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用于细胞和临床肿瘤组织中表皮生长因子受体免疫荧光标记的锰掺杂硫化锌纳米晶体

Mn-doped zinc sulphide nanocrystals for immunofluorescent labeling of epidermal growth factor receptors on cells and clinical tumor tissues.

作者信息

Aswathy J, Seethalekshmy N V, Hiran K R, Bindhu M R, Manzoor K, Nair Shantikumar V, Menon Deepthy

机构信息

Amrita Center for Nanosciences and Molecular Medicine, Amrita Vishwa Vidyapeetham University, Cochin, 682 041 Kerala, India.

出版信息

Nanotechnology. 2014 Nov 7;25(44):445102. doi: 10.1088/0957-4484/25/44/445102. Epub 2014 Oct 10.

Abstract

The field of molecular detection and targeted imaging has evolved considerably with the introduction of fluorescent semiconductor nanocrystals. Manganese-doped zinc sulphide nanocrystals (ZnS:Mn NCs), which are widely used in electroluminescent displays, have been explored for the first time for direct immunofluorescent (IF) labeling of clinical tumor tissues. ZnS:Mn NCs developed through a facile wet chemistry route were capped using amino acid cysteine, conjugated to streptavidin and thereafter coupled to biotinylated epidermal growth factor receptor (EGFR) antibody utilizing the streptavidin-biotin linkage. The overall conjugation yielded stable EGFR antibody conjugated ZnS:Mn NCs (EGFR ZnS:Mn NCs) with a hydrodynamic diameter of 65 ± 15 nm, and having an intense orange-red fluorescence emission at 598 nm. Specific labeling of EGF receptors on EGFR(+ve) A431 cells in a co-culture with EGFR(-ve) NIH3T3 cells was demonstrated using these nanoprobes. The primary antibody conjugated fluorescent NCs could also clearly delineate EGFR over-expressing cells on clinical tumor tissues processed by formalin fixation as well as cryopreservation with a specificity of 86% and accuracy of 88%, in comparison to immunohistochemistry. Tumor tissues labeled with EGFR ZnS:Mn NCs showed good fluorescence emission when imaged after storage even at 15 months. Thus, ZnS nanobioconjugates with dopant-dependent and stable fluorescence emission show promise as an efficient, target-specific fluorophore that would enable long term IF labeling of any antigen of interest on clinical tissues.

摘要

随着荧光半导体纳米晶体的引入,分子检测和靶向成像领域有了显著发展。广泛应用于电致发光显示器的锰掺杂硫化锌纳米晶体(ZnS:Mn NCs)首次被用于临床肿瘤组织的直接免疫荧光(IF)标记。通过简便的湿化学路线制备的ZnS:Mn NCs用氨基酸半胱氨酸进行封端,与链霉亲和素偶联,然后利用链霉亲和素 - 生物素连接与生物素化的表皮生长因子受体(EGFR)抗体偶联。整体偶联产生了稳定的EGFR抗体偶联的ZnS:Mn NCs(EGFR ZnS:Mn NCs),其流体动力学直径为65±15 nm,在598 nm处有强烈的橙红色荧光发射。使用这些纳米探针证明了在与EGFR(-ve)NIH3T3细胞共培养的EGFR(+ve)A431细胞上EGF受体的特异性标记。与免疫组织化学相比,与一抗偶联的荧光纳米晶体也能清晰地勾勒出经福尔马林固定以及冷冻保存处理的临床肿瘤组织上EGFR过表达细胞,特异性为86%,准确率为88%。用EGFR ZnS:Mn NCs标记的肿瘤组织即使在储存15个月后成像时仍显示出良好的荧光发射。因此,具有掺杂剂依赖性和稳定荧光发射的ZnS纳米生物共轭物有望成为一种高效、靶向特异性的荧光团,能够对临床组织上任何感兴趣的抗原进行长期IF标记。

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