Surfection: a new platform for transfected cell arrays

Nucleic Acids Res. 2004 Feb 18;32(3):e33. doi: 10.1093/nar/gnh029.

Abstract

Efficient high-throughput expression of genes in mammalian cells can facilitate large-scale functional genomic studies. Towards this aim, we developed a simple yet powerful method to deliver genes into cells by cationic polymers on the surface of substrates. Transfection can be achieved by directly contacting nucleic acid-cell mixtures with the cationic substrates, e.g. polyethylenimine/collagen-coated wells. This single-step matrix-surface- mediated transfection method, termed 'surfection', can efficiently deliver multiple plasmids into cells and can successfully assay siRNA-mediated gene silencing. This technology represents the easiest method to transfer combinations of genes in large-scale arrays, and is a versatile tool for live-cell imaging and cell-based drug screening.

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Cell Line
  • Cell Line, Tumor
  • Collagen / chemistry
  • DNA / chemistry
  • DNA / genetics
  • Green Fluorescent Proteins
  • Humans
  • Luciferases / genetics
  • Luciferases / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Nerve Tissue Proteins / genetics
  • Phosphoproteins / genetics
  • Plasmids / chemistry
  • Plasmids / genetics
  • Polyethyleneimine / chemistry
  • RNA / chemistry
  • RNA / genetics
  • RNA Interference
  • RNA-Binding Proteins
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Transfection / instrumentation
  • Transfection / methods*

Substances

  • Carrier Proteins
  • EBNA1BP2 protein, human
  • Luminescent Proteins
  • Nerve Tissue Proteins
  • Phosphoproteins
  • RNA-Binding Proteins
  • Recombinant Fusion Proteins
  • collapsin response mediator protein-1
  • Green Fluorescent Proteins
  • RNA
  • Polyethyleneimine
  • Collagen
  • DNA
  • Luciferases