Adsorption and Unfolding of a Single Protein Triggers Nanoparticle Aggregation
Author(s) -
Sergio Domínguez-Medina,
Lydia Kisley,
Lawrence J. Tauzin,
Anneli Hoggard,
Bo Shuang,
Agampodi S. De Silva Indrasekara,
Sishan Chen,
Lin-Yung Wang,
Paul J. Derry,
Anton V. Liopo,
Eugene R. Zubarev,
Christy F. Landes,
Stephan Link
Publication year - 2016
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.5b06439
Subject(s) - nanoparticle , biophysics , nanotechnology , nanorod , in vivo , bovine serum albumin , chemistry , colloidal gold , protein aggregation , particle (ecology) , protein adsorption , materials science , adsorption , biology , biochemistry , ecology , microbiology and biotechnology , organic chemistry
The response of living systems to nanoparticles is thought to depend on the protein corona, which forms shortly after exposure to physiological fluids and which is linked to a wide array of pathophysiologies. A mechanistic understanding of the dynamic interaction between proteins and nanoparticles and thus the biological fate of nanoparticles and associated proteins is, however, often missing mainly due to the inadequacies in current ensemble experimental approaches. Through the application of a variety of single molecule and single particle spectroscopic techniques in combination with ensemble level characterization tools, we identified different interaction pathways between gold nanorods and bovine serum albumin depending on the protein concentration. Overall, we found that local changes in protein concentration influence everything from cancer cell uptake to nanoparticle stability and even protein secondary structure. We envision that our findings and methods will lead to strategies to control the associated pathophysiology of nanoparticle exposure in vivo.
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