The
strategies for
nucleic acid sensing based on nucleic acid hybridization
between the target sequence and the capture probe sequence are considered
to be largely successful as far as detection of a specific target
of known sequence is concerned. However, when compared with other
complementary methods, like direct sequencing, a number of results
are still found to be either “false positives” or “false
negatives”. This suggests that modifications in these strategies
are necessary to make them more accurate. In this minireview, we propose
that one way toward improvement could be replacement of the DNA capture
probes with the xeno nucleic acid or XNA capture probes. This is because
the XNAs, especially the locked nucleic acid, the peptide nucleic
acid, and the morpholino, have shown better single nucleobase mismatch
discrimination capacity than the DNA capture probes, indicating their
capacity for more precise detection of nucleic acid sequences, which
is beneficial for detection of gene stretches having point mutations.
Keeping the current trend in mind, this minireview will include the
recent developments in nanoscale, fluorescent label-free applications,
and present the cases where the XNA probes show clear advantages over
the DNA probes.