4.7 Article

One-step self-assembly of quantum dot-based spherical nucleic acid nanostructure for accurate monitoring of long noncoding RNA MALAT1 in living cells and tissues

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 469, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.144021

Keywords

Long non-coding RNA; Quantum dot; Spherical nucleic acid nanostructure; Forster resonance energy transfer

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In this study, a simple and sensitive measurement method for long non-coding RNA (lncRNA) was developed using self-assembled quantum dot (QD)-based spherical nucleic acid (SNA) nanostructures. The QD nanosensor achieved high sensitivity and accurate quantification of lncRNA expression, and it could differentiate tumor cells from normal cells and distinguish breast cancer patients from healthy individuals. This versatile paradigm provides a promising tool for biomedical research and early clinic diagnostics.
Simple and sensitive measurement of long non-coding RNA (lncRNA) is critical for early detection of malignancies. Herein, we demonstrate one-step self-assembly of quantum dot (QD)-based spherical nucleic acid (SNA) nanostructure for accurate monitoring of lncRNAs in living cells and tissues. When target lncRNA is present, it binds with a dumbbell probe to expose the complementary domain of Cy5-labeled primer, which subsequently induces cascade primer exchange reaction to produce abundant Cy5-labeled initiators. The Cy5-labeled initiators subsequently hybridize with hairpin probes on the QD surface to activate isothermal circular strand-displacement polymerization reaction, generating the QD-DNA-Cy5 nanostructures and inducing efficient Forster resonance energy transfer (FRET) between donor QD and acceptor Cy5. The obtained FRET signals are accurately quantified by single-molecule imaging. Notably, the single QD-based SNA nanostructure functions not only as a signal transmitter but also as a protector against non-specific amplification. Moreover, this assay utilizes only one DNA polymerase to achieve two-stage amplification, avoiding careful modulation of multiple enzymes. The self-assembly of QD nanosensor can be accomplished in single-step and single-tube manners at room temperature, eliminating precise temperature control and labor-intensive reaction protocols. This QD nanosensor achieves high sensitivity with a limit of detection (LOD) of 65.25 aM, and it is capable of quantifying lncRNA expression at single-cell level, differentiate tumor cells from normal cells, and distinguish breast cancer patients from healthy individuals, providing a versatile paradigm for biomedical research and early clinic diagnostics.

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