Mercury ion–DNA specificity triggers a distinctive photoluminescence depression in organic semiconductor probes guided with a thymine-rich oligonucleotide sequence. Issue 37 (14th September 2018)

• Record Type: Journal Article
• Authors: Huang, Jietao; Park, Jin Hyuk; Back, Seung Hyuk; Feng, Yuhui; Cui, Chunzhi; Jin, Long Yi; Ahn, Dong June
• Is Part Of: Nanoscale. Volume 10:Issue 37(2018)
• Page Start: 17540
• Page End: 17545
• Publication Date: 2018-09-14
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c8nr03879a
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : An organic semiconductor particle triggers a "distinctive depressed luminescence" when crystallized with thymine-rich DNA strands having motifs forming a quadruplex conformation upon specific interaction with mercury. Abstract : DNA strands have been recently found to play a role in crystallizing organic semiconductors as a substitute for conventional surfactants. Such DNA-guided organic semiconductor particles possessed the recognition ability to complementary target DNAs, resulting in "enhanced luminescence" due to the lesser degree of non-radiative dissipation. Apart from this, in this study we developed selective recognition of mercury ions by utilizing DNA probes having ion-specific thymine-rich motifs. Strikingly, the specific ion–DNA interaction triggered rather distinctive "depressed luminescence" emitting from the particles. The mercury ions were found to be present both at the surface and the inner regions, which were discovered to relate to the drastic morphological distortion of the particles as evidenced by elemental, electron microscopy, and confocal fluorescence microscopy analyses. This novel phenomenon discovered would expand the technological values of organic semiconductors conjugated with oligonucleotides toward a wider range of target-specific applications.