ignatovich, I. A.
Burov, S. V.
Pohvoscheva, A. V.
Akifiev, B. N.
Efremov, A. M.
Perevozchikov, A. P.
Orlov, S. V.
机构
[1] Russian Acad Med Sci, Inst Expt Med, St Petersburg 197376, Russia
[2] Russian Acad Sci, Inst Macromol Cpds, St Petersburg 199004, Russia
[3] St Petersburg State Univ, St Petersburg 199034, Russia
基金
俄罗斯基础研究基金会;
关键词
non-viral gene transfer approaches; cationic peptides; endocytosis; K8; Tat peptide;
D O I
10.1134/S0006297906120108
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 work was devoted to the study of conditions of the formation of DNA/K8 complex and analysis of factors effecting the entry of DNA/K8 complex into mammalian cells in comparison with DNA complexes with arginine-rich fragment (47-57) of human immunodeficiency virus (type 1) transcription factor Tat (Tat peptide). The stoichiometry of positively charged DNA/K8 complexes has been studied for the first time. Non-cooperative character of DNA-K8 interaction was revealed. It has been shown that along with the positive charge of such complexes, the presence of an excess of free K8 peptide in the culture medium is a necessary condition for maximal efficiency of cell transfection with DNA/K8 complexes. A stimulatory effect of free K8 peptide on the efficiency of mammalian cell transfection by DNA/K8 complexes is likely to be mediated by the interactions of cationic peptide K8 with negatively charged proteoglycans on the cell surface, which leads to protection of DNA/K8 complexes from disruption by cellular heparan sulfates. However, the protective role of free cationic peptides depends not only on their positive charge, but also on the primary structure of the peptide. In contrast with the results obtained for DNA complexes with molecular conjugates based on poly-L-lysine, the aggregation of DNA/K8 complexes leads to a significant increase in the expression of transferred gene.
引用
收藏
页码:1350 / 1356
页数:7
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