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This protocol describes a high-throughput screening system that uses fluorescence polarization of a specific fluorescent probe binding to a nuclear receptor as a readout for screening environmental pollutants.
Increasing levels of compounds have been detected in the environment, causing widespread pollution and posing risks to human health. However, despite their high environmental occurrence, there is very limited information regarding their toxicological effects. It is urgent to develop high-throughput screening (HTS) methods to guide toxicological studies. In this study, a receptor-ligand binding assay using an HTS system was developed to determine the binding potency of environmental pollutants on nuclear receptors. The test is conducted using a microplate reader (i.e., a 96-well plate containing various chemicals) by measuring the fluorescence polarization (FP) of a specific fluorescent probe. This assay consists of four parts: the construction and transformation of recombinant vectors, the expression and purification of the receptor protein (ligand-binding domain), receptor-probe binding, and competitive binding of chemicals with the receptor. The binding potency of two environmental pollutants, perfluorooctanesulfonic acid (PFOS) and triphenyl phosphate (TPHP), with peroxisome proliferator-activated receptor gamma (PPARĪ³) was determined to illustrate the assay procedure. Finally, the advantages and disadvantages of this method and its potential applications were also discussed.
A large number of chemicals have been widely detected in the environment and human bodies, raising significant concerns about their impact on the ecological environment and human health1,2,3. Despite their high environmental occurrence, information regarding their toxicological effects is scarce. Therefore, it is urgent to develop high-throughput screening (HTS) methods to facilitate the assessment of chemical toxicity.
Several high-throughput screening (HTS) methods have been reported for chemical toxicity assessment, such as the HTS bioassays use....
The details of the reagents and the equipment are listed in the Table of Materials.
1. Construction and transformation of recombinant vectors
NOTE: PPARĪ³ is a ligand-dependent transcription factor with a classical nuclear receptor structure, comprising a DNA-binding domain that regulates target genes and a ligand-binding domain activated by ligands. Upon ligand activation, PPARĪ³ forms a heterodimer with another nuclear recep.......
Protein expression and purification of PPARĪ³-LBD
PPARĪ³-LBD was heterologously expressed in BL21 (DE3) as a histidine-tagged protein. The protein was detected in the soluble fractions, and the purified PPARĪ³-LBD showed a single band on SDS-PAGE with an apparent molecular weight of approximately 34.9 kDa (Figure 2), consistent with the predicted molecular weight of the protein.
The binding of C1-BODIPY-C1.......
Fluorescence polarization (FP), surface plasmon resonance (SPR), and nuclear magnetic resonance (NMR) are common techniques used for assessing direct binding interactions between proteins and compounds19,20. FP has been widely employed in the investigation of molecular interactions for drug discovery and chemical screening21,22,23. In comparison, SPR and NMR assays are e.......
This work was supported by the National Natural Science Foundation of China (Grant No. 82103875).
....Name | Company | Catalog Number | Comments |
C1-BODIPY-C12 Probe | Thermo Fisher Scientific, China | 102209-82-3 | Binds to PPARĪ³-LBD and emits fluorescence. |
Coomassie Brilliant Blue R-250 | Solarbio, China | 6104-59-2 | Stain the protein bands. |
GraphPad prism | Dotmatics | https://www.graphpad.com/features | |
imidazole | Solarbio, China | I8090 | Prepare buffers for the protein purification process. |
Isopropyl Ī²-D-1-thiogalactopyranoside | Solarbio, China | 367-93-1 | Induce the expression of PPARĪ³-LBD |
Microplate reader | Biotek , USA | Synergy H1Ā | Detecting FP value |
NaCl | Shanghai Reagent | 7647-15-5 | Prepare buffers for the protein purification process. |
NaH2PO4 Ā· 2H2O | Shanghai Reagent | 13472-35-0 | Prepare buffers for the protein purification process. |
Ni NTA Beads 6FF | Smart-Lifesciences, China | SA005005 | Protein purification. |
Origin 8.5Ā | OriginLab, Northampton, MA, U.S.A. | ||
Perfluorooctanesulfonic acid (PFOS) | J&K Scientific Ltd, China | 1763-23-1 | The detected environmental pollutants |
Phenylmethylsulfonyl fluoride (PMSF) | Solarbio, China | P0100 | Inhibit protein degradation. |
PPARĪ³-Competitor Assay Kit | Thermo Fisher Scientific | PV6136 | https://www.thermofisher.com/order/catalog/product/PV6136 |
PPARĪ³-LBD Ligand Screening Assay Kit | Cayman | 600616 | https://www.caymanchem.com/product/600616 |
Rosiglitazone (Rosi) | aladdin, China | 122320-73-4 | The agonists of PPARĪ³ |
Shaker | ZHICHENG, China | ZWY-211C | Bacterial culture expansion and induction of protein expression |
Triphenyl phosphate (TPHP) | Macklin, China | T819317 | The detected environmental pollutants |
Tris | Solarbio, China | T8230 | Prepare buffers for the protein purification process. |
Tryptone | OXOID Limited, China | LP0042B | Prepare Lysogeny Broth (LB) medium. |
Ultrasonic Cleaner | Kimberly, China | LHO-1 | Disrupt the bacteria to achieve complete lysis |
Urea | Solarbio, China | U8020 | Prepare buffers for the protein purification process. |
Yeast extract | OXOID Limited, China | LP0021B | Prepare Lysogeny Broth (LB) medium. |
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