Dreadd2.0: A Chemogenetic Toolkit

Summary

Principal Investigator: Bryan L Roth
UNC Neuroscience
Title: " Dreadd2.0: An Enhanced Chemogenetic Toolkit"
BRAIN Category: Tools for Cells and Circuits (RFA MH-14-216)

Dr. Roth and colleagues will build second generation technology that uses artificial neurotransmitters and receptors to manipulate brain activity simultaneously across select cells and pathways to understand their functions and potentially treat brain disorders.

Principal Investigator: Bryan L Roth
UNC Neuroscience
Title: ” Dreadd2.0: An Enhanced Chemogenetic Toolkit”
BRAIN Category: Tools for Cells and Circuits (RFA MH-14-216)

Dr. Roth and colleagues will build second generation technology that uses artificial neurotransmitters and receptors to manipulate brain activity simultaneously across select cells and pathways to understand their functions and potentially treat brain disorders.

NIH Webpages

Roth's Lab has pioneered the use of directed molecular evolution to create GPCRs which are suitable for remotely controlling cellular signaling. Using a variety of mouse genetic approaches (e.g. Cre-mediated recombination. they are able to control neuronal firing and non-neuronal signaling in real-time in awake, freely moving animals.Ongoing projects are to use this technology to deconstruct the neuronal requirements for simple and complex behaviors, particularly as they relate to schizophrenia and drug abuse

Roth’s Lab has pioneered the use of directed molecular evolution to create GPCRs which are suitable for remotely controlling cellular signaling. Using a variety of mouse genetic approaches (e.g. Cre-mediated recombination. they are able to control neuronal firing and non-neuronal signaling in real-time in awake, freely moving animals.Ongoing projects are to use this technology to deconstruct the neuronal requirements for simple and complex behaviors, particularly as they relate to schizophrenia and drug abuse

Project Description

The Brain Research through Advancing Innovative Neurotechnologies (BRAIN) Initiative has the ambitious goal of elucidating how neuronal ensembles interactively encode higher brain processes. To accomplish this goal, new and improved methods for both recording and manipulating neuronal activity will be needed. In this application, we focus on technologies for manipulating neuronal activity. The major significance of this application is that we will provide an enhanced chemogenetic toolbox that allows non-invasive, multiplexed spatiotemporal control of neuronal activity in domains ranging from single synapses to ensembles of neurons. To achieve this, we will provide: Chemical actuators with improved pharmacokinetics and pharmacodyamics suited for use with current DREADDs in eukaryotes ranging from Drosophila to primates (Specific Aim #1) Photo-caged CNO and other chemical actuators to provide millisecond-scale control (Specific Aim #1) Novel DREADDs and ‘split-DREADDs’ targeted to distinct neuronal pathways to enable multiplexed interrogation of neuronal circuits (Specific Aims #2 and 3) Chemogenetic platforms with minimized desensitization and down-regulation (Specific Aim #3)

Public Health Relevance Statement

The Brain Research through Advancing Innovative Neurotechnologies (BRAIN) Initiative has the ambitious goal of elucidating how neuronal ensembles interactively encode higher brain processes-ultimately to provide novel approaches for diagnosing and treating neuropsychiatric diseases. To accomplish this goal, new and improved methods for both recording and manipulating neuronal activity will be needed. Here we provide a chemogenetic platform for manipulating neuronal activity which requires no specialized equipment, and is non-invasive. Further this chemogenetic platform affords multiplexed spatiotemporal control of neuronal activity in domains ranging from single synapses to ensembles of neurons. It is likely that this new chemogenetic platform will be used by large numbers of investigators to elucidate circuitry and neuronal signaling pathways responsible for many neuropsychiatric diseases.

NIH Spending Category

Eye Disease and Disorders of Vision; Neurosciences

Project Terms

Adopted; analog; Animals; base; Brain; brain research; cell type; Chemicals; Communities; desensitization; Designer Drugs; Diagnosis; Disease; Down-Regulation; Drosophila genus; Drug Kinetics; Engineering; Equipment; Eukaryota; G-Protein-Coupled Receptors; Generations; Goals; Grant; Graph; improved; innovation; Ion Channel; Ivermectin; Ligands; Longitudinal Studies; Methods; millisecond; neuronal circuitry; Neurons; neuropsychiatry; Neurosciences; neurotechnology; novel; novel strategies; Opsin; optogenetics; Pathway interactions; Pharmacodynamics; Primates; Principal Investigator; Process; programs; Property; public health relevance; Publications; receptor; recombinase; Research Personnel; Signal Pathway; Signal Transduction; spatiotemporal; Synapses; Techniques; Technology; tool; Translating; Viral

Skip to toolbar