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A PNA‐DNA 2 Triple‐Helix Molecular Switch‐Based Colorimetric Sensor for Sensitive and Specific Detection of microRNAs from Cancer Cells
Author(s) -
Xu Mengjia,
Fu Pan,
Xing Shu,
Zhao Yang,
Zhao Chao
Publication year - 2020
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.202000155
Subject(s) - dna , oligonucleotide , cyanine , peptide nucleic acid , nucleic acid , chemistry , triple helix , fluorescence , nucleic acid thermodynamics , biophysics , biochemistry , combinatorial chemistry , microbiology and biotechnology , biology , base sequence , stereochemistry , physics , quantum mechanics
Peptide nucleic acids (PNAs), the synthetic DNA mimics that can bind to oligonucleotides to form duplexes, triplexes, and quadruplexes, could be advantageous as probes for nucleic acid sequences owing to their unique physicochemical and biochemical properties. We have found that a homopurine PNA strand could bind to two homopyrimidine DNA strands to form a PNA‐DNA 2 triplex. Moreover, the cyanine dye DiSC 2 (5) could bind with high affinity to this triplex and cause a noticeable color change. On the basis of this phenomenon, we have designed a label‐free colorimetric sensing platform for miRNAs from cancer cells by using a PNA‐DNA 2 triple‐helix molecular switch (THMS) and DiSC 2 (5). This sensing platform can detect miRNA‐21 specifically with a detection limit of 0.18 nM, which is comparable to that of the THMS‐mediated fluorescence sensing platform. Moreover, this colorimetric platform does not involve any chemical modification or enzymatic signal amplification, which boosts its applicability and availability at the point of care in resource‐limited settings. The universality of this approach can be simply achieved by altering the sequences of the probe DNA for specific targets.