The use of graphene-based field-effect transistors in the past decade has been shown as one of the most powerful biosensing units for the detection of numerous biological and biochemical analytes.
Distinctly specific electrical properties of graphene in the domain of field-effect transistors, along with high surface-to-volume ratio contribute to incredibly high sensitivity of this type of biosensor, which allows the development of reliable and fast point-of-care (POC) devices for the detection of different types of analytes in real time.
To ensure the selectivity of such biosensors, the graphene channel in transistors is functionalized with the variety of biorecognition elements, such as enzymes, antibodies, and aptamers.
Aptamers are synthetic oligonucleotides developed in purpose of highly specific binding to the target molecule in the same manner as antibodies. The precedence of aptamers lies in their scalability and low-cost production, yet similar binding properties to antibodies, which enables technological benefits of graphene-based aptasensor development.
The principle of detection of target molecules via aptamers relies on aptamer 3D reconfiguration during binding, leading to electric charge redistribution in the vicinity of the graphene surface and latter change of its electrical characteristics.
In view of the ‘liquid-gated’ regime of these biosensors, where the field effect is manifested by ionic charge redistribution in electrolyte, the impact of such redistribution can have considerable impact on biosensor performance, primarily on aptamer 3D reconfiguration.
Currently, graphene-based aptasensors have found its application in the detection of large molecules, e.g., proteins, where the main impact on graphene properties is given by the analyte. On the other hand, the development of graphene-based aptasensors for the detection of small molecules, e.g., toxins, is still challenging for researchers.
A group of researchers from BioSense Institute (Serbia), University of Texas at Austin (USA), National Research University of Electronic Technology (Russia), and A.K. Prokhorov General Physics Institute of the Russian Academy of Sciences (Russia), have proposed a microscopic model of mycotoxin detection via graphene-based aptasensors enabling improvement of biosensor sensitivity, which is based on the investigation of aptamer interaction mechanism with graphene channel during binding of targeted molecules (Biosensors & Bioelectronics.
Namely, it has been shown how aptamers interact with a graphene surface after their anchoring via linker molecules in terms of mycotoxin detection. The model proposes aptamer adsorption on the graphene surface via π-π interaction achieving a significant modulation of charge carriers in graphene crystal lattice due to negatively charged aptamer backbone.
During binding of specific molecules, aptamers change their configuration and drawing away the chargers from graphene surface, which is manifested by graphene electrical properties change. In other words, different charge distribution in the vicinity of graphene surface leads to the desired signal of the biosensor.
To validate their model, the researchers used electrolyte solutions with different ionic strengths (i.e., ion concentration) to modulate capacitive ability of the electrolyte during gating effect.Découvrez aussi
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