4.6 Article

Thermodynamics and Mechanisms of the Interactions between Ultrasmall Fluorescent Gold Nanoclusters and Human Serum Albumin, γ-Globulins, and Transferrin: A Spectroscopic Approach

Journal

LANGMUIR
Volume 33, Issue 21, Pages 5108-5116

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.7b00196

Keywords

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Funding

  1. National Natural Science Foundation of China [21573168, 21303126, 21473125]
  2. Bagui Scholar Program of Guangxi Province
  3. Natural Science Foundation of Hubei Province [2014CFA003]
  4. Large-scale Instrument and Equipment Sharing Foundation of Wuhan University

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Noble metal nanoclusters (NCs) show great promise as nanoprobes for bioanalysis and cellular imaging in biological applications due to ultrasmall size, good photophysical properties, and excellent biocompatibility. In order to achieve a comprehensive understanding of possible biological implications, a series of spectroscopic measurements were conducted under different temperatures to investigate the interactions of Au NCs (similar to 1.7 nm) with three model plasmatic proteins (human serum albumin (HSA), gamma-globulins, and transferrin). It was found that the fluorescence quenching of HSA and gamma-globulins triggered by Au NCs was due to dynamic quenching mechanism, while the fluorescence quenching of transferrin by Au NCs was a result of the formation of a Au NC-transferrin complex. The apparent association constants of the Au NCs bound to HSA, gamma-globulins, and transferrin demonstrated no obvious difference. Thermodynamic studies demonstrates that the interaction between Au NCs and HSA (or gamma-globulins) was driven by hydrophobic forces, while the electrostatic interactions played predominant roles in the adsorption process for transferrin. Furthermore, it was proven that Au NCs had no obvious interference in the secondary structures of these three kinds of proteins. In turn, these three proteins had a minor effect on the fluorescence intensity of Au NCs, which made fluorescent Au Ncs promising in biological applications owing to their chemical and photophysical stability. In addition, by comparing the interactions of small molecules, Au NCs, and large nanomaterials with serum albumin, it was found that the binding constants were gradually increased with the increase of particle size. This work has elucidated the interaction mechanisms between nanoclusters and proteins, and shed light on a new interaction mode different from the protein corona on the surface of nanoparticles, which will highly contribute to the better design and applications of fluorescent nanoclusters.

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