Biomineralized Metal-Organic Framework Nanoparticles Enable Intracellular Delivery and Endo-Lysosomal Release of Native Active Proteins

被引:405
作者
Chen, Ting-Ting [1 ]
Yi, Jin-Tao [1 ]
Zhao, Yan-Yan [1 ]
Chu, Xia [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
ONE-POT SYNTHESIS; DE-NOVO APPROACH; LIVE CELLS; BIOMIMETIC MINERALIZATION; PHOTODYNAMIC THERAPY; EMBEDDING ENZYMES; CANCER-THERAPY; DRUG-DELIVERY; CO-DELIVERY; APOPTOSIS;
D O I
10.1021/jacs.8b04457
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Efficient delivery and endo-lysosomal release of active proteins in living cells remain a challenge in protein-based theranostics. We report a novel protein delivery platform using protein-encapsulating biomineralized metal organic framework (MOF) nanoparticles (NPs). This platform introduces an adapted biomimetic mineralization method for facile synthesis of MOF NPs with high protein encapsulation efficiency and a new polymer coating strategy to confer the NPs with long-term stability. In vitro results show that protein-encapsulating MOF NPs have the advantages of preserving protein activity for months and protecting proteins from enzyme-mediated degradation. Live cell studies reveal that MOF NPs enable rapid cellular uptake, efficient release and escape of proteins from endo-lysosomes, and preservation of protein activity in living cells. Moreover, the developed platform is demonstrated to enable easy encapsulation of multiple proteins in single MOF NPs for efficient protein co-delivery. To our knowledge, it is the first time that protein-encapsulating MOF NPs have been developed as a generally applicable strategy for intracellular delivery of native active proteins. The developed protein-encapsulating biomineralized MOF NPs can provide a valuable platform for protein-based theranostic applications.
引用
收藏
页码:9912 / 9920
页数:9
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