RESUMEN
The development of a simple and effective method for the highly sensitive and selective discrimination of proteins is a subject of enormous interest. Herein, we report the construction of a novel fluorescence detection method based on a perylene probe for the highly efficient discrimination of multiple proteins. Single-stranded DNA (ssDNA) could induce aggregation of the perylene probe which caused quenching of probe fluorescence. After the addition of a protein, the protein could interact with the ssDNA-probe assembly complex with "turn-on" or further "turn-off" fluorescence response. A sensor array was designed based on the above phenomena which could realize the successful discrimination of proteins with 100% accuracy of cross validation. Nine representative proteins were successfully recognized. Moreover, it was observed that a protein could induce characteristic effect on the DNA-probe assembly with varying pH of assay buffer. Thus, different proteins showed unique fluorescence response towards assay buffers having different pH values. The assay buffer pH was then utilized as a sensing channel. Based on Linear Discriminant Analysis (LDA) nine proteins were successfully discriminated at the nanomolar concentration with 100% accuracy of cross validation. Furthermore, the sensor array also demonstrated differentiation of the nine proteins regardless of their concentration. The developed sensor array could also detect the proteins with great precision in human urine sample at a quite low concentration, which suggests its practical applicability for analysis of biological fluids.
Asunto(s)
Perileno , ADN/genética , ADN de Cadena Simple , Colorantes Fluorescentes , Humanos , Proteínas , Espectrometría de FluorescenciaRESUMEN
A hydroxyl functionalized perylene monoimide probe (PMI-OH) was prepared and self-assembled with the nonionic surfactant Triton X-100 (TX100) to fabricate a fluorescent micelle sensor for the selective and sensitive detection of picric acid (PA), a common explosive and environmental pollutant. The synthesized PMI-OH probe exhibited excimer fluorescence emission, and the intensity of the excimer fluorescence emission was significantly enhanced after the PMI-OH probe formed micelles with TX100. The obtained PMI-OH@TX100 micelles presented excellent photoluminescence properties and had a maximum fluorescence emission at 630 nm. The red fluorescence of the PMI-OH@TX100 micelles was quenched upon introduction of the nitro explosive PA due to electron transfer from the donor (PMI-OH) to the acceptor (PA). The fluorescence quenching of the fluorescent micelle sensor was proportional to the concentration of PA in the range of 2 to 10 µM. The limit of detection was 500 nM using 3σ/k. Thus, the developed PMI-OH@TX100 micelle sensor has great potential to detect PA in ordinary samples.
RESUMEN
Diabetes is a rapidly growing disease that can be monitored at an individual level by controlling the blood glucose level, hence minimizing the negative impact of the disease. Significant research efforts have been focused on the design of novel and improved technologies to overcome the limitations of existing glucose analysis methods. In this context, nanotechnology has enabled the diagnosis at the single cell and molecular level with the possibility of incorporation in advanced molecular diagnostic biochips. Recent years have witnessed the exploration and synthesis of various types of nanomaterials with enzyme-like properties, with their subsequent integration into the design of biomimetic optical sensors for glucose monitoring. This review paper will provide insights on the type, nature and synthesis of different biomimetic nanomaterials. Moreover, recent developments in the integration of these nanomaterials for optical glucose biosensing will be highlighted, with a final discussion on the challenges that must be addressed for successful implementation of these nano-devices in the clinical applications is presented.