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Clathrine en Kinase afhankelijke EGFR internalizatie Time (min) EGF Internalized/Surface
 
Dimerization induced by FKBP
Dimerization EGFR induces  Kinase independent EGFR internalization
Res 1005-1017 essential for kinase independent internalization Wang et al 2007
Di-Leucine motif essential for kinase independent internalization Wang et al 2007
Verschillende internalisatie  mechanismes Dimerizatie afhankelijk   Afhankelijk van ubiquitinering
Afbraak van de EGFR in lysosomen
Late endosomen/multi-vesicular bodies
3D morphologie van het MVB
Morphologie van het MVB
Het lysosoom,  het vuilnisvat van de cel lysosoom Late endosomen
[object Object],[object Object],[object Object],[object Object],[object Object]
EGFR ubiquitinering  noodzakelijk voor afbraak
Hoe wordt de EGFR afgebroken?
Valorisatie Doel : Sturen van SMI’s (small molecule inhibitor) Naar intracellulaire locatie van de tumor cel. Langzaam vrijkomen van de remmer.
Antibody fragments: Fab’s  and Nanobodies (VHH) VH CH1 VL CL CH2 CH3 VHH CH2 CH3 Conventional antibody ‘ Heavy chain only’ antibody Fab NB
Nanobody ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Anti-EGFR NB: EGa1 QVQLQESGGGSVQAGGSLKLSCTASGRRFS  TYAVG  WFRQAPGQDREFVA  TISWTNSTDYADSVKG   RFTISRDNAKNTGYLQMNGLKPEDTSVYVCAA  DKWSSSRRSVDYDY   WGQGTQVTVSS QVQLQESGGGLVQAGGSLRLSCAASGRTFS  GFAMG  WFRQAPGKEREFVA  AISWSGGSLLYVDSVKG   RFTISRDNAKNTVHLQMNSLKPEDTAVYYCAA  MVGPPPRSLDYGLGNHYEYDY  WGQGTQVTVSS EVQLVESGGGSVQTGGSLRLTCAASGRTSR  SYGMG  WFRQAPGKEREFVS  GISWRGDSTGYADSVKG   RFTISRDNAKNTVDLQMNSLKPEDTAIYYCAA  AAGSAWYGTLYEYDY   WGQGTQVTVSS QVQLQESGGGLVQPGGSLRLSCAASGRTFS  SYAMG  WFRQAPGKEREFVA  AIRWSGGYTYYTDSVKG   RFTISRDNAKTTVYLQMNSLKPEDTAVYYCAA  TYLSSDYSRYALPQRPLDYDY  WGQGTQVTVSS QVQLQESGGGLVQAGGSLLLSCAASGRTFS  SYAMG  WFRQAPGKEREFVA  AINWSGGSTSYADSVKG   RFTISRDNTKNTVYLQMNSLKPEDTAAFYCAA  TYNPYSRDHYFPRMTTEYDY   WGQGTQVTVSS QVQLQESGGGLVQAGGSLRLSCAASGRTFT  SYAMG  WFRQVPGKEREFVA  ALSTRSAGNTYYADSVKG  RFTISRDNAKNTVYLQMSSLKAEDTAVYYCAA  GYMSSDADPSLAASLHPYDY   WGQGTQVTVSS CDR1 CDR2 CDR2 FR1 FR2 FR3 FR4
Multiple formats of nanobodies Multivalent Improve avidity Crosslinking Multi-specific Increase efficacy Effector domain Improve functionality Extend half-life Therapy
EGFR internalization Via EGFR Oligomerizatie
Epitope specificity  anti-EGFR NBs 7D12 Dom III  9G8 Dom II/III  EgB4 Dom IV  EgC9 Dom I  7D12 Plasma membrane Tyrosine kinase Rob Roovers IV III II I 9G8 EgB4 EgC9
Affinities 7D12-9G8  7D12  9G8 nM 50.0 25.0 12.5 6.25 … Sabrina Oliveira 3T3 2.2 14C cells Nanobody ~ Kd nM ~ IR:protein 7D12 1.5 0.4 9G8 5 0.7 7D12-9G8 1 0.6 7D12-9G8-Alb 2 0.8 EGb4 7 0.4 Cetuximab 0.5 1.4
Some compete with EGF others do not Raimond Heukers
No agonists Raimond Heukers
EGFR internalization Induced by Oligomerization
Nanobody-induced EGFR transport Jeroen Vermeulen
TRI induces EGFR degradation Jeroen Vermeulen
NB-stimulated EGFR degradation depends upon lysosomes Degradation  Degradation in presence of chloroquine Jeroen Vermeulen
 

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