• 文献标题:   Graphene oxide based fluorescent aptasensor for adenosine deaminase detection using adenosine as the substrate
  • 文献类型:   Article
  • 作  者:   XING XJ, LIU XG, YUEHE, LUO QY, TANG HW, PANG DW
  • 作者关键词:   graphene oxide, aptamer, adenosine, adenosine deaminase, inhibition
  • 出版物名称:   BIOSENSORS BIOELECTRONICS
  • ISSN:   0956-5663
  • 通讯作者地址:   Wuhan Univ
  • 被引频次:   46
  • DOI:   10.1016/j.bios.2012.04.037
  • 出版年:   2012

▎ 摘  要

We present a novel fluorescent aptasensor for simple and accurate detection of adenosine deaminase (ADA) activity and inhibition on the basis of graphene oxide (GO) using adenosine (AD) as the substrate. This aptasensor consists of a dye-labeled single-stranded AD specific aptamer, GO and AD. The fluorescence intensity of the dye-labeled AD specific aptamer is quenched very efficiently by GO as a result of strong pi-pi stacking interaction and excellent electronic transference of GO. In the presence of AD, the fluorescence of the GO-based probe is recovered since the competitive binding of AD and GO with the dye-labeled aptamer prevents the adsorption of dye-labeled aptamer on GO. When ADA was introduced to this GO-based probe solution, the fluorescence of the probe was quenched owing to ADA cm convert AD into inosine which has no affinity to the dye-labeled aptamer, thus allowing quantitative investigation of ADA activity. The as-proposed sensor is highly selective and sensitive for the assay of ADA activity with a detection limit of 0.0129 U/mL in clean buffer, which is more than one order of magnitude lower than the previous reports. Meanwhile, a good linear relationship with the correlation coefficient of R=0.9922 was obtained by testing 5% human serum containing a series of concentrations of ADA. Additionally, the inhibition effect of erythro-9-(2-hydroxy-3-nonyl) adenine on ADA activity was investigated in this design. The GO-based fluorescence aptasensor not only provides a simple, cost-effective and sensitive platform for the detection of ADA and its inhibitor but also shows great potential in the diagnosis of ADA-relevant diseases and drug development. (C) 2012 Elsevier B.V. All rights reserved.