posted on 2021-01-06, 15:41authored byTuli Kang, Jingtian Zhu, Xiaojun Luo, Wenyu Jia, Ping Wu, Chenxin Cai
MicroRNAs
(miRNAs) in exosomes can be transferred from parental
cells to recipient cells by trafficking exosomes, and they are effective
in regulating the gene expression of the recipient cells. Therefore,
exosomal miRNAs play a vital role in cancer biology and could be potential
biomarkers for cancer diagnosis and therapeutic responses. However,
accurate detection of exosomal miRNAs is still challenging due to
the low abundance of any given miRNA in exosomes. Herein, a surface-enhanced
Raman scattering (SERS)-based sensor was developed for the quantitative
determination of let-7a miRNAs in MCF-7 cell-derived exosomes (MCF-7
exosomes) using a close-packed and ordered Au octahedral array as
a sensing platform. Au octahedra in the array uniformly stand on their
triangular face. This kind of orientation produces “hot surfaces”
rather than “hot spots” and greatly improves the detection
sensitivity and uniformity. Let-7a detection with single-base specificity
was thus achieved from the SERS intensity change induced by the structural
switch of the probing DNA from a hairpin to a duplex in the presence
of the target. The sensor showed a broad linear range (10 aM to 10
nM) and a low detection limit (5.3 aM) without using any signal amplification
strategy. Moreover, this sensor could accurately detect target let-7a
in MCF-7 exosomes and further value the impact of drug treatment on
exosomal let-7a expression, indicating promising applications of the
developed sensor for cancer diagnostics and therapy.