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Identification of Novel Macropinocytosing Human Antibodies by Phage Display and High-Content Analysis.
Ha, K D; Bidlingmaier, S M; Su, Y; Lee, N-K; Liu, B.
Afiliação
  • Ha KD; UCSF Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, CA, United States.
  • Bidlingmaier SM; UCSF Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, CA, United States.
  • Su Y; UCSF Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, CA, United States.
  • Lee NK; UCSF Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, CA, United States.
  • Liu B; UCSF Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, San Francisco, CA, United States. Electronic address: bin.liu@ucsf.edu.
Methods Enzymol ; 585: 91-110, 2017.
Article em En | MEDLINE | ID: mdl-28109445
ABSTRACT
Internalizing antibodies have great potential for the development of targeted therapeutics. Antibodies that internalize via the macropinocytosis pathway are particularly promising since macropinocytosis is capable of mediating rapid, bulk uptake and is selectively upregulated in many cancers. We hereby describe a method for identifying antibodies that internalize via macropinocytosis by screening phage-displayed single-chain antibody selection outputs with an automated fluorescent microscopy-based high-content analysis platform. Furthermore, this method can be similarly applied to other endocytic pathways if other fluorescent, pathway-specific, soluble markers are available.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Afinidade de Anticorpos / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Afinidade de Anticorpos / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article