Detailed Information on Publication Record
2022
Non-psychotropic cannabinoids as inhibitors of TET1 protein
ANTONYOVÁ, Veronika, Zdeněk KEJÍK, Tereza BROGYANYI, Robert KAPLÁNEK, Kateřina VESELÁ et. al.Basic information
Original name
Non-psychotropic cannabinoids as inhibitors of TET1 protein
Authors
ANTONYOVÁ, Veronika (203 Czech Republic), Zdeněk KEJÍK (203 Czech Republic), Tereza BROGYANYI (203 Czech Republic), Robert KAPLÁNEK (203 Czech Republic), Kateřina VESELÁ (203 Czech Republic), Nikita ABRAMENKO (203 Czech Republic), Tomáš OCELKA (203 Czech Republic), Michal MASAŘÍK (203 Czech Republic, belonging to the institution), Adam MATKOWSKI (616 Poland), Jakub GBUREK (616 Poland), Renata ABEL (616 Poland), Andrean GOEDE (276 Germany), Robert PREISSNER (276 Germany), Petr NOVOTNÝ (203 Czech Republic) and Milan JAKUBEK (203 Czech Republic, guarantor)
Edition
Bioorganic Chemistry, San Dieo, ACADEMIC PRESS INC ELSEVIER SCIENCE, 2022, 0045-2068
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30105 Physiology
Country of publisher
Slovenia
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.100
RIV identification code
RIV/00216224:14110/22:00125768
Organization unit
Faculty of Medicine
UT WoS
000819757600001
Keywords in English
Cannabinoids; TET1 protein; Iron chelation; DNA methylation; Epigenetic
Tags
International impact, Reviewed
Změněno: 19/7/2022 10:51, Mgr. Tereza Miškechová
Abstract
V originále
Non-psychotropic cannabinoids (e.g., cannabidiol, cannabinol and cannabigerol) are contained in numerous alimentary and medicinal products. Therefore, predicting and studying their possible side effects, such as changes in DNA methylation, is an important task for assessing the safety of these products. Interference with TET enzymes by chelating ferrous ions can contribute to the altered methylation pattern. All tested cannabinoids displayed a strong affinity for Fe(II) ions. Cannabidiol and cannabinol exhibited potent inhibitory activities (IC50 = 4.8 and 6.27 μM, respectively) towards the TET1 protein, whereas cannabigerol had no effect on the enzyme activity. An in silico molecular docking study revealed marked binding potential within the catalytic cavity for CBD/CBN, but some affinity was also found for CBG, thus the total lack of activity remains unexplained. These results imply that cannabinoids could affect the activity of the TET1 protein not only due to their affinity for Fe(II) but also due to other types of interactions (e.g., hydrophobic interactions and hydrogen bonding).
Links
LM2018133, research and development project |
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NU21-08-00407, research and development project |
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TN01000013, research and development project |
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