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Enhanced Transduction of P2X7-Expressing Cells with Recombinant rAAV Vectors.
Mann, Anna Marei; Schäfer, Waldemar; Adriouch, Sahil; Börner, Kathleen; Grimm, Dirk; Braren, Ingke; Koch-Nolte, Friedrich.
Afiliação
  • Mann AM; Institute of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Schäfer W; Institute of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Adriouch S; UNIROUEN, INSERM, U1234, Pathophysiology, Autoimmunity, Neuromuscular Diseases and Regenerative THERapies (PANTHER), Normandie University, Rouen, France.
  • Börner K; Department of Infectious Diseases/Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
  • Grimm D; BioQuant, Heidelberg University and German Center for Infection Research (DZIF), Heidelberg, Germany.
  • Braren I; Department of Infectious Diseases/Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
  • Koch-Nolte F; BioQuant, Heidelberg University and German Center for Infection Research (DZIF), Heidelberg, Germany.
Methods Mol Biol ; 2510: 129-144, 2022.
Article em En | MEDLINE | ID: mdl-35776323
ABSTRACT
Adeno-associated viruses (AAV) are useful vectors for transducing cells in vitro and in vivo. Targeting of specific cell subsets with AAV is limited by the broad tropism of AAV serotypes. Nanobodies are single immunoglobulin variable domains from heavy chain antibodies that naturally occur in camelids. Their small size and high solubility allow easy reformatting into fusion proteins. In this chapter we provide protocols for inserting a P2X7-specific nanobody into a surface loop of the VP1 capsid protein of AAV2. Such nanobody-displaying recombinant AAV allow 50- to 500-fold stronger transduction of P2X7-expressing cells than the parental AAV. We provide protocols for monitoring the transduction of P2X7-expressing cells by nanobody-displaying rAAV by flow cytometry and fluorescence microscopy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dependovirus / Vetores Genéticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dependovirus / Vetores Genéticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article