Quantitative study of protein coronas on gold nano- particles with different surface modifications

Protein coronas provide the biological identity of nanomaterials in vivo. Here we have used dynamic light scattering （DLS） and transmission electron microscopy （TEM） to investigate the adsorption of serum proteins, including bovine serum albumin （BSA）, transferrin （TRF） and fibrinogen （FIB）, on gold...

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Published in纳米研究：英文版 no. 3; pp. 345 - 352
Main Author Menghua Cui Renxiao Liu Zhaoyi Deng Guanglu Ge Ying Liu Liming Xie
Format Journal Article
LanguageEnglish
Published 2014
Subjects
柠檬酸盐
牛血清白蛋白
电晕
纤维蛋白原
蛋白质
表面修饰
透射电子显微镜
金纳米粒子
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Summary:Protein coronas provide the biological identity of nanomaterials in vivo. Here we have used dynamic light scattering （DLS） and transmission electron microscopy （TEM） to investigate the adsorption of serum proteins, including bovine serum albumin （BSA）, transferrin （TRF） and fibrinogen （FIB）, on gold nanoparticles （AuNPs） with different surface modifications （citrate, thioglycolic acid, cysteine, polyethylene glycol （PEG, Mw = 2 k and 5 k））. AuNPs with PEG（5 k） surface modification showed no protein adsorption. AuNPs with non-PEG surface modifications showed aggregation with FIB. AuNPs with citrate and thioglycolic acid surface modifications showed 6-8 nm thick BSA and TRF coronas （corres- ponding to monolayer or bilayer proteins）, in which the microscopic dissociation constants of BSA and TRF protein coronas are in the range of 104 to 104 M.
Bibliography:Protein coronas provide the biological identity of nanomaterials in vivo. Here we have used dynamic light scattering （DLS） and transmission electron microscopy （TEM） to investigate the adsorption of serum proteins, including bovine serum albumin （BSA）, transferrin （TRF） and fibrinogen （FIB）, on gold nanoparticles （AuNPs） with different surface modifications （citrate, thioglycolic acid, cysteine, polyethylene glycol （PEG, Mw = 2 k and 5 k））. AuNPs with PEG（5 k） surface modification showed no protein adsorption. AuNPs with non-PEG surface modifications showed aggregation with FIB. AuNPs with citrate and thioglycolic acid surface modifications showed 6-8 nm thick BSA and TRF coronas （corres- ponding to monolayer or bilayer proteins）, in which the microscopic dissociation constants of BSA and TRF protein coronas are in the range of 104 to 104 M.
11-5974/O4
protein corona,gold nanoparticle,dynamic light scattering,transmission electronmicroscopy,surface modification
ISSN:1998-0124
1998-0000