A simple, sensitive and selective quantum-dot-based western blot method for the simultaneous detection of multiple targets from cell lysates

被引:13
作者
Gilroy, Kathryn L. [1 ]
Cumming, Sarah A. [1 ]
Pitt, Andrew R. [1 ]
机构
[1] Univ Glasgow, Fac Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Quantum dot; Protein A/G; Multiplexing; Western blot; PROTEIN MICROARRAYS; NANOPARTICLES; ANTIBODIES;
D O I
10.1007/s00216-010-3908-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantum dots (Qdots) are fluorescent nanoparticles that have great potential as detection agents in biological applications. Their optical properties, including photostability and narrow, symmetrical emission bands with large Stokes shifts, and the potential for multiplexing of many different colours, give them significant advantages over traditionally used fluorescent dyes. Here, we report the straightforward generation of stable, covalent quantum dot-protein A/G bioconjugates that will be able to bind to almost any IgG antibody, and therefore can be used in many applications. An additional advantage is that the requirement for a secondary antibody is removed, simplifying experimental design. To demonstrate their use, we show their application in multiplexed western blotting. The sensitivity of Qdot conjugates is found to be superior to fluorescent dyes, and comparable to, or potentially better than, enhanced chemiluminescence. We show a true biological validation using a four-colour multiplexed western blot against a complex cell lysate background, and have significantly improved previously reported nonspecific binding of the Qdots to cellular proteins.
引用
收藏
页码:547 / 554
页数:8
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