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Related Concept Videos

Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

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G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical,...
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GPCRs are primarily responsible for our sense of smell, taste, and vision.  The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
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Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
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G Protein-coupled Receptors01:15

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G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
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G-protein Coupled Receptors01:21

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G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
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Related Experiment Video

Updated: Mar 26, 2026

A Pipeline to Investigate the Structures and Signaling Pathways of Sphingosine 1-Phosphate Receptors
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Insight into SUCNR1 (GPR91) structure and function.

Julie Gilissen1, François Jouret2, Bernard Pirotte3

  • 1Laboratory of Molecular Pharmacology, GIGA-Molecular Biology of Diseases, University of Liège, Liège, Belgium; Laboratory of Medicinal Chemistry, Centre for Interdisciplinary Research on Medicines (CIRM), University of Liège, Belgium.

Pharmacology & Therapeutics
|January 26, 2016
PubMed
Summary

Succinate receptor 1 (SUCNR1) is a G protein-coupled receptor activated by succinate. This review explores SUCNR1

Keywords:
DiabetesGPR91HypertensionIschemia–reperfusion injurySUCNR1Succinate

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Pharmacology

Background:

  • G protein-coupled receptors (GPCRs) are a major drug target class.
  • SUCNR1, initially an orphan receptor, is activated by succinate, a metabolic intermediate.
  • Succinate signaling via SUCNR1 is implicated in cellular stress and metabolism.

Purpose of the Study:

  • To review the structural features, ligands, and signaling pathways of SUCNR1.
  • To discuss the pathophysiological roles of SUCNR1 in various diseases.
  • To highlight SUCNR1 as a potential drug target for novel therapeutics.

Main Methods:

  • Literature review of structural and functional studies on SUCNR1.
  • Analysis of in vitro and in vivo data on SUCNR1 signaling.
  • Discussion of the link between SUCNR1 pathways and disease.

Main Results:

  • SUCNR1 is activated by succinate, influencing cellular metabolism and stress responses.
  • SUCNR1 is involved in hypertension, inflammation, and angiogenesis.
  • Its precise signaling mechanisms and physiological roles require further investigation.

Conclusions:

  • SUCNR1 is a crucial regulator of physiological processes with significant therapeutic potential.
  • Further research into SUCNR1 modulators is essential for drug development.
  • Understanding SUCNR1 pathways is key to addressing related diseases.