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Cited 7 time in webofscience Cited 8 time in scopus
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Rapid Screening of Glucocorticoid Receptor (GR) Effectors Using Cortisol-Detecting Sensor Cellsopen access

Authors
Ryu, JeaheeLee, EuiyeonKang, ChungwonLee, MinhyeongKim, SoyounPark, SeungilLee, DaeyeonKwon, Youngeun
Issue Date
May-2021
Publisher
MDPI
Keywords
cortisol; glucocorticoid receptor (GR); GR effector; selective GR agonist; cell-based sensor; signal peptide reconstitution; conditional protein splicing
Citation
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.9
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume
22
Number
9
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/5036
DOI
10.3390/ijms22094747
ISSN
1661-6596
1422-0067
Abstract
Cortisol, a stress hormone, plays key roles in mediating stress and anti-inflammatory responses. As abnormal cortisol levels can induce various adverse effects, screening cortisol and cortisol analogues is important for monitoring stress levels and for identifying drug candidates. A novel cell-based sensing system was adopted for rapid screening of cortisol and its functional analogues under complex cellular regulation. We used glucocorticoid receptor (GR) fused to a split intein which reconstituted with the counterpart to trigger conditional protein splicing (CPS) in the presence of targets. CPS generates functional signal peptides which promptly translocate the fluorescent cargo. The sensor cells exhibited exceptional performance in discriminating between the functional and structural analogues of cortisol with improved sensitivity. Essential oil extracts with stress relief activity were screened using the sensor cells to identify GR effectors. The sensor cells responded to peppermint oil, and L-limonene and L-menthol were identified as potential GR effectors from the major components of peppermint oil. Further analysis indicated L-limonene as a selective GR agonist (SEGRA) which is a potential anti-inflammatory agent as it attenuates proinflammatory responses without causing notable adverse effects of GR agonists.
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