Deparment of Physical and Analytical Chemistry, University of Oviedo, Julian Claveria 8, 33006, Oviedo, Spain.
Instituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, Universidad de Oviedo, Oviedo, Spain.
Mikrochim Acta. 2017 Dec 18;185(1):64. doi: 10.1007/s00604-017-2597-1.
An immunohistochemical method is described to visualize the distribution of metallothioneins 1/2 (MT 1/2) and metallothionein 3 (MT 3) in human ocular tissue. It is making use of (a) antibodies conjugated to gold nanoclusters (AuNCs) acting as labels, and (b) laser ablation (LA) coupled to inductively coupled plasma - mass spectrometry (ICP-MS). Water-soluble fluorescent AuNCs (with an average size of 2.7 nm) were synthesized and then conjugated to antibody by carbodiimide coupling. The surface of the modified AuNCs was then blocked with hydroxylamine to avoid nonspecific interactions with biological tissue. Immunoassays for MT 1/2 and MT 3 in ocular tissue sections (5 μm thick) from two post mortem human donors were performed. Imaging studies were then performed by fluorescence using confocal microscopy, and LA-ICP-MS was performed in the retina to measure the signal for gold. Signal amplification by the >500 gold atoms in each nanocluster allowed the antigens (MT 1/2 and MT 3) to be imaged by LA-ICP-MS using a laser spot size as small as 4 μm. The image patterns found in retina are in good agreement with those obtained by conventional fluorescence immunohistochemistry which was used as an established reference method. Graphical abstract Gold nanoclusters (AuNCs) conjugated to a primary specific antibody serve as a label for amplified bioimaging of metallothioneins (MTs) by laser ablation coupled to inductively coupled plasma - mass spectrometry (ICP-MS) in human ocular tissue sections.
本文描述了一种免疫组织化学方法,用于可视化金属硫蛋白 1/2 (MT 1/2) 和金属硫蛋白 3 (MT 3) 在人眼组织中的分布。它利用(a)与金纳米簇 (AuNCs) 结合的抗体作为标记,以及(b)与电感耦合等离子体质谱 (ICP-MS) 耦合的激光烧蚀 (LA)。合成了水溶性荧光 AuNCs(平均尺寸为 2.7nm),然后通过碳二亚胺偶联将其与抗体结合。然后用羟胺封闭修饰后的 AuNCs 的表面,以避免与生物组织发生非特异性相互作用。对来自两名死后人类供体的眼部组织切片(厚 5μm)进行了 MT 1/2 和 MT 3 的免疫测定。然后通过荧光共焦显微镜进行成像研究,并在视网膜中进行 LA-ICP-MS 以测量金信号。每个纳米簇中 >500 个金原子的信号放大使得可以通过 LA-ICP-MS 对抗原(MT 1/2 和 MT 3)进行成像,激光光斑大小小至 4μm。在视网膜中发现的图像模式与使用传统荧光免疫组织化学获得的模式非常吻合,后者被用作既定的参考方法。摘要 与初级特异性抗体结合的金纳米簇 (AuNCs) 用作标记物,用于通过激光烧蚀与电感耦合等离子体质谱 (ICP-MS) 耦合对人眼组织切片中的金属硫蛋白 (MTs) 进行放大生物成像。