Fabrication of an Aptamer-Coated Liposome Complex for the Detection and Profiling of Exosomes Based on Terminal Deoxynucleotidyl Transferase-Mediated Signal Amplification

被引:72
作者
Wang, Lei [1 ]
Pan, Yanhong [1 ]
Liu, Yunfei [1 ]
Sun, Zhaowei [1 ]
Huang, Yue [2 ]
Li, Jinlong [3 ]
Yang, Jie [1 ]
Xiang, Yang [1 ]
Li, Genxi [1 ,4 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Forestry Univ, Coll Light Ind & Food Engn, Dept Food Sci & Engn, Nanjing 210037, Peoples R China
[3] Nanjing Univ Chinese Med, Hosp Nanjing 2, Dept Lab Med, Nanjing 210003, Peoples R China
[4] Shanghai Univ, Ctr Mol Recognit & Biosensing, Sch Life Sci, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
aptamer-coated liposome; exosome profiling; heterogeneity; TdT; G-quadruplex; EXTRACELLULAR VESICLES;
D O I
10.1021/acsami.9b18869
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The exosome is a promising biomarker carrying many kinds of membrane proteins with huge heterogeneity, so the sensitive and multiplex analysis of exosomes is very significant for disease diagnosis and exploration of their biological functions. Herein, we propose an efficient method for highly sensitive detection and heterogeneity identification of exosomes based on the design and fabrication of an aptamer-coated liposome complex coupled with terminal deoxynucleotidyl transferase (TdT)-mediated polymerization. Specifically, in the presence of target exosomes, the aptamers immobilized on the surface of 1,2-dioleoyl-3-trimethylammonium-propane liposomes prefer to bind with exosomal membrane proteins due to the high affinity. The resulting aptamer-exosome complex will be accessible to TdT to switch on the polymerization reaction for signal amplification, achieving highly sensitive detection of exosomes. Furthermore, the proposed method can be employed to profile different exosomal membrane proteins by making use of a cluster of corresponding aptamers and obtain a fingerprint map of various cancer cell-derived exosomes. Thus, our approach may provide a highly sensitive and robust strategy for the identification of exosome heterogeneity with advantages of being label-free and having no separation, potentially enabling the precise subpopulation of exosomes with practical value in clinical applications.
引用
收藏
页码:322 / 329
页数:8
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