Quantitative multiplexed quantum dot immunohistochemistry

被引:50
作者
Sweeney, E. [2 ]
Ward, T. H. [2 ]
Gray, N. [3 ]
Womack, C. [3 ]
Jayson, G. [2 ]
Hughes, A. [3 ]
Dive, C.
Byers, R. [1 ,4 ]
机构
[1] Univ Manchester, Sch Canc & Imaging Studies, Manchester M13 9PT, Lancs, England
[2] Paterson Inst Canc Res, Translat Angiogenesis Grp, Manchester M20 4BX, Lancs, England
[3] AstraZeneca, Macclesfield SK10 4TC, Cheshire, England
[4] Manchester Royal Infirm, Dept Histopathol, Manchester M13 9WL, Lancs, England
基金
英国医学研究理事会;
关键词
quantum dot; QDot; immunohistochemistry; nanocrystal; spectral imaging;
D O I
10.1016/j.bbrc.2008.06.127
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quantum dots are photostable fluorescent semiconductor nanocrystals possessing wide excitation and bright narrow, symmetrical, emission spectra. These characteristics have engendered considerable interest in their application in Multiplex immunohistochemistry for biomarker quantification and co-localisation in clinical samples. Robust quantitation allows biomarker validation, and there is growing need for Multiplex staining due to limited quantity of clinical samples. Most reported multiplexed quantum dot staining used sequential methods that are laborious and impractical in a high-throughput setting. Problems associated with sequential Multiplex staining have been investigated and a method developed using QDs conjugated to biotinylated primary antibodies, enabling Simultaneous multiplex staining with three antibodies. CD34, Cytokeratin 18 and cleaved Caspase 3 were triplexed in tonsillar tissue using an 8 h Protocol, each localised to separate cellular compartments. This demonstrates utility of the method for biomarker measurement enabling rapid measurement of multiple co-localised biomarkers on single Paraffin tissue sections, of importance for clinical trial studies. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:181 / 186
页数:6
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