Sun Zixin, Chen Xiaohui, Niu Ruyan, Chen Hengyi, Zhu Ying, Zhang Chong, Wang Liu, Mou Huaming, Zhang Hong, Luo Yang
Department of Center of Smart Laboratory and Molecular Medicine, School of Medicine, Chongqing University, Chongqing, 400044, PR China.
Sanxia Hospital, Chongqing University, Chongqing, 404100, PR China.
Mater Today Bio. 2023 Mar 20;19:100613. doi: 10.1016/j.mtbio.2023.100613. eCollection 2023 Apr.
Accurate determination of single exosomal inclusions presents a significant challenge due to their extremely low abundance as well sub-100 nm vesicle dimensions. Here, we created a posome usogenic nzyme-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 . 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.
由于单个外泌体所含物质的丰度极低且囊泡尺寸小于100纳米,准确测定单个外泌体的内含物是一项重大挑战。在此,我们创建了一种基于正体的无酶循环(LIFE)方法,用于在不破坏囊泡完整性的情况下高保真鉴定外泌体包裹的货物。装载探针的阳离子融合脂质体可以捕获单个目标外泌体并与之融合,实现探针递送以及目标生物分子引发的级联信号放大。然后,DNAzyme探针在外泌体微小RNA激活后发生构象变化,形成凸形DNAzyme结构以切割底物探针的RNA位点。之后,目标微小RNA可被释放,引发切割循环以产生放大的荧光读数。因此,通过精心控制引入的LIFE探针比例,可以准确测定单个外泌体中的微量货物,为探索用于评估外泌体货物的通用传感平台铺平道路,以促进早期疾病诊断和个性化治疗。