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www.MedChemE
MedChemExpress
PROTACs
(PROteolysis-TArgetingChimeras)
Handbook
www.MedChemE
Inhibitors ? ScreeningLibraries ? Proteins
PROTACs(PROteolysis-TArgetingChimeras)
PROTAC,shortforPROteolysis-TArgetingChimera,isaheterobifunctionalnanomoleculecontainingtwodifferentligands;ligandforubiquitinE3andligandfortargetprotein.Thetwopartsareconnectedbyalinkertoformathree-unitpolymer,targetproteinligand-linker-E3ligaseligand[1].
OncethePROTACmoleculeentersthecell,ligandforproteinofinterest(POI)canspecificallybindtothecorrespondingtargetprotein,whileE3ligaseligandcanrecruitE3ligasetoformthetrimercomplexofPOI-Linker-E3ligase,inwhichE3ligasemediatesubiquitinationonPOIbyubiquitinfromenzymeE2.POIlabeledbyubiquitinisrecognizedanddegradedbytheproteasomesystem.ItisnotnecessaryforPOIligandtooccupythebindingsiteforalongtimeduringthisprogressbecauseofinstantaneousubiquitinationafterthetransientformationoftheternarycomplex,soPROTACcanbereusedmanytimesincells[2].
Ub
NH2
E2
E3
Target
Ligase
Protein
PROTAC
Figure1.CompositionofPROTACs[1].
Ub
NH2
Ub
NH2
E2
E2
E3
Target
PROTAC
E3
Target
Ligase
Protein
Ligase
Protein
Ternary
Complex
Catalytic-PROTACisRecycled
Ub
Ub
Ub
Ub
NH2
Target
Protein
PeptideFragments
Proteasome
Polyubiquitination
Figure2.PROTAC-mediateddegradationoftargetproteinsthroughtheUPS[2].
MCE
MasterofBioactiveMolecules
PROTACimprovesthedrugabilityofprotein
Comparedwithtraditionalsmallmoleculeswhichneedtoknowthebindingsiteandmechanismoftargetprotein,PROTACignoresthemechanismofthetargetproteinitselfanddirectlydegradestargetproteinafterubiquitinlabeling.Inaddition,duetoitsspecificmechanism,itrequiresonlyasmallamounttobeeffective,oftenatthenanomolarlevel.PROTACisdevoidofdrugresistance,andhasbecomeasolutiontotheundruggableproblemofmanytumorin
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