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Lecture 11: GPCR pathways. Fain Chapter 4 10/7/09. Kao - high transmission fiber optic cables from pure materials. Fiber optic networks. Current amount of fiber goes around world 25,000 times. Boyle and Smith - CCD. Central dogma DNA mRNAprotein. The amazing ribosome creates proteins.
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Lecture 11: GPCR pathways Fain Chapter 4 10/7/09
Kao - high transmission fiber optic cables from pure materials
Fiber optic networks Current amount of fiber goes around world 25,000 times
Ada Yonath crystallizes ribosome Small subunit - 32 proteins Large subunit - 46 proteins Geobacillus stearothermophilus - hot springs Haloarcula marismortui - Dead Sea
Homework #5 • Gene duplication • Build a tree (Pasteur) • Think about gene function (OMIM) • Locate genes (Map viewer)
GNAI2 Homework #1: GNA trees GNAI3 GNAI1 GNAT3 Taste Cone Rod GNAT2 GNAT1
Link to chromosome location Click here
Can remove those you don’t want (rna maps) Highlight items and then click remove Then update with OK
Location of GNAT and GNAI GNAT1 GNAI2 3p21 GNAT2 GNAI3 1p13 GNAT3 GNAI1 7q21
Rest of semester • Individual senses • Fain chapters • Primary literature • Midterm project • Trp channel analysis - next week • Individual project topics • Diversity of one sense across organisms • Signal transduction • Sensory diversity within one organism
The wonders of G protein signaling • Signal amplification • Control, regulation and specificity • Evolution of diversity • Gene expression
Ch4: Metabotropic signal transduction • Indirect link from receptor to channel • Use messenger system • Receptor G protein Effector 2nd messenger Channel Neural signal • Receptors are G protein coupled • Similar to hormone and neurotransmitter signal transduction mechanisms
Metabotropic sensory transduction Channel Figure 4.1
G proteins activate effectors • Adenylyl cyclase = makes cAMP • Guanyl cyclase = makes cGMP • Phospholipase C = makes DAG and IP3 • Phospholipase A = makes arachidonic acid • Phosphodiesterase = hydrolyzes cAMP or cGMP • 2nd messengers open/close channels • change ion concentration and membrane potential
Diversity of GPCRs • Human genome • 1500-2000 GPCRs (3-5% of genome) • Kinds • Hormone receptors • FSH, Oxytocin, Vasopressin • Synaptic transmitters • Dopamine, opiates, glutamate • Sensory receptors • Olfactory receptors • Visual pigments • Taste receptors for bitter, sweet and AA
Basic GPCR structure • 7 TM regions • Phosphorylation sites on C terminus • G protein binds to C terminus and intracellular loops 2 and 3 Figure 4.3
Basic GPCR structure • 7 TM regions • Phosphorylation sites on C terminus • G protein binds to C terminus and intracellular loops 2 and 3 • Ligand binds either • in membrane • norepinephrine • olfaction • extracellular site • glutamate • GABA Figure 4.3
Xray crystal structure of GPCR Rhodopsin 11-cis retinal Palczewski et al 2000
GPCR phylogeny N=neurotransmitter P=peptides S=sensory Yokoyama and Starmer 1996
G proteins • Ones that interact with GPCR are trimeric - and • Act like switch • Binding site on for GDP • If exchange GDP for GTP, becomes activated • Dissociates from
G protein= • Numbers of different versions of subunits in human genome • 20-30 G • 5 G • 12 G
G GPA Ancient G proteins
G • Gs stimulates adenylate cyclase • includes olfactory
G • Gs stimulates adenylate cyclase • includes olfactory • Gi/Go • Inhibitory and other • Includes vision and taste Transducin gustducin
G • Gs stimulates adenylate cyclase • includes olfactory • Gi/Go inhibits • Includes vision and taste • Gq • Activates PLC
G and tethered to membrane tethered by geranyl geranyl (gg) tethered by palmitoyl (p)
Activated GPCR activates G protein GPCR GDP
+ GTP Get dissociation of G and G GTP binding activates G GPCR* GDP GTP
GTP binding activates G Effector + AMP cAMP Both G and G can activate effector molecules
GDP GTP hydrolysis inactivates GRecombines with G + + GDP Hydrolysis to GDP G will hydrolyze its own GTP slowly GTPase activating proteins speed hydrolysis Regulator of G protein signaling (RGS)
Lichtarge wanted to explain properties of G proteins • How are they kept inactive? • G-G binding • How do they interact with receptors? • GPCR binding • How are they activated? • GDP-GTP binding pocket • How do they interact with effectors? • How are they inactivated?