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Specific functionalization of CTAB stabilized anisotropic gold nanoparticles with polypeptides for folding-mediated self-assembly

机译:CTAB稳定的各向异性金纳米粒子与多肽的特异性功能化,用于折叠介导的自组装

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摘要

Anisotropic nanoparticles stabilized by cetyltrimethylammonium bromide (CTAB) are notoriously difficult to homogenously functionalize using conventional gold-thiol chemistry. Using surface assisted laser desorption time of flight mass spectroscopy and scanning transmission electron microscopy-energy dispersive X-ray spectroscopy, we demonstrate that silver species adsorbed on the particle surface prevent effective surface functionalization. When covered by a thin gold film, particle functionalization was drastically improved. A thiol-containing polypeptide was immobilized on arrowhead gold nanorods (NRs) and was subsequently able to selectively heteroassociate with a complementary polypeptide resulting in a folding-mediated bridging aggregation of the NRs. Despite using arrowhead NRs with a pronounced difference in surface arrangement on the {111} facets on the arrowheads compared to the {100} facets at the particle sides, the polypeptides were efficiently and homogeneously immobilized on the particles after gold film overgrowth.
机译:众所周知,用十六烷基三甲基溴化铵(CTAB)稳定的各向异性纳米粒子很难使用常规的金硫醇化学方法进行均相功能化。使用表面辅助激光解吸飞行时间质谱仪和扫描透射电子显微镜-能量色散X射线光谱仪,我们证明了颗粒表面吸附的银物质阻止了有效的表面功能化。当被薄的金膜覆盖时,颗粒的功能化得到了极大的改善。含硫醇的多肽固定在箭头金纳米棒(NRs)上,随后能够与互补多肽选择性地异缔合,从而导致NRs的折叠介导桥联聚集。尽管使用的箭头NR与粒子侧面的{100}平面相比,箭头的{111}平面在箭头上的表面排列存在明显差异,但是多肽在金膜过度生长后被有效且均匀地固定在粒子上。

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