Aptamer-Based Nanosensors for Human Health
18th April 2024
Timing : 1 pm EST
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For a list of all talks at the NanoBio seminar Series Spring'24, see here
Advancing our understanding of brain (dys)function necessitates novel nanotools that can monitor chemical signaling in complex biological systems. While advanced methods to record electrical signaling in the brain are prevalent, tools to monitor chemical signaling have been limited. Biosensing of small molecules is particularly challenging in the brain microenvironment due to the need to detect trace concentrations of molecules with limited mass and charge in the presence of nonspecific binding of interfering molecules. Further, neurotransmitters co- exist in different brain regions with structurally similar metabolites. At the Laboratory of Chemical Nanotechnology (CHEMINA), we tackle this challenge by integrating DNA-based recognition elements termed aptamers into nanoscale biosensing platforms. Aptamers are systematically designed oligonucleotide receptors that exhibit highly specific and selective recognition of targets. We employ aptamers designed to recognize small- molecule neurotransmitters such as serotonin and dopamine with high affinity and selectivity. We have developed aptamer-modified nanopipettes with ~10 nm openings that approach the spatial resolution of synapses where neurons communicate (~50 nm). Upon reversible target binding, aptamers undergo a rearrangement of the negatively charged backbone, and these dynamic structural changes can be transduced as measurable changes in current through the nanopore. Nanoscale confinement of the sensor surface results in high sensitivity while simultaneously reducing biofouling for long-term recordings, overcoming a critical bottleneck for clinical biosensors. Extensive experimental and theoretical characterizations of the target-specific aptamer conformational dynamics have led to a fundamental understanding of the mechanisms of our biosensing technologies. Such findings enable generalization of our strategy to monitor hypothetically, any small-molecule analyte of interest.