Integrating Protein Engineering and Bioorthogonal Click Conjugation for Extracellular Vesicle Modulation and Intracellular Delivery

被引:150
作者
Wang, Ming [1 ]
Altinoglu, Sarah [1 ]
Takeda, Yuji S. [1 ]
Xu, Qiaobing [1 ]
机构
[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
基金
美国国家科学基金会;
关键词
NEWLY SYNTHESIZED PROTEINS; CANCER-THERAPY; MAMMALIAN-CELLS; IN-VIVO; EXOSOMES; CHEMISTRY; MOUSE; NANOPARTICLES; SIRNA;
D O I
10.1371/journal.pone.0141860
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Exosomes are small, cell-secreted vesicles that transfer proteins and genetic information between cells. This intercellular transmission regulates many physiological and pathological processes. Therefore, exosomes have emerged as novel biomarkers for disease diagnosis and as nanocarriers for drug delivery. Here, we report an easy-to-adapt and highly versatile methodology to modulate exosome composition and conjugate exosomes for intracellular delivery. Our strategy combines the metabolic labeling of newly synthesized proteins or glycan/glycoproteins of exosome-secreting cells with active azides and bioorthogonal click conjugation to modify and functionalize the exosomes. The azide-integrated can be conjugated to a variety of small molecules and proteins and can efficiently deliver conjugates into cells. The metabolic engineering of exosomes diversifies the chemistry of exosomes and expands the functions that can be introduced into exosomes, providing novel, powerful tools to study the roles of exosomes in biology and expand the biomedical potential of exosomes.
引用
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页数:12
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