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Magnetic nanoparticles--templated assembly of protein subunits: a new platform for carbohydrate-based MRI nanoprobes
- Publication Year :
- 2011
-
Abstract
- A new approach for the preparation of carbohydrate-coated magnetic nanoparticles is reported. In a first step, we show that the pH-driven assembly-disassembly natural process that occurs in apoferritin protein is effective for the encapsulation of maghemite nanoparticles of different sizes: 4 and 6 nm. In a second step, we demonstrate that the presence of functional amine groups in the outer shell of apoferritin allows functionalization with two carbohydrates, N-acetyl-D-glucosamine and d-mannose. High-resolution electron microscopy (HREM), high angle annular dark field scanning electron microscopy (HAADF-STEM), electron energy loss spectroscopy (EELS), X-ray diffraction (XRD), and SQUID technique have been used to characterize the magnetic samples, termed herein Apomaghemites. The in vivo magnetic resonance imaging (MRI) studies showed the efficiency in contrasting images for these samples; that is, the r(2) NMR relaxivities are comparable with Endorem (a commercial superparamagnetic MRI contrast agent). The r(2) relaxivity values as well as the pre-contrast and post-contrast T(2)*-weighted images suggested that our systems could be used as perspective superparamagnetic contrast agents for magnetic resonance imaging (MRI). The carbohydrate-functionalized Apomaghemite nanoparticles retained their recognition abilities, as demonstrated by the strong affinity with their corresponding carbohydrate-binding lectins.
- Subjects :
- Models, Molecular
Magnetic Resonance Spectroscopy
Surface Properties
Protein subunit
Carbohydrates
Nanotechnology
Crystallography, X-Ray
Biochemistry
Ferric Compounds
Catalysis
Magnetics
Contrast Agents
Colloid and Surface Chemistry
Lectins
Particle Size
Magnetic Nanoparticles
MRI
Chemistry
General Chemistry
Carbohydrate
Hydrogen-Ion Concentration
Magnetic Resonance Imaging
Protein Subunits
Apoferritins
Magnetic nanoparticles
Nanoparticles
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....dd01369ec4b5b485574d9e44ecfc865b