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Cell signalling ,[object Object],[object Object],[object Object]
Previous discussion ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Today ,[object Object],[object Object],[object Object],[object Object],[object Object]
Signal Reception: G Protein-Coupled Receptors
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neurotransmitter receptors ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The G Protein-Coupled Receptor (GPCR) Superfamily ,[object Object],[object Object],[object Object],[object Object],[object Object]
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[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
[object Object],[object Object]
Almost all Receptors Comprise a Number of Subtypes ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Regulation of G protein-coupled receptor function ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
D D D D α α β α γ ,[object Object],[object Object],[object Object],(2)  Phosphorylation P  P (3)  Arrestin binding Arrestin P  P Arrestin P  P Clathrin ,[object Object],[object Object],[object Object],(5)  Endocytosis Endosomes Arrestin P  P  D (7)  Recycling ,[object Object],[object Object],[object Object],[object Object],(8 )  Traffic to lysosomes Lysosomes Mechanisms of Receptor Regulation
Another Receptor – G Protein Cycle
Structure, function and mechanisms of G-Proteins
What are G-proteins? ,[object Object],[object Object],[object Object],Fig.  15.1 Examples of GTPase proteins Ras, Cdc-42 (hormone, GF, drug)
1994  Nobel Prize in Medicine, Alfred Gilman and  Martin Rodbell, for their „discovery of G-Proteins and the role of these proteins in signal  transduction in cells.“
G-Protein = Guanine-nucleotide binding protein (GNBD) Guanine Ribose Phosphates   1 2 5 4 3 α   1 3 4 2 6 5 7 8 9 Guanosine Ester Anhydride Guanosine-triphosphate - GTP
G-Protein families ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
GTPases and disease. ,[object Object],[object Object],[object Object]
G-proteins are tightly regulated ,[object Object],[object Object],[object Object],[object Object]
The heterotrimeric G proteins transmit signals from a variety of cell surface   receptors to enzymes and channels  ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],Structure  of G proteins: The  nucleotide binding site  in G   consists of loops that extend out from the edge of a 6-stranded   -sheet .   Three  switch domains  have been identified, that change position when GTP substitutes for GDP on  G  .
[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],Most GTP-binding proteins depend on  helper proteins :  GAPs ,  G TPase  A ctivating  P roteins, promote GTP hydrolysis.
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],GEFs ,  G uanine  N ucleotide  E xchange Factors, promote GDP/GTP exchange.
   &    subunits have covalently attached  lipid anchors  that bind a G-protein to the plasma membrane cytosolic surface. Adenylate Cyclase  (AC) is a transmembrane protein, with cytosolic domains forming the catalytic site. The    subunit of a G-protein ( G  ) binds  GTP , & can hydrolyze it to GDP + P i .
 
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object]
Fig 15.3  The G Protein Cycle
G Protein-Linked Receptors
G Protein-Linked Receptors
G Protein-Linked Receptors
G Protein-Linked Receptors note how activation is reversible
G Protein-Linked Receptors the more ligand binding, the more K +  in cytoplasm
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object]
How G-protein-coupled receptors work (1) extracellular space cytosol    heterotrimeric  G-protein ‘ 7TM’ - receptor GDP GDP GTP Ligand    N
How G-protein-coupled receptors work (2) inactive    GDP P active N  GTP   N
How G-protein-coupled receptors work (3) ATP inactive inactive active cAMP cAMP Protein kinase A  Phosphorylation of multiple target proteins active Adenylate cyclase    GTP
Some G-proteins are inhibitory  -Adrenoceptor  2 -Adrenoceptor AC active AC inactive  s GTP  i GTP
 -Subunits of G proteins may have regulatory activity, too Muscarinic (M 2 ) acetylcholine receptor K ir AC inactive K +    i GTP
G  -proteins regulate diverse effector systems  q phospholipase C   PIP 2 IP 3  + DAG  protein kinase  C  phosphorylation of multiple proteins  Ca ++ ER  t cGMP phosphodiesterase   cGMP    s adenylate cyclase   protein kinase  A  cAMP    i1 adenylate cyclase   protein kinase  A  cAMP  
Many transmitters have multiple GPCR with different downstream signaling mechanisms Norepinephrine,     1 IP 3  + DAG  epinephrine  2 cAMP   1 ,  2   cAMP  Dopamine  D 2  - D 4 cAMP  D 1 , D 5 cAMP  Acetylcholine         IP 3  + DAG   2 , M 3 cAMP 
[object Object]

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Cell signalling 2

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  • 4. Signal Reception: G Protein-Coupled Receptors
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  • 18. Another Receptor – G Protein Cycle
  • 19. Structure, function and mechanisms of G-Proteins
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  • 21. 1994 Nobel Prize in Medicine, Alfred Gilman and Martin Rodbell, for their „discovery of G-Proteins and the role of these proteins in signal transduction in cells.“
  • 22. G-Protein = Guanine-nucleotide binding protein (GNBD) Guanine Ribose Phosphates 1 2 5 4 3 α   1 3 4 2 6 5 7 8 9 Guanosine Ester Anhydride Guanosine-triphosphate - GTP
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  • 37. &  subunits have covalently attached lipid anchors that bind a G-protein to the plasma membrane cytosolic surface. Adenylate Cyclase (AC) is a transmembrane protein, with cytosolic domains forming the catalytic site. The   subunit of a G-protein ( G  ) binds GTP , & can hydrolyze it to GDP + P i .
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  • 42. Fig 15.3 The G Protein Cycle
  • 46. G Protein-Linked Receptors note how activation is reversible
  • 47. G Protein-Linked Receptors the more ligand binding, the more K + in cytoplasm
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  • 53. How G-protein-coupled receptors work (1) extracellular space cytosol    heterotrimeric G-protein ‘ 7TM’ - receptor GDP GDP GTP Ligand    N
  • 54. How G-protein-coupled receptors work (2) inactive    GDP P active N  GTP   N
  • 55. How G-protein-coupled receptors work (3) ATP inactive inactive active cAMP cAMP Protein kinase A Phosphorylation of multiple target proteins active Adenylate cyclase    GTP
  • 56. Some G-proteins are inhibitory  -Adrenoceptor  2 -Adrenoceptor AC active AC inactive  s GTP  i GTP
  • 57.  -Subunits of G proteins may have regulatory activity, too Muscarinic (M 2 ) acetylcholine receptor K ir AC inactive K +    i GTP
  • 58. G  -proteins regulate diverse effector systems  q phospholipase C  PIP 2 IP 3 + DAG protein kinase C  phosphorylation of multiple proteins Ca ++ ER  t cGMP phosphodiesterase  cGMP   s adenylate cyclase  protein kinase A  cAMP   i1 adenylate cyclase  protein kinase A  cAMP 
  • 59. Many transmitters have multiple GPCR with different downstream signaling mechanisms Norepinephrine,  1 IP 3 + DAG  epinephrine  2 cAMP   1 ,  2 cAMP  Dopamine D 2 - D 4 cAMP  D 1 , D 5 cAMP  Acetylcholine       IP 3 + DAG   2 , M 3 cAMP 
  • 60.

Notas do Editor

  1. D3 is somewhat mysterious – some references say it drops cAMP. Need to find out more about that.