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用于细胞靶点免疫荧光标记的量子点偶联抗体的评估。

Evaluation of quantum dot conjugated antibodies for immunofluorescent labelling of cellular targets.

作者信息

Francis Jennifer E, Mason David, Lévy Raphaël

机构信息

Department of Biochemistry, Institute of Integrative Biology, Biosciences Building, Crown Street, Liverpool, L69 7ZB, United Kingdom.

Centre for Cell Imaging, Institute of Integrative Biology, Biosciences Building, Crown Street, Liverpool, L69 7ZB, United Kingdom.

出版信息

Beilstein J Nanotechnol. 2017 Jun 9;8:1238-1249. doi: 10.3762/bjnano.8.125. eCollection 2017.

Abstract

Semiconductor quantum dots (Qdots) have been utilised as probes in fluorescence microscopy and provide an alternative to fluorescent dyes and fluorescent proteins due to their brightness, photostability, and the possibility to excite different Qdots with a single wavelength. In spite of these attractive properties, their implemenation by biologists has been somewhat limited and only a few Qdot conjugates are commercially available for the labelling of cellular targets. Although many protocols have been reported for the specific labelling of proteins with Qdots, the majority of these relied on Qdot-conjugated antibodies synthesised specifically by the authors (and therefore not widely available), which limits the scope of applications and complicates replication. Here, the specificity of a commercially available, Qdot-conjugated secondary antibody (Qdot-Ab) was tested against several primary IgG antibodies. The antigens were labelled simultaneously with a fluorescent dye coupled to a secondary antibody (Dye-Ab) and the Qdot-Ab. Although, the Dye-Ab labelled all of the intended target proteins, the Qdot-Ab was found bound to only some of the protein targets in the cytosol and could not reach the nucleus, even after extensive cell permeabilisation.

摘要

半导体量子点(Qdots)已被用作荧光显微镜中的探针,由于其亮度、光稳定性以及能用单一波长激发不同量子点的可能性,它为荧光染料和荧光蛋白提供了一种替代方案。尽管具有这些吸引人的特性,但生物学家对它们的应用在一定程度上受到限制,只有少数量子点偶联物可用于细胞靶点标记的商业化产品。虽然已经报道了许多用量子点特异性标记蛋白质的方案,但其中大多数依赖于作者专门合成的量子点偶联抗体(因此无法广泛获取),这限制了应用范围并使重复实验变得复杂。在此,测试了一种市售的量子点偶联二抗(Qdot - Ab)针对几种一抗IgG的特异性。用与二抗偶联的荧光染料(Dye - Ab)和Qdot - Ab同时标记抗原。尽管Dye - Ab标记了所有预期的靶蛋白,但发现Qdot - Ab仅与细胞质中的一些蛋白靶点结合,即使在进行广泛的细胞通透处理后也无法进入细胞核。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b2/5480344/2c17722e7cc9/Beilstein_J_Nanotechnol-08-1238-g002.jpg

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