4.8 Article

A label-free electrical impedimetric biosensor for the specific detection of Alzheimer's amyloid-beta oligomers

Journal

BIOSENSORS & BIOELECTRONICS
Volume 56, Issue -, Pages 83-90

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2013.12.036

Keywords

Alzheimer's; Amyloid-beta; Biosensor; Prion; Impedance

Funding

  1. Alzheimer's Research UK [PG2010-2]
  2. Fully-Funded International Research Scholarship (FIRS, University of Leeds)
  3. Alzheimers Research UK [ARUK-PG2013-12, ART-PG2010-2] Funding Source: researchfish
  4. MRC [MR/L023784/1] Funding Source: UKRI

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Alzheimer's disease (AD) is the most common form of dementia, with over 37 million sufferers worldwide and a global cost of over $600 billion. There is currently no cure for AD and no reliable method of diagnosis other than post-mortem brain examination. The development of a point-of-care test for AD is an urgent requirement in order to provide earlier diagnosis and, thus, useful therapeutic intervention. Here, we present a novel, label-free impedimetric biosensor for the specific detection of amyloid-beta oligomers (A beta O), which are the primary neurotoxic species in AD. A beta O have been proposed as the best biomarker for AD and levels of A beta O in the blood have been found to correlate with cerebrospinal fluid load. The biorecognition element of our biosensor is a fragment of the cellular prion protein (PrPc, residues 95-110), a highly expressed synaptic protein which mediates the neuronal binding and toxicity of A beta O. During the layer-by-layer sensor construction, biotinylated PrPc (95-110) was attached via a biotin/NeutrAvidin bridge to polymer-functionalised gold screen-printed electrodes. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry and scanning electron microscopy were used to validate biosensor assembly and functionality. EIS was employed for biosensor interrogation in the presence of A beta oligomers or monomers. The biosensor was specific for the detection of synthetic A beta O and gave a linear response, without significant detection of monomeric A beta, down to an equivalent A beta O concentration of similar to 0.5 pM. The biosensor was also able to detect natural, cell-derived A beta O present in conditioned medium. The eventual commercialisation of this biosensor system could allow for the early diagnosis and disease monitoring of AD. (C) 2013 Elsevier B.V. All rights reserved.

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