Details

Autor(en) / Beteiligte

• Lee, Junghan
• Kwon, Yong-Jun
• Choi, Youngseon
• Kim, Hi Chul
• Kim, Keumhyun
• Kim, JinYeop
• Park, Sun
• Song, Rita

Titel

Quantum Dot-Based Screening System for Discovery of G Protein-Coupled Receptor Agonists

Ist Teil von

• Chembiochem : a European journal of chemical biology, 2012-07, Vol.13 (10), p.1503-1508

Ort / Verlag

Weinheim: WILEY-VCH Verlag

Erscheinungsjahr

2012

Quelle

Wiley-Blackwell Full Collection

Beschreibungen/Notizen

• Cellular imaging has emerged as an important tool to unravel biological complexity and to accelerate the drug‐discovery process, including cell‐based screening, target identification, and mechanism of action studies. Recently, semiconductor nanoparticles known as quantum dots (QDs) have attracted great interest in cellular imaging applications due to their unique photophysical properties such as size, tunable optical property, multiplexing capability, and photostability. Herein, we show that QDs can also be applied to assay development and eventually to high‐throughput/content screening (HTS/HCS) for drug discovery. We have synthesized QDs modified with PEG and primary antibodies to be used as fluorescent probes for a cell‐based HTS system. The G protein‐coupled receptor (GPCR) family is known to be involved in most major diseases. We therefore constructed human osteosarcoma (U2OS) cells that specifically overexpress two types of differently tagged GPCRs: influenza hemagglutinin (HA) peptide‐tagged κ‐opioid receptors (κ‐ORs) and GFP‐tagged A3 adenosine receptors (A3AR). In this study, we have demonstrated that 1) anti‐HA antibody‐conjugated QDs could specifically label HA‐tagged κ‐ORs, 2) subsequent treatment of QD‐tagged GPCR agonists allowed agonist‐induced translocation to be monitored in real time, 3) excellent emission spectral properties of QD permitted the simultaneous detection of two GPCRs in one cell, and 4) the robust imaging capabilities of the QD–antibody conjugates could lead to reproducible quantitative data from high‐content cellular images. These results suggest that the present QD‐based GPCR inhibitor screening system can be a promising platform for further drug screening applications. Get real: Quantum dots (QDs) modified with PEG and antibodies were developed as fluorescent probes for cell‐based assays for GPCRs. We have demonstrated that anti‐hemagglutinin (HA) antibody‐conjugated QDs could specifically label HA‐tagged κ‐opioid receptors, and subsequent treatment with agonists could be used to monitor GPCR translocation in real time.