Etelka Kiss, Dávid Mester, Dóra Hessz, Ervin Kovács, Krisztina László, Miklós Kubinyi
For ATP detection, indicator displacement assays with multicationic macrocyclic hosts and anionic fluorescent dye guests represent an intuitive design strategy. However, such systems typically exhibit turn-off responses. For biological samples with strong background- and autofluorescence, ratiometric or turn-on signaling is preferred, which requires more sophisticated assay architectures. In the present work, the host-guest complexation of fluorescent pH indicator dye trisodium 8-hydroxypyrene-1,3,6-trisulfonic acid (HPTS) with a cationic ammonium-pillar[6]arene (AP6) was employed in the design of indicator displacement assays featuring two distinct detection modes for the fluorescent sensing of nucleotide ATP. In the first approach, AP6-assisted deprotonation of HPTS enabled the development of a colorimetric and a fluorescent ratiometric assay. In the second strategy, fluorescence turn-on sensing was achieved by exploiting the FRET-type quenching of HPTS fluorescence by AP6-modified reduced graphene oxide (rGO-AP6). Both sensing platforms demonstrated high selectivity toward ATP over structurally similar nucleotides and other biologically relevant anions, a broad dynamic range and a low limit of detection. The performance of the turn-on ATP sensor was validated in the complex biological matrix of human serum, demonstrating its applicability for practical bioanalytical applications.