Understanding and controlling the interaction of nanomaterials with proteins in a physiological environment
Top Cited Papers
- 15 November 2011
- journal article
- review article
- Published by Royal Society of Chemistry (RSC) in Chemical Society Reviews
- Vol. 41 (7), 2780-2799
- https://doi.org/10.1039/c1cs15233e
Abstract
Nanomaterials hold promise as multifunctional diagnostic and therapeutic agents. However, the effective application of nanomaterials is hampered by limited understanding and control over their interactions with complex biological systems. When a nanomaterial enters a physiological environment, it rapidly adsorbs proteins forming what is known as the protein ‘corona’. The protein corona alters the size and interfacial composition of a nanomaterial, giving it a biological identity that is distinct from its synthetic identity. The biological identity determines the physiological response including signalling, kinetics, transport, accumulation, and toxicity. The structure and composition of the protein corona depends on the synthetic identity of the nanomaterial (size, shape, and composition), the nature of the physiological environment (blood, interstitial fluid, cell cytoplasm, etc.), and the duration of exposure. In this critical review, we discuss the formation of the protein corona, its structure and composition, and its influence on the physiological response. We also present an ‘adsorbome’ of 125 plasma proteins that are known to associate with nanomaterials. We further describe how the protein corona is related to the synthetic identity of a nanomaterial, and highlight efforts to control protein–nanomaterial interactions. We conclude by discussing gaps in the understanding of protein–nanomaterial interactions along with strategies to fill them (167 references).Keywords
This publication has 162 references indexed in Scilit:
- Effect of gold nanoparticle morphology on adsorbed protein structure and functionBiomaterials, 2011
- Stabilization of Magnetic Iron Oxide Nanoparticles in Biological Media by Fetal Bovine Serum (FBS)Langmuir, 2010
- Serum heat inactivation affects protein corona composition and nanoparticle uptakeBiomaterials, 2010
- Stealth nanoparticles: High density but sheddable PEG is a key for tumor targetingJournal of Controlled Release, 2010
- Differential proteomics analysis of the surface heterogeneity of dextran iron oxide nanoparticles and the implications for their in vivo clearanceBiomaterials, 2009
- Interaction of colloidal gold nanoparticles with human blood: effects on particle size and analysis of plasma protein binding profilesNanomedicine: Nanotechnology, Biology and Medicine, 2008
- Foreign body reaction to biomaterialsSeminars in Immunology, 2007
- Formulation of functionalized PLGA–PEG nanoparticles for in vivo targeted drug deliveryBiomaterials, 2006
- Erratum to “The role of apolipoprotein E in the elimination of liposomes from blood by hepatocytes in the mouse” [Biochem. Biophys. Res. Commun. 328 (2005) 57–62]Biochemical and Biophysical Research Communications, 2005
- Non-phagocytic uptake of intravenously injected microspheres in rat spleen: Influence of particle size and hydrophilic coatingBiochemical and Biophysical Research Communications, 1991