A novel fluorescent turn-on biosensor based on QDs@GSH-GO fluorescence resonance energy transfer for sensitive glutathione S-transferase sensing and cellular imaging

作者：Chang, Lifang; He, Xiwen; Chen, Langxing^*; Zhang, Yukui

来源：Nanoscale, 2017, 9(11): 3881-3888.

DOI：10.1039/c6nr09944k

• QUANTUM DOTS
• GRAPHENE OXIDE
• FRET
• NANOPARTICLES
• AFFINITY
• ARCHITECTURE
• RECOGNITION
• EFFICIENT
• EMISSION
• PROBES

A novel fluorescent turn-on biosensor based on fluorescence resonance energy transfer (FRET) from GSH functionalized Mn-doped ZnS QDs to graphene oxide (GO) was constructed to determine glutathione S-transferases (GSTs) in live cells and human urine. The QDs@GSH is adsorbed on the GO surface via hydrogen bonding interaction between the GSH on the surface of QDs@GSH and GO, and as a result, fluorescence quenching of the QDs@GSH takes place because of FRET. The FRET efficiency from QDs@GSH to GO was calculated to be 86.3%. However, in the presence of GSTs, the FRET process could be inhibited by the specific interaction between the GSH on the surface of QDs@GSH and GSTs, which would keep the QDs@GSH far away from the GO surface, leading to the recovery of the fluorescence. The proposed sensor exhibited high sensitivity, selectivity, and excellent specificity in the buffer, live cells and human urine for the detection of GSTs. Under the physiological conditions (pH 7.4), dissociation constants and the detection limit of GST and ATP6 V1F (a GST-tagged protein) were estimated to be 8.0 x 10(-9) M, 2.1 x 10(-10) M and 3.5 x 10(-9) M, 7.2 x 10(-11) M, respectively. The presented method has been successfully utilized for the determination of the GSTs in live cells and human urine without any complicated pretreatment and the recovery was in the range of 80%-90%.

• 出版日期2017-3-21
• 单位中国科学院; 南开大学; 中国科学院大连化学物理研究所; 药物化学生物学国家重点实验室