单宁酸
纳米颗粒
抗体
物理吸附
抗原
水溶液中的金属离子
材料科学
化学
纳米晶
纳米技术
生物物理学
钴
金属
组合化学
催化作用
生物化学
无机化学
有机化学
生物
免疫学
遗传学
作者
Wenjie Zhang,Quinn A. Besford,Andrew J. Christofferson,Patrick Charchar,Joseph J. Richardson,Aaron Elbourne,Kristian Kempe,Christoph E. Hagemeyer,Matthew R. Field,C. F. McConville,Irene Yarovsky,Frank Caruso
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-03-10
卷期号:20 (4): 2660-2666
被引量:73
标识
DOI:10.1021/acs.nanolett.0c00295
摘要
The orientation-specific immobilization of antibodies onto nanoparticles, to preserve antibody–antigen recognition, is a key challenge in developing targeted nanomedicines. Herein, we report the targeting ability of metal–phenolic network (MPN)-coated gold nanoparticles with surface-physisorbed antibodies against respective antigens. The MPN coatings were self-assembled from metal ions (Fe III, Co II, Cu II, Ni II, or Zn II ) cross-linked with tannic acid. Upon physisorption of antibodies, all particle systems exhibited enhanced association with target antigens, with Co II systems demonstrating more than 2-fold greater association. These systems contained more metal atoms distributed in a way to specifically interact with antibodies, which were investigated by molecular dynamics simulations. A model antibody fragment crystallizable (Fc) region in solution with Co II -tannic acid complexes revealed that the solvent-exposed Co II can directly coordinate to the histidine-rich portion of the Fc region. This one-pot interaction suggests anchoring of the antibody Fc region to the MPN on nanoparticles, allowing for enhanced targeting.
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