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评估连接到上转换纳米颗粒的抗体的免疫标记活性。

Assessing the activity of antibodies conjugated to upconversion nanoparticles for immunolabeling.

机构信息

ARC Centre of Excellence for Nanoscale Biophotonics (CNBP), Australia; Department of Molecular Sciences, Macquarie University, Sydney, NSW, Australia.

Minomic International Ltd, Talavera Road, Macquarie Park, Australia.

出版信息

Anal Chim Acta. 2022 May 29;1209:339863. doi: 10.1016/j.aca.2022.339863. Epub 2022 Apr 23.

Abstract

Surface modification and functionalization is typically required to engineer upconversion nanoparticles (UCNPs) for biosensing and bioimaging applications. Nevertheless, despite various antibody conjugation methods having been applied to UCNPs, no consensus has been reached on the best choice, as the results from individual studies are largely unable to be compared due to inadequate assessment of the properties of the conjugated products. Here, we introduce a systematic approach to quantitatively evaluate the biological activity of antibody-conjugated UCNPs. We determine that the optimal antibody conjugation efficiency to our colominic acid polysaccharide-coated UCNPs via 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide/N-hydroxy succinimide (EDC/NHS) coupling is approximately 70%, corresponding to 16 antibodies per nanoparticle of 63 nm hydrodynamic diameter, with on average 12 of the 16 antibodies maintaining their affinity to the target antigens. The binding ability of the antibody-conjugated UCNPs to the antigen was well preserved, as verified by enzyme-linked immunosorbent assay (ELISA), flow cytometry, and cellular imaging. This is the first study to quantitate the active antibody binding capacity of polysaccharide coated UCNP nanoparticles, offering a practical guideline for benchmarking functionalised UCNPs in future studies.

摘要

表面修饰和功能化通常是工程上需要的上转换纳米粒子 (UCNPs) 的生物传感和生物成像应用。尽管已经应用了各种抗体偶联方法于 UCNPs,但由于对共轭产物性质的评估不足,因此尚未就最佳选择达成共识,因为个别研究的结果在很大程度上无法进行比较。在这里,我们介绍了一种定量评估抗体偶联 UCNPs 的生物学活性的系统方法。我们确定,通过 1-乙基-3-(3-二甲基氨基丙基)碳二亚胺/N-羟基琥珀酰亚胺 (EDC/NHS) 偶联,我们的 colominic 酸多糖包覆的 UCNPs 的最佳抗体偶联效率约为 70%,对应于每个 63nm 水动力直径的纳米粒子有 16 个抗体,平均每个抗体有 12 个抗体保持其对目标抗原的亲和力。抗体偶联的 UCNPs 与抗原的结合能力得到了很好的保留,通过酶联免疫吸附测定 (ELISA)、流式细胞术和细胞成像进行了验证。这是首次定量测定多糖包覆 UCNP 纳米粒子的活性抗体结合能力的研究,为未来研究中功能化 UCNPs 的基准测试提供了实用的指导方针。

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