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用于高对比度免疫细胞化学的上转换纳米粒子的表面设计。

Surface design of photon-upconversion nanoparticles for high-contrast immunocytochemistry.

机构信息

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, 93053 Regensburg, Germany.

出版信息

Nanoscale. 2020 Apr 21;12(15):8303-8313. doi: 10.1039/c9nr10568a. Epub 2020 Apr 1.

Abstract

Immunohistochemistry (IHC) and immunocytochemistry (ICC) are routinely employed for the microscopic identification and diagnosis of cancerous cells in histological tissues and cell cultures. The maximally attainable contrast of conventional histological staining techniques, however, is low. While the anti-Stokes emission of photon-upconversion nanoparticles (UCNP) can efficiently eliminate optical background interference, excluding non-specific interactions of the label with the histological sample is equally important for specific immunolabeling. To address both requirements, we have designed and characterized several UCNP-based nanoconjugates as labels for the highly specific detection of the cancer biomarker HER2 on various breast cancer cell lines. An optimized streptavidin-PEG-neridronate-UCNP conjugate provided an unsurpassed signal-to-background ratio of 319, which was 50-fold better than conventional fluorescent labeling under the same experimental conditions. In combination, the absence of optical interference and non-specific binding lays the foundation for computer-based data evaluation in digital pathology.

摘要

免疫组织化学(IHC)和免疫细胞化学(ICC)常用于组织学和细胞培养物中癌细胞的微观鉴定和诊断。然而,传统组织学染色技术的最大对比度较低。虽然上转换纳米粒子(UCNP)的反斯托克斯发射可以有效地消除光学背景干扰,但排除标签与组织样本的非特异性相互作用对于特异性免疫标记同样重要。为了满足这两个要求,我们设计并表征了几种基于 UCNP 的纳米复合物作为标记物,用于高度特异性地检测各种乳腺癌细胞系上的癌症生物标志物 HER2。优化的链霉亲和素-PEG-奈立膦酸-UCNP 缀合物提供了无与伦比的 319 的信号背景比,在相同的实验条件下比传统荧光标记好 50 倍。结合起来,光学干扰和非特异性结合的缺失为数字病理学中的基于计算机的数据评估奠定了基础。

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