Zusammenfassung der Ressource
GPCRs
- Structure?
- 7 trans-membrane domains
- are trimeric g-proteins: alpha, beta and
gamma subunits.
- The G-alpha subunit is commonly
responsible for most biological effects
- are guanine nucleotide-binding proteins
- Activation?
- Bind guanine-diphosphate (GDP) in inactive state.
Bind guanine-triphosphate (GTP) in their active state.
- can be stimulatory or inhibitory
- 1. G- protein rests in its inactive state, bound to GDP
- 2. When the receptor is activated, the G-protein exchanges GDP for GTP. On binding to
the 1st messenger, there is a conformational change in the 7 transmembrane receptor.
- 3. The activated G-protein splits and the G-alpha and G-beta-gamma subunits are now available to activate effector proteins.
- 4. The G-alpha subunit slowly hydrolyses GTP to GDP, terminating it's own activity and becoming inactive again. So, the GPCR 'times itself'.
- Roles?
- To couple receptors...
- ...effectors which catalyze
formation of second messengers
- ...directly to ion channels
- to 3 main effector pathways:
- 1. Direct-Effector Linked Pathway
- 2. Adenylyl Cyclase Pathway
- 3. Phospholipase-C Pathway
- control whether we feel
pain, or feel happy.
- Effects of Activation may include:
- Metabolic Changes
- Movement
- Cell Death
- Transcription
- Protein Synthesis