Literature DB >> 16552091

Detecting cryptic epitopes created by nanoparticles.

Iseult Lynch1, Kenneth A Dawson, Sara Linse.   

Abstract

As potential applications of nanotechnology and nanoparticles increase, so too does the likelihood of human exposure to nanoparticles. Because of their small size, nanoparticles are easily taken up into cells (by receptor-mediated endocytosis), whereupon they have essentially free access to all cellular compartments. Similarly to macroscopic biomaterial surfaces (that is, implants), nanoparticles become coated with a layer of adsorbed proteins immediately upon contact with physiological solutions (unless special efforts are taken to prevent this). The process of adsorption often results in conformational changes of the adsorbed protein, which may be affected by the larger curvature of nanoparticles compared with implant surfaces. Protein adsorption may result in the exposure at the surface of amino acid residues that are normally buried in the core of the native protein, which are recognized by the cells as "cryptic epitopes." These cryptic epitopes may trigger inappropriate cellular signaling events (as opposed to being rejected by the cells as foreign bodies). However, identification of such surface-exposed epitopes is nontrivial, and the molecular nature of the adsorbed proteins should be investigated using biological and physical science methods in parallel with systems biology studies of the induced alterations in cell signaling.

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Year:  2006        PMID: 16552091     DOI: 10.1126/stke.3272006pe14

Source DB:  PubMed          Journal:  Sci STKE        ISSN: 1525-8882


  51 in total

1.  An index for characterization of nanomaterials in biological systems.

Authors:  Xin-Rui Xia; Nancy A Monteiro-Riviere; Jim E Riviere
Journal:  Nat Nanotechnol       Date:  2010-08-15       Impact factor: 39.213

2.  Exposure to nanoparticles and hormesis.

Authors:  Ivo Iavicoli; Edward J Calabrese; Marc A Nascarella
Journal:  Dose Response       Date:  2010-08-12       Impact factor: 2.658

3.  Understanding the nanoparticle-protein corona using methods to quantify exchange rates and affinities of proteins for nanoparticles.

Authors:  Tommy Cedervall; Iseult Lynch; Stina Lindman; Tord Berggård; Eva Thulin; Hanna Nilsson; Kenneth A Dawson; Sara Linse
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-31       Impact factor: 11.205

Review 4.  Probing the interactions of proteins and nanoparticles.

Authors:  Jacob Klein
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-06       Impact factor: 11.205

Review 5.  The effects of nanomaterials as endocrine disruptors.

Authors:  Ivo Iavicoli; Luca Fontana; Veruscka Leso; Antonio Bergamaschi
Journal:  Int J Mol Sci       Date:  2013-08-14       Impact factor: 5.923

Review 6.  Exploiting endocytosis for nanomedicines.

Authors:  Akin Akinc; Giuseppe Battaglia
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-11-01       Impact factor: 10.005

7.  Pulsed-laser creation and characterization of giant plasma membrane vesicles from cells.

Authors:  Christopher V Kelly; Mary-Margaret T Kober; Päivö Kinnunen; David A Reis; Bradford G Orr; Mark M Banaszak Holl
Journal:  J Biol Phys       Date:  2009-06-20       Impact factor: 1.365

8.  Protein-nanoparticle interactions: What does the cell see?

Authors:  Iseult Lynch; Anna Salvati; Kenneth A Dawson
Journal:  Nat Nanotechnol       Date:  2009-09       Impact factor: 39.213

9.  Amyloid fibril length distribution quantified by atomic force microscopy single-particle image analysis.

Authors:  Wei-Feng Xue; Steve W Homans; Sheena E Radford
Journal:  Protein Eng Des Sel       Date:  2009-07-06       Impact factor: 1.650

10.  Fibril fragmentation enhances amyloid cytotoxicity.

Authors:  Wei-Feng Xue; Andrew L Hellewell; Walraj S Gosal; Steve W Homans; Eric W Hewitt; Sheena E Radford
Journal:  J Biol Chem       Date:  2009-10-06       Impact factor: 5.157

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