1. Signalling at Cell Surface 2 April 2007

2. Receptors

3. Classification of receptors Intracellular receptors (for lipid soluble messengers) function in the nucleus as transcription factors to alter the rate of transcription of particular genes. Plasma membrane receptors (for lipid insoluble messengers) Receptors function as ion channels receptors function as enzymes or are closely associated with cytoplasmic enzymes receptors that activate G proteins which in turn act upon effector proteins, either ion channels or enzymes, in the plasma membrane.

4. Cell Surface Receptors May work both fast and slow Always use “second messengers”

6. Cell-Surface Receptors Belong to Four Major Classes G protein coupled receptors : epinephrine, serotonin, and glucagon. Ion-channel receptors: acetylcholine receptor at the nerve-muscle junction. Tyrosine kinase linked receptors: cytokines, interferons, and human growth factor. Receptors with intrinsic enzymatic activity

7. Four classes of ligand-triggered cell- surface receptors

8. RECEPTOR ION CHANNELS multi-subunit, transmembrane protein complexes complex is both the receptor and ion channel stimuli: chemical, stretch or voltage stimulus induces conformational change to open or close ion channel two types: 1) ligand-gated ion channel 2) voltage-gated ion channel

9. LIGAND-GATED ION CHANNELS chemical stimuli bind to receptor and open or close ion channel stimuli can be extracellular or intracellular EXTRACELLULAR STIMULI: (neurotransmitters) –e.g. acetylcholine, dopamine, GABA, glutamate INTRACELLULAR STIMULI: (second messengers) –e.g. IP 3, cAMP, cGMP, Ca 2+

10. LIGAND-GATED ION CHANNEL AT THE SYNAPSE occurs at gap (synaspe) between nerve and target cell acetylcholine (ACh) released into synapse ACh binds to ion channel on target cell, opens channel, influx of Na + enzyme acetylcholinesterase released into synapse to breakdown ACh

11. ACETYLCHOLINE ANTAGONISTS very potent neurotoxins bind to receptor and prevent opening of Na + channel –e.g. cobratoxin from Indian cobra – atropine from deadly nightshade – S. American arrow poison (curare) - very fast acting so shot animals don’t run too far

12. VOLTAGE GATED ION CHANNELS ion channel undergoes conformational change folllowing electrical stimulus this “depolarization” opens the channel –leads to flow of Na + into cell –constitutes an “action potential” channel recloses

13. Signaling pathways downstream from G protein coupled receptors (GPCRs) and receptor tyrosine kinases (RTKs)

14. Structural formulas of four common intracellular second messengers.

16. Intracellular proteins Two groups of evolutionary conserved proteins function in signal transduction 1. GTPase switch proteins –Conversion from GDP bound inactive state to GTP-bound active state is mediated by guanine nucleotide exchange factors (GEFs) –Intrinsic GTPase activity hydrolyzes bound GTP to GDP + Pi

17. GTP hydrolysis is accelerated by GTPase accelerating protein (GAPs) Two classes of GTPase switch proteins: –Trimeric (large) G proteins Directly bind to receptors –Monomeric (small) G proteins Linked to receptors via adapter proteins and GEFs

18. Common intracellular signaling proteins

20. 2. Protein kinases and phosphatases –Human genome encodes 500 PKs and 100 PPs –Two types of PK Those that P* OH group on Tyr residue Those that P* OH group on Ser or Thr residues –PK is activated By other kinases By direct binding to other proteins By second messengers

21. Regulation of signaling External signal decreases –Degradation of second mesenger Desensitization to prolonged signaling –Receptor endocytosis Modulation of receptor activity –Phosphorylation –Binding to other proteins

22. G Protein-Coupled Receptors A very large family of receptors coupled to trimeric G proteins Activate or inhibit adenylyl cyclase All have seven membrane spanning region Ligands include: –Hormones, neurotransmitters, light activated receptors (rhodopsins), thousands of odorant receptors

23. GPCRs and G proteins are involved in the regulation of many important physiological functions

25. Signal transducing G protein has 3 subunits –G , Gß and G  G  is the GTPase switch protein and modulates the activity of an effector protein Effector proteins are either membrane bound ion channels or enzymes generating second messengers

33. GPCR-mediated dissociation of trimeric G proteins has been demonstarted in fluorescence energy transfer experiments

37.    GDP   GTP +   GDP  Inactive effector Active effector Pi GTPGDP Agonist-receptor complex     Active effector The activation/deactivation cycle of G proteins

38. G proteins can be linked to: adenylate cyclase –produces cyclic AMP (cAMP) guanyl cyclase –produces cyclic GMP (cGMP) phospholipase C –produces inositol trisphosphate (IP 3 ) and diacyl glycerol (DAG) ion channels

39. G-Protein- Activated Enzymes

40. first messenger receptor transducer amplifier second messenger

41. Activity of  subunits Activation of K + Channels

42. G-Protein-Activated Enzymes Generate new molecules - “second messengers

43. G proteins and cAMP

44. cAMP vs PKA

45. cAMP and gene transcription

46. Epinephrine case Mediates body’s response to stress, when all tissues need glucose and fatty acids to produce ATP ß-adrenergic receptors –Heart muscle: contraction –Smooth muscle cells of intestine: relax  2-adrenergic receptors –Smooth muscle cells of endothelium, skin, kidney and intestine: constrict

47. ß1 and ß2 adrenergic receptors are coupled to stimulatory G protein (Gs) –Actvates adenylyl cyclase  1 adrenergic receptor is coupled to inhibitory G protein (Gi) –Inhibits adenylyl cyclase  2 adrenergic receptor is coupled to Gq that activates another effector enzyme

48. Bacterial toxins –Vibrio cholera Catalyzes chemical modification of Gs  that prevents hydrolysis of GTP to GDP –Active state –Bordetella pertussis Catalyzes chemical modification of Gi  that prevents release of GDP –Inactive state

49. Critical domain of GPCR resides in C3 loop according to chimeric receptor expression experiments

55. Differential modulation of adenylyl cyclase Different hormone-receptor complexes modulate the activity of the same effector molecule –In liver glucagon and epinephrine bind to different receptors but activate the same Gs: same metabolic responses