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Single-Pot Biofabrication of Zinc Sulfide Immuno-Quantum Dots

机译:硫化锌免疫量子点的单罐生物制造

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摘要

Quantum dots (QDs) are a powerful alternative to organic dyes and fluorescent proteins for biological and biomedical applications. These semiconductor nanocrystals are traditionally synthesized above 200 ℃ in organic solvents using toxic and costly precursors, and further steps are required to conjugate them to a biological ligand. Here, we describe a simple, aqueous route for the one-pot synthesis of antibody-derivatized zinc sulfide (ZnS) immuno-QDs. In this strategy, easily expressed and purified fusion proteins perform the dual function of nanocrystal mineralizers through ZnS binding sequences identified by cell surface display and adaptors for immunoglobin G (IgG) conjugation through a tandem repeat of the B domain of Staphylococcus aureus protein A. Although ≈4.3 nm ZnS wurtzite cores could be biomineralized from either zinc chloride or zinc acetate precursors, only the latter salt gives rise to protein-coated QDs with long shelf life and narrow hydrodynamic diameters (8.8 ± 1.4 nm). The biofabricated QDs have a quantum yield of 2.5% and blue-green ensemble emission with contributions from the band-edge at 340 nm and from trap states at 460 and 665 nm that are influenced by the identity of the protein shell. Murine IgG_1 antibodies exhibit high affinity (K_d = 60 nM) for the protein shell, and stable immuno-QDs with a hydrodynamic diameter of 14.1 ± 1.3 nm are readily obtained by mixing biofabricated nanocrystals with human IgG.
机译:对于生物和生物医学应用,量子点(QD)是有机染料和荧光蛋白的强大替代品。传统上,这些半导体纳米晶体是在200℃以上的有机溶剂中使用有毒且价格昂贵的前体合成的,需要进一步的步骤才能将它们与生物配体结合。在这里,我们描述了一种简单的水性途径,用于一锅合成抗体衍生的硫化锌(ZnS)免疫QD。在这种策略中,易于表达和纯化的融合蛋白通过细胞表面展示鉴定的ZnS结合序列和通过金黄色葡萄球菌蛋白A的B结构域的串联重复的免疫球蛋白G(IgG)缀合的衔接子执行纳米晶体矿化剂的双重功能。 ≈4.3nm的ZnS纤锌矿型芯可以从氯化锌或醋酸锌的前体中生物矿化,只有后者的盐才能产生具有长保质期和窄流体动力学直径(8.8±1.4 nm)的蛋白包被的量子点。生物制造的量子点具有2.5%的量子产率和蓝绿色系综发射,其受340 nm的能带边缘以及460和665 nm的陷阱态的影响,受蛋白质壳的特性影响。鼠IgG_1抗体对蛋白质壳表现出高亲和力(K_d = 60 nM),并且通过将生物制备的纳米晶体与人IgG混合,可以轻松获得具有14.1±1.3 nm流体力学直径的稳定免疫QD。

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  • 来源
    《Journal of the American Chemical Society》 |2010年第13期|p.4731-4738|共8页
  • 作者单位

    Department of Chemical Engineering, University of Washington, Box 351750, Seattle, Washington 98195;

    Department of Chemical Engineering, University of Washington, Box 351750, Seattle, Washington 98195;

    Department of Chemical Engineering, University of Washington, Box 351750, Seattle, Washington 98195;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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