On-site monitoring of trace organic
pollutants with facile methods
is critical to environmental pollutant prevention and control. Herein,
we proposed a CRISPR-Cas12a-based aptasensor platform (named as MC-LR-Casor)
for on-site and sensitive detection of microcystin-LR (MC-LR). After
hybridization with blocker DNA, the MC-LR aptamers were conjugated
to magnetic beads (MBs) to get the MB aptasensor. In the presence
of MC-LR, their interactions with aptamers were triggered and the
specific binding caused the release of blocker DNA. Using the programmability
of the CRISPR-Cas system, the released blocker DNA was designed to
activate a Cas12a-crRNA complex. Single strand DNA reporters were
rapidly cleaved by the complex. Signal readout could be achieved by
fluorometer or lateral flow strips, which were positively correlated
to MC-LR concentration. Benefiting from the CRISPR-Cas12a amplification
system, the proposed sensing platform exhibited high sensitivity and
reached the limit of detection of ∼3 × 10–6 μg/L (fluorescence method) or 1 × 10–3 μg/L (lateral flow assay). In addition, the MC-LR-Casor showed
excellent selectivity and good recovery rates, demonstrating their
good applicability for real water sample analysis. During the whole
assay, only two steps of incubation at a constant temperature were
required and the results could be visualized when employing flow strips.
Therefore, the proposed assay offered a simple and convenient alternative
for in situ MC-LR monitoring, which may hold great promise for future
environmental surveillance.
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