A click chemistry approach identifies target proteins of xanthohumol

Brodziak-Jarosz, Lidia and Fujikawa, Yuuta and Pastor-Flores, Daniel and Kasikci, Sonay and Jirasek, Petr and Pitzl, Sebastian and Owen, Robert W. and Klika, Karel D. and Gerhaeuser, Clarissa and Amslinger, Sabine and Dick, Tobias P. (2016) A click chemistry approach identifies target proteins of xanthohumol. MOLECULAR NUTRITION & FOOD RESEARCH, 60 (4). pp. 737-748. ISSN 1613-4125, 1613-4133

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Abstract

ScopeMany phytochemicals with beneficial pharmacological properties contain electrophilic sites, e.g. ,-unsaturated carbonyl (enone) groups. There is increasing evidence that many biological effects of electrophilic compounds depend on covalent conjugation to reactive protein thiols. For example, the reaction of electrophiles with cysteinyl residues of the sensor protein Keap1 activates the cell-protective Nrf2 response. Thus it is of interest to identify more generally the proteins to which small molecule electrophiles bind covalently. Methods and resultsHere we use a Click chemistry approach to identify target proteins of the chemopreventive phytochemical xanthohumol (XN), an enone-containing chalcone from hops (Humulus lupulus L.). Using an alkynylated analog of XN (XN-alkyne), we purified covalent protein-electrophile conjugates from cell lysates. We confirm the previously described conjugation of XN to Keap1. One of the newly identified candidate target proteins is glucose-6-phosphate dehydrogenase (G6PDH). We confirm that XN attenuates intracellular G6PDH activity at low micromolar concentrations. ConclusionWe find support for the notion that XN modulates multiple pathways and processes by covalent modification of proteins with reactive cysteines.

Item Type: Article
Uncontrolled Keywords: PRENYLATED CHALCONES; QUINONE REDUCTASE; CANCER-CELLS; AGENTS; HOPS; APOPTOSIS; BEER; ACTIVATION; HEALTH; SITES; Click chemistry; Electrophilic compounds; Keap1-Nrf2 pathway; Protein thiols; Xanthohumol
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie
Chemistry and Pharmacy > Institut für Organische Chemie > Arbeitskreis Dr. Sabine Amslinger
Depositing User: Dr. Gernot Deinzer
Date Deposited: 22 Mar 2019 06:53
Last Modified: 22 Mar 2019 06:53
URI: https://pred.uni-regensburg.de/id/eprint/3147

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