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Repurposing an endogenous degradation domain for antibody-mediated disposal of cell-surface proteins.
Schmitt, Janika; Poole, Emma; Groves, Ian; Owen, David J; Graham, Stephen C; Sinclair, John; Kelly, Bernard T.
Afiliación
  • Schmitt J; Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Hills Road, CB2 0SP, Cambridge, UK.
  • Poole E; Faculty of Medicine, Charité Berlin, 10117, Berlin, Germany.
  • Groves I; Faculty of Medicine, University of Heidelberg, 69210, Heidelberg, Germany.
  • Owen DJ; Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Hills Road, CB2 0SP, Cambridge, UK.
  • Graham SC; Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK.
  • Sinclair J; Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Hills Road, CB2 0SP, Cambridge, UK.
  • Kelly BT; Infection Biology, Global Center for Pathogen and Human Health Research, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
EMBO Rep ; 25(3): 951-970, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38287192
ABSTRACT
The exquisite specificity of antibodies can be harnessed to effect targeted degradation of membrane proteins. Here, we demonstrate targeted protein removal utilising a protein degradation domain derived from the endogenous human protein Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9). Recombinant antibodies genetically fused to this domain drive the degradation of membrane proteins that undergo constitutive internalisation and recycling, including the transferrin receptor and the human cytomegalovirus latency-associated protein US28. We term this approach PACTAC (PCSK9-Antibody Clearance-Targeting Chimeras).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Serina Endopeptidasas / Proproteína Convertasa 9 Límite: Humans Idioma: En Revista: EMBO Rep Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Serina Endopeptidasas / Proproteína Convertasa 9 Límite: Humans Idioma: En Revista: EMBO Rep Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido