荧光团
化学
人血清白蛋白
费斯特共振能量转移
荧光
荧光相关光谱
全内反射荧光显微镜
荧光光谱法
纳米颗粒
光谱学
量子点
纳米材料
生命科学中的荧光
表面等离子共振
分析化学(期刊)
光化学
纳米技术
材料科学
分子
有机化学
色谱法
膜
物理
量子力学
生物化学
作者
Lianxun Gao,Hao Hao,Ying-Qi Yu,Jilei Chen,Wenqi Chen,Zuo-Dong Gong,Yi Liu,Feng‐Lei Jiang
出处
期刊:Langmuir
[American Chemical Society]
日期:2023-10-18
卷期号:39 (43): 15275-15284
被引量:6
标识
DOI:10.1021/acs.langmuir.3c01986
摘要
Once nanoparticles enter into the biological milieu, nanoparticle-biomacromolecule complexes, especially the protein corona, swiftly form, which cause obvious effects on the physicochemical properties of both nanoparticles and proteins. Here, the thermodynamic parameters of the interactions between water-soluble GSH-CdSe/ZnS core/shell quantum dots (GSH-QDs) and human serum albumin (HSA) were investigated with the aid of labeling fluorescence of HSA. It was proved that the labeling fluorescence originating from a fluorophore (BDP-CN for instance) could be used to investigate the interactions between QDs and HSA. Gel electrophoresis displayed that the binding ratio between HSA and QDs was ∼2:1 by direct visualization. Fluorescence resonance energy transfer (FRET) results indicated that the distance between the QDs and the fluorophore BDP-CN in HSA was 7.2 nm, which indicated that the distance from the fluorophore to the surface of the QDs was ∼4.8 nm. Fluorescence correlation spectroscopy (FCS) results showed that HSA formed a monolayer of a protein corona with a thickness of 5.5 nm. According to the spatial structure of HSA, we could speculate that the binding site of QDs was located at the side edge (not the triangular plane) of HSA with an equilateral triangular prism. The elaboration of the thermodynamic parameters, binding ratio, and interaction orientation will highly improve the fundamental understanding of the formation of protein corona. This work has guiding significance for the exploration of the interactions between proteins and nanomaterials.
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