Immobilization of histidine-tagged proteins by magnetic nanoparticles encapsulated with nitrilotriacetic acid (NTA)-phospholipids micelle

Biochem Biophys Res Commun. 2006 Jun 9;344(3):926-30. doi: 10.1016/j.bbrc.2006.03.209. Epub 2006 Apr 19.

Abstract

We described the development of functionalized magnetic nanoparticles (MNPs) with PEG-modification, a phospholipids micelle coating, and their use in manipulating histidine-tagged proteins. Highly monodisperse MNPs were synthesized in an organic solvent and could be phase-transferred into an aqueous solution by encapsulating the nanoparticles with a phospholipids micelle. The phospholipids micelle coating rendered the nanoparticles highly water-soluble, and the functional groups of the phospholipids coating allowed for the bioconjugation of various moieties, such as fluorescent molecules and engineered proteins. Functionalized phospholipids, such as nitrilotriacetic acid (NTA)-phospholipids, caused the MNPs to bind and allowed for manipulation of histidine-tagged proteins. Due to their high surface/volume ratio, the MNPs showed better performance (about 100 times higher) in immobilizing engineered proteins than conventional micrometer-sized beads. This demonstrates that MNPs coated with phospholipids micelle can be a versatile platform for the effective manipulation of various kinds of engineered proteins, which is very important in the field of proteomics. It is expected that a combination of MNPs with optical fluorescent molecules can find applications in bimodal (magnetic and optical) molecular imaging nanoprobes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coated Materials, Biocompatible / chemistry
  • Coated Materials, Biocompatible / radiation effects
  • Histidine / chemistry*
  • Histidine / radiation effects
  • Magnetics*
  • Micelles
  • Motion
  • Nanostructures / chemistry*
  • Nanostructures / radiation effects
  • Nanostructures / ultrastructure*
  • Nitrilotriacetic Acid / chemistry*
  • Phospholipids / chemistry*
  • Recombinant Proteins / chemistry*
  • Recombinant Proteins / radiation effects
  • Recombinant Proteins / ultrastructure

Substances

  • Coated Materials, Biocompatible
  • Micelles
  • Phospholipids
  • Recombinant Proteins
  • Histidine
  • Nitrilotriacetic Acid