外体
脱氧核酶
生物物理学
核糖核酸
脂质体
小泡
劈开
生物分子
纳米技术
化学
微泡
寡核苷酸
细胞生物学
计算生物学
材料科学
生物
小RNA
生物化学
膜
酶
DNA
基因
作者
Zixin Sun,Xiaohong Chen,Ruyan Niu,Hengyi Chen,Ying Zhu,Chong Zhang,Liu Wang,Huaming Mou,Hong Zhang,Yang Luo
标识
DOI:10.1016/j.mtbio.2023.100613
摘要
Accurate determination of single exosomal inclusions in situ presents a significant challenge due to their extremely low abundance as well sub-100 nm vesicle dimensions. Here, we created a Liposome Fusogenic Enzyme-free circuit (LIFE) approach for the high-fidelity identification of exosome-encapsulated cargoes without destroying the vesicle integrity. The probe-loaded cationic fusogenic liposome could capture and fuse with a single target exosome, enabling probes delivery and target biomolecule-initiated cascaded signal amplification in situ. Then the DNAzyme probe encountered conformal change upon exosomal microRNA activation, and generated a convex DNAzyme structure to cleave the RNA site of substrate probe. After that, the target microRNA could be released to introduce a cleavage cycle to yield amplified fluorescence readout. Therefore, trace cargoes in a single exosome could be accurately determined by elaborately controlling the ratio of introduced LIFE probe, paving the way toward the exploration of a universal sensing platform for the assessment of exosomal cargoes to facilitate early disease diagnosis and personalized treatment.
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