Publications by authors named "Sun-Heui Yoon"

Advancements in neural interface technologies have enabled the direct connection of neurons and electronics, facilitating chemical communication between neural systems and external devices. One promising approach is a synaptogenesis-involving method, which offers an opportunity for synaptic signaling between these systems. Janus synapses, one type of synaptic interface utilizing synaptic cell adhesion molecules for interface construction, possess unique features that enable the determination of location, direction of signal flow, and types of neurotransmitters involved, promoting directional and multifaceted communication.

View Article and Find Full Text PDF
Article Synopsis
  • - Seamless neural interfaces that combine neurons with electrochemical devices can enhance communication between neural systems and the outside world by using the same chemical signals that neurons naturally communicate with.
  • - New strategies like synaptic interfaces, iontronics for neuromodulation, and advanced neurosensing techniques are being developed to create efficient connections for neuro-electronic communication.
  • - This perspective highlights ongoing innovations to improve the interaction between neurons and electrodes, focusing on targeting specific parts of neurons, such as synapses, while also discussing advancements in electrochemical sensing and chemical delivery through iontronics.
View Article and Find Full Text PDF

Coordination of synapses onto electrodes with high specificity and maintaining a stable and long-lasting interface have importance in the field of neural interfaces. One potential approach is to present ligands on the surface of electrodes that would be bound through a protein-protein interaction to specific areas of neuronal cells. Here, we functionalize electrode surfaces with genetically engineered neuroligin-1 protein and demonstrate the formation of a nascent presynaptic bouton upon binding to neurexin-1 β on the presynaptic membrane of neurons.

View Article and Find Full Text PDF

Over the recent years, the development of neural interface systems has stuck to using electrical cues to stimulate neurons and read out neural signals, although neurons relay signals via chemical release and recognition at synapses. In addition, conventional neural interfaces are vulnerable to cell migration and glial encapsulation due to the absence of connection anchoring the neuron into the device unlike synapses, which are firmly sustained by protein bonding. To close this discrepancy, we conducted an intensive investigation into the induced synapse interface by employing engineered synaptic proteins from a neural interface perspective.

View Article and Find Full Text PDF

A novel pump-free miniaturized reverse electrodialysis (RED) system was designed to provide lasting power transduced from salinity gradients, named solid salt RED (ssRED), and this quasi-battery uses a solid salt instead of electrolyte solution for streamlined usage. It is portable, flexible, comparable in size to a universal serial bus flash drive, and easily activated with a small amount of water. It maintains a constant ionic concentration gradient through precipitation reactions between a pair of different salts.

View Article and Find Full Text PDF

We suggest an electrochemiluminescence (ECL)-sensing platform driven by ecofriendly, disposable, and miniaturized reverse electrodialysis (RED) patches as an electric power source. The flexible RED patches composed of ion-exchange membranes (IEMs) can produce voltage required for ECL sensing by simply choosing the appropriate number of IEMs and the ratio of salt concentrations. We integrate the RED patch with a bipolar electrode on the microfluidic chip to demonstrate the proof-of-concept, i.

View Article and Find Full Text PDF
Article Synopsis
  • - Cas9-linked deaminases, known as base editors, allow precise modification of single nucleotides in eukaryotic DNA, but their potential off-target effects are still not fully understood.
  • - The study modifies a method called Digenome-seq to evaluate the specificity of a specific base editor combining nCas9 and the deaminase APOBEC1 in human DNA.
  • - Results show that the rAPOBEC1-nCas9 base editor is quite accurate, causing only 18 ± 9 unintended changes per single guide RNA in the genome, with off-target effects differing from traditional Cas9 editing.
View Article and Find Full Text PDF
Article Synopsis
  • - The study investigates CRISPR Cpf1 endonucleases, which are enzymes that use single RNA guides to create specific double-stranded breaks in DNA, focusing on their targeting specificity compared to the widely used CRISPR-Cas9.
  • - Researchers found that Cpf1 can handle mismatches in certain regions of the RNA guide, specifically tolerating them better in the 3' region compared to the 5' region.
  • - A genome-wide analysis showed that Cpf1 has significantly fewer cleavage sites in the human genome than Cas9, and most off-target cuts by Cpf1 do not result in mutations when tested in cells, with the possibility of eliminating off-target effects through specific protein-RNA complexes
View Article and Find Full Text PDF