Nucleic acid-mediated intracellular protein delivery by lipid-like nanoparticles

被引:38
作者
Eltoukhy, Ahmed A. [1 ,2 ]
Chen, Delai [2 ]
Veiseh, Omid [2 ]
Pelet, Jeisa M. [2 ]
Yin, Hao [2 ]
Dong, Yizhou [2 ]
Anderson, Daniel G. [2 ,3 ,4 ,5 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] MIT, Inst Med Engn & Sci, Cambridge, MA 02139 USA
[5] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
Protein delivery; Nucleic acid; Oligonucleotide; Intracellular delivery; Nanoparticles; Lipid; CELL-PENETRATING PEPTIDES; VACCINE-DELIVERY; MAMMALIAN-CELLS; THERAPEUTICS; NANOCARRIERS; TRANSDUCTION; MECHANISMS; ADJUVANTS; VECTORS; SYSTEM;
D O I
10.1016/j.biomaterials.2014.04.014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Intracellular protein delivery has potential biotechnological and therapeutic application, but remains technically challenging. In contrast, a plethora of nucleic acid carriers have been developed, with lipid-based nanoparticles (LNPs) among the most clinically advanced reagents for oligonucleotide delivery. Here, we validate the hypothesis that oligonucleotides can serve as packaging materials to facilitate protein entrapment within and intracellular delivery by LNPs. Using two distinct model proteins, horseradish peroxidase and NeutrAvidin, we demonstrate that LNPs can yield efficient intracellular protein delivery in vitro when one or more oligonucleotides have been conjugated to the protein cargo. Moreover, in experiments with NeutrAvidin in vivo, we show that oligonucleotide conjugation significantly enhances LNP-mediated protein uptake within various spleen cell populations, suggesting that this approach may be particularly suitable for improved delivery of protein-based vaccines to antigen-presenting cells. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6454 / 6461
页数:8
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