Phage Display Breast Carcinoma cDNA Libraries: Isolation of Clones Which Specifically Bind to Membrane Glycoproteins, Mucins, and Endothelial Cell Surface

Abstract

Approved tor public release; distribution unlimited 13. ABSTRACT (Maximum 200 Words) We proposed to identify%, by using a novel phage display technique, carbohydrate-binding proteins (lectins), which may play an important role in progression and metastasis of breast cancer. Using blood- group H-expressing glycoprotein fraction as bait, we observed enrichment of phage clones expressing sequences from galectin-3, a lectin with an affinity with the blood-group substance. Since we obtained a multiple number of different clones encoding this protein, the binding was selective and real. We then constructed additional libraries including MCF-7 human breast carcinoma and EJG bovine capillary endothelial cell libraries. We performed in vitro biopanning experiments using as bait purified fractions of glycoproteins and glycolipids, as well as antibodies against plant lectins, and obtained several dozens of candidate phage clones.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2000
Accession Number
ADA389517

Entities

People

  • Fumiichiro Yamamoto

Organizations

  • Sanford Burnham Prebys Medical Discovery Institute

Tags

DTIC Thesaurus Topics

  • Biomedical And Dental Materials
  • Blood
  • Blood Groups
  • Breast Cancer
  • Carbohydrates
  • Carrier Proteins
  • Cells
  • Cellular Structures
  • Chemistry
  • Endothelial Cells
  • Genetic Code
  • Genetic Structures
  • Glycoproteins
  • Medical Personnel
  • Molecules
  • Polymeric Films
  • Proteins

Fields of Study

  • Biology

Readers

  • Immunology
  • Molecular Genetics
  • Oncology (Cancer Research).