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6.8:

חלבוני G מצומדי קולטנים

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G-protein Coupled Receptors

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קולטנים מצומדים GPCRs או G לחלבון, הם סוג נוסף של חלבון קרום אינטגרלי. החלק החוץ-תאי שלהם בולט מתוך הקרום ומכיל אתר קישור לליגנד עבור מגוון רחב של תרכובות. החלק התוך-תאי מוצמד לחלבון G המורכב משלוש תתי-יחידות שונות, אלפא, בטא וגמא.כאשר הליגנד נקשר, הקולטן משנה צורה וגורם לגואנוזין דיפוספט, או GDP, הקשור לתת-יחידה אלפא, להשתחרר ולהיות מוחלף על-ידי מולקולת גואנוזין טריפוספט, או מולקולת GTP. ה‫שניים האלו מתנתקים מתתי-יחידות בטא וגמא. כעת, שתי קבוצות החלקיקים חופשיות לנוע בתוך הציטופלזמה ולבוא במגע עם חלבוני אפקטור אחרים המפעילים סדרה של תגובות שרשרת תוך-תאיות של איתות שמכוונות ומגבירות את האות.כדי לסיים את התהליך, ה-GTP עובר הידרוליזה ל-GDP, ותתי-יחידות חלבון ה-G מתארגנות חזרה לצורתן הלא פעילה, ומשאירות את ה-GPCR מוכן לאות חדש.

6.8:

חלבוני G מצומדי קולטנים

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.

The G-protein or guanine nucleotide-binding protein, is a large heterotrimeric complex. Its three subunits are labeled alpha (α), beta (β), and gamma (γ). When the receptor is unbound or resting, the α-subunit binds a guanosine diphosphate molecule or GDP, and all three subunits are attached to the receptor.

When a ligand binds the receptor, the α-subunit releases the GDP and binds a molecule of guanosine triphosphate (GTP). This action releases the α-GTP complex and the β-γ complex from the receptor. The α-GTP can move along the membrane to activate second messenger pathways such as cAMP. However there are different types of α-subunits and some are inhibitory, turning off cAMP.

The β-γ complex may interact with potassium ion channels which release potassium (K+) into the extracellular space resulting in hyperpolarization of the cell membrane. This type of ligand-gated ion channel is called a G-protein coupled inwardly rectifying potassium channel or GIRK.

Ligands do not permanently bind the receptor. When the ligand leaves the receptor, it becomes available for the G-protein units to recouple and reattach. Before this though, nearby enzymes must hydrolyze the GTP attached to the α-subunit back into GDP. Once this is achieved, the β-γ complex reassembles with the GDP-α complex, and the whole G-protein reattaches to its receptor domain.

Common G-protein coupled receptors are: muscarinic acetylcholine receptors found in skeletal muscles, Beta-1 adrenergic receptors in the heart, and vasopressin receptors on smooth muscle cells. In sensory systems, like olfactory receptors and some taste receptors, the binding ligands are environmental molecules. For example, sucrose molecules bind G-protein coupled receptors resulting in the perception of sweet taste.

Alterations in G-protein coupled receptors may play a substantial role in mood disorders, like depression. Serotonin is a ligand for the 5HT1A receptor, a G-protein coupled receptor. It has been suggested that, in depression, interactions between the ligand and the receptor are changed; either the ligand does not bind long enough or the receptor does not fully respond. This results in poor serotonergic signaling which manifests as depression.

Suggested Reading

Gurevich, Vsevolod V., and Eugenia V. Gurevich. “Molecular Mechanisms of GPCR Signaling: A Structural Perspective.” International Journal of Molecular Sciences 18, no. 12 (November 24, 2017). [Source]

Katritch, Vsevolod, Vadim Cherezov, and Raymond C. Stevens. “Structure-Function of the G-Protein-Coupled Receptor Superfamily.” Annual Review of Pharmacology and Toxicology 53 (January 6, 2013): 531–56. [Source]

Bar-Shavit, Rachel, Myriam Maoz, Arun Kancharla, Jeetendra Kumar Nag, Daniel Agranovich, Sorina Grisaru-Granovsky, and Beatrice Uziely. “G Protein-Coupled Receptors in Cancer.” International Journal of Molecular Sciences 17, no. 8 (August 12, 2016). [Source]