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Arginine-rich cross-linking peptides with different SV40 nuclear localization signal content as vectors for intranuclear DNA delivery
被引:21
作者:
Bogacheva, Mariia
[1
,2
]
Egorova, Anna
[1
]
Slita, Anna
[1
]
Maretina, Marianna
[1
]
Baranov, Vladislav
[1
]
Kiselev, Anton
[1
]
机构:
[1] DO Ott Res Inst Obstet Gynecol & Reproductol, Mendeleevskaya Line,3, St Petersburg 199034, Russia
[2] Univ Helsinki, Ctr Drug Res, Fac Pharm, POB 56, FI-00014 Helsinki, Finland
基金:
俄罗斯基础研究基金会;
俄罗斯科学基金会;
关键词:
SV40;
Nuclear localization signal;
Cross-linking peptides;
DNA;
Transfection;
Intranuclear delivery;
Non-viral vectors;
GENE DELIVERY;
PLASMID DNA;
TRANSFECTION EFFICIENCY;
SYSTEMS;
CELLS;
MICROINJECTION;
COMPLEXES;
HISTIDINE;
CARRIERS;
BINDING;
D O I:
10.1016/j.bmcl.2017.10.001
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
The major barriers for intracellular DNA transportation by cationic polymers are their toxicity, poor endosomal escape and inefficient nuclear uptake. Therefore, we designed novel modular peptide-based carriers modified with SV40 nuclear localization signal (NLS). Core peptide consists of arginine, histidine and cysteine residues for DNA condensation, endosomal escape promotion and interpeptide cross-linking, respectively. We investigated three polyplexes with different NLS content (10 mol%, 50 mol% and 90 mol% of SV40 NLS) as vectors for intranuclear DNA delivery. All carriers tested were able to condense DNA, to protect it from DNAase I and were not toxic to the cells. We observed that cell cycle arrest by hydroxyurea did not affect transfection efficacy of NLS-modified carriers which we confirmed using quantitative confocal microscopy analysis. Overall, peptide carrier modified with 90 mol% of SV40 NLS provided efficient transfection and nuclear uptake in non-dividing cells. Thus, incorporation of NLS into arginine-rich cross-linking peptides is an adequate approach to the development of efficient intranuclear gene delivery vehicles. (C) 2017 Elsevier Ltd. All rights reserved.
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页码:4781 / 4785
页数:5
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