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首页> 外文期刊>ACS applied materials & interfaces >Oriented Bioconjugation of Unmodified Antibodies to Quantum Dots Capped with Copolymeric Ligands as Versatile Cellular Imaging Tools
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Oriented Bioconjugation of Unmodified Antibodies to Quantum Dots Capped with Copolymeric Ligands as Versatile Cellular Imaging Tools

机译:定向的生物修饰抗体与共轭配体作为多功能细胞成像工具的量子点的生物共轭。

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Distinctive optical properties of inorganic quantum dot (QD) nanoparticles promise highly valuable probes for fluorescence-based detection methods, particularly for in vivo diagnostics, cell phenotyping via multiple markers or single molecule tracking. However, despite high hopes, this promise has not been fully realized yet, mainly due to difficulties at producing stable, nontoxic QD bioconjugates of negligible nonspecific binding. Here, a universal platform for antibody binding to QDs is presented that builds upon the controlled functionalization of CdSe/CdS/ZnS nanoparticles capped with a multidentate dithiol/zwitterion copolymer ligand. In a change-of-paradigm approach, thiol groups are concomitantly used as anchoring and bioconjugation units to covalently bind up to 10 protein A molecules per QD while preserving their long-term colloidal stability. Protein A conjugated to QDs then enables the oriented, stoichiometrically controlled immobilization of whole, unmodified antibodies by simple incubation. This QD-protein A immobilization platform displays remarkable antibody functionality retention after binding, usually a compromised property in antibody conjugation to surfaces. Typical QD-protein A antibody assemblies contain about three fully functional antibodies. Validation experiments show that these nanobioconjugates overcome current limitations since they retain their colloidal stability and antibody functionality over 6 months, exhibit low nonspecific interactions with live cells and have very low toxicity: after 48 h incubation with 1 mu M QD bioconjugates, HeLa cells retain more than 80% of their cellular metabolism. Finally, these QD nanobioconjugates possess a high specificity for extra- and intracellular targets in live and fixed cells. The dithiol/zwitterion QD protein A nanoconjugates have thus a latent potential to become an off-the-shelf tool destined to unresolved biological questions.
机译:无机量子点(QD)纳米粒子的独特光学性能有望为基于荧光的检测方法,特别是体内诊断,通过多个标记物进行细胞表型鉴定或单分子跟踪的探针提供非常有价值的探针。然而,尽管抱有很高的希望,但这一承诺尚未完全实现,这主要是由于难以产生可忽略的非特异性结合的稳定,无毒的QD生物缀合物。在此,提出了一种抗体与QD结合的通用平台,该平台建立在以多齿二硫醇/两性离子共聚物配体封端的CdSe / CdS / ZnS纳米粒子的受控功能化基础上。在范式改变方法中,硫醇基团同时用作锚定和生物缀合单元,以共价键合每个QD最多10个蛋白质A分子,同时保留其长期胶体稳定性。然后,通过简单的孵育,与QD偶联的蛋白A可以对未修饰的完整抗体进行定向,化学计量控制的固定化。这种QD-蛋白A固定平台在结合后显示出显着的抗体功能保留,通常是抗体与表面结合的特性受损。典型的QD-蛋白A抗体组件包含约三种全功能抗体。验证实验表明,这些纳米生物共轭物克服了当前的局限性,因为它们在六个月内保留了其胶体稳定性和抗体功能,与活细胞的非特异性相互作用低,且毒性极低:与1μMQD生物共轭物孵育48小时后,HeLa细胞保留了更多超过其细胞新陈代谢的80%。最后,这些QD纳米生物共轭物对活细胞和固定细胞中的细胞外和细胞内靶标具有高度特异性。因此,二硫醇/两性离子QD蛋白A纳米偶联物具有潜在的潜力,可用于解决尚未解决的生物学问题的现成工具。

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