| Literature DB >> 31049723 |
Yufang Hu1,2, Qingqing Zhang3, Dandan Hu3, Jiao Wang3, Jiajia Rao3, Lihua Xu3, Zhiyong Guo4, Sui Wang3, Xin Liu5, Shiyun Tang5, Qinpeng Shen6.
Abstract
Protein p300 is a transcriptional co-activator that participates in many physiological processes including cell cycle control, differentiation and apoptosis. It serves (a) as a protein bridge that links specific transcription factors to the fundamental transcription machinery, (b) as a scaffold to complete multiple transcription cofactors, and (c) as an enzyme for acetylating histone and non-histone proteins. An ultrasensitive electrochemiluminescence (ECL) immunosensor is described here that is based on the use of a magnetic glassy carbon electrode modified with tetrahedral DNA with hollow structure, graphene oxide (GO) and gold nanocrystals. The use of a GO monolayer allows for greater carrying capacity and warrants a wider outer Helmholtz plane. Strong and stable ECL signals were achieved due to antigen-antibody interaction by using the ECL probe Ru(phen)32+. This immunosensor has a response that covers the 0.005 to 80 nM p300 concentration range and has a 1 pM detection limit. It was exploited for the determination of p300 in HeLa cell lysate and (spiked) serum. Graphical abstract Schematic presentation of an ultrasensitive Faraday-cage electrochemiluminescence immunosensor toward the transcriptional co-activator p300 analysis is presented based on a graphene oxide monolayer and tetrahedral DNA-mediated signal amplification.Entities:
Keywords: DNA nanotechnology; Faraday-cage electrochemiluminescence assay; Histone acetyltransferase; Multi-functionalized graphene oxide; Outer Helmholtz plane
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Year: 2019 PMID: 31049723 DOI: 10.1007/s00604-019-3435-4
Source DB: PubMed Journal: Mikrochim Acta ISSN: 0026-3672 Impact factor: 5.833