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Updated: May 29, 2026

Reverse Yeast Two-hybrid System to Identify Mammalian Nuclear Receptor Residues that Interact with Ligands and/or Antagonists
Published on: November 15, 2013
[Nuclear receptors PPAR as a drug target in metabolic disorders]
Marta Stolarczyk1, Wojciech Gutman, Rafał A Derlacz
1Zakład Regulacji Metabolizmu, Instytut Biochemii, Wydział Biologii UW, Warszawa.
Abstract:
Nuclear receptors regulate many basic cellular processes and their malfunction can lead to serious consequences including metabolic disorders, obesity and type 2 diabetes. Among many nuclear receptor families, the best known for their therapeutic use are the PPARs. These are key transcription factors determining, proper cellular metabolism of glucose and lipids, tissue sensitivity to insulin, appropriate immune responses including inflammatory processes and finally cell division and differentiation. Currently two types of PPAR activators are in medical use: in the therapy of type 2 diabetes--thiazolidinediones (TZDs), which act via PPARgamma receptors and in the treatment of dyslipidemia-fibrates, which act via PPARalpha receptors. The search for new drugs acting through PPAR mechanism consists in the design of new molecules with tissue specific proprieties, which would selectively bind and modulate the activity of appropriate receptors, thus reducing the number of adverse events typically observed with the use of full agonists. These molecules have been named selective nuclear receptor modulators (SNuRMs).
Insights
Nuclear receptors, particularly PPARs, are crucial for cellular metabolism and insulin sensitivity. Developing selective nuclear receptor modulators (SNuRMs) aims to reduce adverse effects from current PPAR therapies.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Pharmacology
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