Accessing Intracellular Targets throuch Nanocarrier-Mediated Cytosolic Protein Delivery

被引:36
|
作者
Goswami, Ritabrita [1 ]
Jeon, Taewon [1 ,2 ]
Nagaraj, Harini [1 ]
Zhai, Shumei [3 ]
Rotello, Vincent M. [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[2] Univ Massachusetts, Mol & Cellular Biol Grad Program, Amherst, MA 01003 USA
[3] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Shandong, Peoples R China
关键词
CELL-PENETRATING PEPTIDES; FUSOGENIC LIPOSOMES; TECHNOLOGY EVALUATION; ENDOSOMAL ESCAPE; POLYMER; NANOPARTICLES; THERAPEUTICS; TRAFFICKING; DESIGN;
D O I
10.1016/j.tips.2020.08.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein-based therapeutics have unique therapeutic potential due to their specificity, potency, and low toxicity. The vast majority of intracellular applications of proteins require access to the cytosol. Direct entry to the cytosol is challenging due to the impermeability of the cell membrane to proteins. As a result, multiple strategies have focused on endocytic uptake of proteins. Endosomally entrapped cargo, however, can have very low escape efficiency, with protein degradation occurring in acidic endolysosomal compartments. In this review, we briefly discuss endosomal escape strategies and review the strategy of cell membrane fusion, a recent strategy for direct delivery of proteins into the cell cytoplasm.
引用
收藏
页码:743 / 754
页数:12
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