AI Article Synopsis

  • Nrf2 is a key protein that helps regulate the body's antioxidant defenses and is usually kept in check by another protein, Keap1.
  • Researchers developed a quantum model to identify small molecules that can disrupt the Nrf2-Keap1 interaction and promote the activation of Nrf2 for better antioxidant responses.
  • By screening over 18 million chemicals virtually and testing the top candidates in the lab, they found several potential new compounds that activate Nrf2 and may offer protection against oxidative stress and toxins, streamlining the drug development process.

Article Abstract

Nuclear factor erythroid 2-related factor 2 (Nrf2) is the master transcription factor of the antioxidant response element pathway, coordinating the induction of detoxifying and antioxidant enzymes. Nrf2 is normally sequestered in the cytoplasm by Kelch-like ECH-associating protein 1 (Keap1). To identify novel small molecules that will disturb Nrf2-Keap1 binding and promote activation of the Nrf2- antioxidant response element pathway, we generated a quantum model based on the structures of known Nrf2- antioxidant response element activators. We used the quantum model to perform in silico screening on over 18 million commercially available chemicals to identify the structures predicted to activate the Nrf2- antioxidant response element pathway based on the quantum model. The top hits were tested in vitro, and half of the predicted hits activated the Nrf2-antioxidant response element pathway significantly in primary cell culture. In addition, we identified a new family of Nrf2-antioxidant response element-activating structures that all have comparable activity to tBHQ and protect against oxidative stress and dopaminergic toxins in vitro. The improved ability to identify potent activators of Nrf2 through the combination of in silico and in vitro screening described here improves the speed and cost associated with screening Nrf2-antioxidant response element -activating compounds for drug development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484224PMC
http://dx.doi.org/10.1111/cbdd.12040DOI Listing

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