Tyrosine kinases

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Michael Jeltsch Tyrosine Tyrosine kinases kinases ttp://msbl.helsinki.fi/tksemina

description

Tyrosine kinases. http://msbl.helsinki.fi/tkseminar. Biological responses. Activation of Gene expression. Signal trans- duction. Signaling molecules. Producer cell. RNA. Receptor binding. Target cell. proliferation, differentiation, migration, metabolism, etc. - PowerPoint PPT Presentation

Transcript of Tyrosine kinases

Page 1: Tyrosine kinases

Michael Jeltsch

Tyrosine Tyrosine kinaseskinaseshttp://msbl.helsinki.fi/tkseminar

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Producercell Target

cell

Receptor binding

Signaling molecules

Signal trans-duction

Activation ofGene expression

proliferation, differentiation, migration, metabolism, etc.proliferation, differentiation, migration, metabolism, etc.

RNA

Biological Biological responsesresponses

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Cell surface Cell surface receptorsreceptors

ion-channel-linked

guanylylcyclases

tyrosinekinases

tyrosine kinaseassociated

tyrosinephosphatases

serin/threoninekinases

enzyme-linked G-protein-linked

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extracellular

juxtamembranetransmembrane

tyrosine kinase

carboxy-terminal tail

a

ligand bindingNH2

COOH

ATP

substratebinding

Receptor Tyrosine Receptor Tyrosine KinasesKinases

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Michael Jeltsch

VEGF xVEGF xVEGF-R1VEGF-R1

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ssss

ss

ss

EGF-R IGF-1-R FGF-RPDGF-R VEGF-R3

RTK RTK subclassessubclasses

I II III IV

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Modular structure of EC Modular structure of EC domainsdomains

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RTK RTK ligandsligands

• Some RTKs need two ligands for activation

• Extracellular matrix components (HSPGs)

• Membrane-bound proteins (ephrins)

• Cytokines (EGF, FGF, CSF-1, insulin)

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a

a

aa

PPPPPP

Signaling through an RTKSignaling through an RTK

aa

PPPPPP

a

a

a

a

a

a

a

a

a

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Dimerization or oligomerizationDimerization or oligomerization

• Bivalent ligand(e.g. VEGF, PDGF)

• Ligand-induced conformational change(probably EGF)

• Intracomplex conformational change(e.g. insulin)

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Transmembrane signal Transmembrane signal transfertransfer

• Exact mechanism unknown• Same or similar mechanism for all

RTKs (evidence from hybrid receptors)

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AutophosphorylationAutophosphorylation

• Purposes:- Regulation of tyrosine kinase activity- Recruitment of signaling molecules

• Specific Tyr residues, usually outside thetyrosine kinase domain (juxtamembranedomain, cytoplasmic tail, kinase insert)

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• SH2 (Src-homolgy 2)

• WW

• SH3 (Src-homolgy 3)• PH (pleckstrin homology)/FYVE

• PTB (phosphotyrosine binding)

Signaling proteins are modular moleculesSignaling proteins are modular molecules

SH2 PTB SH3 PH/FYVE PZB WW

• PDZ

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SH2 (Src-homology 2)/SH2 (Src-homology 2)/PTB (phosphotyrosine binding)PTB (phosphotyrosine binding)

• Bind to PY (and sometimes Y)• Specificity is achieved through the context• SH2: 1-6 amino acids C-terminal to PY• PTB: 3-5 amino aids N-terminal to PY (or Y)

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SH3 (Src-homology 3)SH3 (Src-homology 3)

• Binds to proline motif PXXP

WWWW

• Binds to proline motif PXPX

SH3 & SH3 & WWWW

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PH (pleckstrin homology)/FYVEPH (pleckstrin homology)/FYVE• PH domain binds to phosphoinositides (membrane-

localization)• FYVE domain binds specifically PtdIns-3-P

PDZ (PSD-95, DDLP, ZP1)PDZ (PSD-95, DDLP, ZP1)• Bind to hydrophobic C-terminal strtches of target proteins

PH/FYVE/PDZPH/FYVE/PDZ

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SH2PTB

P

P

PH/FYVE SH3 WW PDZ Enzymaticactivity

KinasesPhosphatasesPLC-Ras-GAPRho-GRF

Cellular Targets

membrane

Assembly of a specific signaling Assembly of a specific signaling complexcomplex

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Myristyl. PTB

PH

TM P P P P P

P P P P P P

P P P

Membranelocalization

Receptorbinding Tyrosines

PP

P

FRS2

Dos

LAT

Indirect recruitment is the main recruitment methodfor some receptors (insulin receptor, FGF receptors)

Docking Docking proteinsproteins

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Topics in activation of effector Topics in activation of effector proteinsproteins

1. Activation by Membrane Translocation

2. Activation by a Conformational Change

3. Activation by Tyrosine Phosphorylation

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1. Membrane translocation

2.ConformationalChange 3. Tyrosine Phosphorylation

Activation of signaling molecules: PDGF Activation of signaling molecules: PDGF receptorreceptor

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Intracellular Signaling Intracellular Signaling PathwaysPathways

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Signal Signal TerminationTermination

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• Ligand-induced oligomerization orconformational change

• Autophosphorylation/crossphosphorylation• Recruitment of signaling

molecules tophosphorylated tyrosines (“signalingcomplexes”)• Termination of Signaling (endocytosis)

3 Steps to 3 Steps to activationactivation

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Intracellular vs. Transmembrane Receptor Tyrosine Intracellular vs. Transmembrane Receptor Tyrosine Kinases:Kinases:

Phylogenetic tree of tyrosine kinasesPhylogenetic tree of tyrosine kinases

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Cytoplasmic Tyrosine Cytoplasmic Tyrosine KinasesKinases

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Tyrosine kinase-derived Tyrosine kinase-derived oncogenesoncogenes

oncogene retrovirus cellular counterpart

v-src Rous sarcoma c-srcv-erbB avian erythroblastosis EGF receptorv-fms McDonough feline

sarcomaCSF-1 receptor

v-kit feline sarcoma SCF receptorv-abl Abelson murine

leukemiac-abl

v-sis simian sarcoma PDGF

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ss

VEGF-R3

Dominant Negative Dominant Negative Receptors:Receptors:

VEGFR-3 mutations in hereditary lymphedema

S641P

P1114L

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Further Further readingreading

Schlessinger, J. (2000): Cell Signaling by Receptor Tyrosine Kinases.Cell, Vol. 103, 211-225.