| Literature DB >> 36197299 |
Berend Gagestein1, Johannes H von Hegedus2, Joanneke C Kwekkeboom2, Marieke Heijink3, Niek Blomberg3, Tom van der Wel1, Bogdan I Florea4, Hans van den Elst4, Kim Wals1, Herman S Overkleeft4, Martin Giera3, René E M Toes2, Andreea Ioan-Facsinay2, Mario van der Stelt1.
Abstract
The fish oil constituent docosahexaenoic acid (DHA, 22:6 n-3) is a signaling lipid with anti-inflammatory properties. The molecular mechanisms underlying the biological effect of DHA are poorly understood. Here, we report the design, synthesis, and application of a complementary pair of bio-orthogonal, photoreactive probes based on the polyunsaturated scaffold DHA and its oxidative metabolite 17-hydroxydocosahexaenoic acid (17-HDHA). In these probes, an alkyne serves as a handle to introduce a fluorescent reporter group or a biotin-affinity tag via copper(I)-catalyzed azide-alkyne cycloaddition. This pair of chemical probes was used to map specific targets of the omega-3 signaling lipids in primary human macrophages. Prostaglandin reductase 1 (PTGR1) was identified as an interaction partner that metabolizes 17-oxo-DHA, an oxidative metabolite of 17-HDHA. 17-oxo-DHA reduced the formation of pro-inflammatory lipids 5-HETE and LTB4 in human macrophages and neutrophils. Our results demonstrate the potential of comparative photoaffinity protein profiling for the discovery of metabolic enzymes of bioactive lipids and highlight the power of chemical proteomics to uncover new biological insights.Entities:
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Year: 2022 PMID: 36197299 PMCID: PMC9585591 DOI: 10.1021/jacs.2c06827
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 16.383