Evidence for electro-induced membrane defects assessed by lateral mobility measurement of a GPi anchored protein

Eur Biophys J. 2014 Jul;43(6-7):277-86. doi: 10.1007/s00249-014-0961-1. Epub 2014 Apr 30.

Abstract

Electrotransfer is a method by which molecules can be introduced into living cells via plasma membrane electropermeabilization. Here, we show that electropermeabilization affects the lateral mobility of Rae-1, a GPi anchored protein. Our results suggest that 10-20 % of the membrane surface is occupied by defects or pores and that these structures propagate rapidly (<1 min) over the cell surface. Electrotransfer of plasmid DNA (pDNA) also affects the lateral mobility of Rae-1. Furthermore, we clearly show that, once inserted into the plasma membrane, pDNA is completely immobile and excludes Rae-1; this indicates that the pDNA molecules are tightly packed together to form aggregates occupying at least the outer leaflet of the plasma membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cell Membrane / metabolism*
  • Cricetinae
  • Cricetulus
  • DNA / metabolism
  • Electroporation*
  • Nucleocytoplasmic Transport Proteins / metabolism*
  • Plasmids / genetics
  • Porosity

Substances

  • Nucleocytoplasmic Transport Proteins
  • DNA