Nanoscale bioelectronic devices
Aberrant activity of electroactive cells underly neurological disorders like epilepsy. Control of ionic current through cell membrane can restore balance to electrochemical signals, but are limited to invasive surgically-implanted devices. To achieve both minimally-invasive and cell-type-specific control, we have developed nanoscale devices for remote control of cellular function. For example, we have demonstrated that remote heating of magnetic nanoparticles was sufficient to activate neurons expressing heat-sensitive ion channels in mice—enabling the first example of minimally-invasive cell type specific control in the deep brain. We are interested in engineering nanoscale devices as actuators and sensors to interface with the nervous system in order to explore the limits of device miniaturization.
Cell-type-specific, non-invasive control of the central and peripheral nervous system would greatly enhance our understanding of neurophysiology. We have demonstrated that the potent channelrhodopsin ChRmine can achieve transcranial photoactivation of defined neural circuits, including midbrain and brainstem structures, at depths of up to 7 mm with millisecond precision. By using systemic viral delivery of ChRmine, we were able to modulate behavior without surgery, enabling implant-free deep brain optogenetics.
Hydrogel tissue chemistry
Imaging biomolecules and cells within their spatial context can provide insight into the function and dysfunction of complex biological systems. Over the past decade, chemical methods to transmute tissue into optically transparent substrates have enabled the mapping of features across multiple length scales (from individual mRNA strands to neural projections spanning the mouse brain) . We have previously identified a number of multifunctional epoxides (commonly used chemical resins used in building and construction) that can stabilize biomolecules and tissue within transparent tissue. This method, called SHIELD, can be used for volumetric mapping of biomolecular features (mRNA, proteins, fluorescent reporters) within intact, fixed tissue.