BRAIN EAGER: Genetically Encoded Light Sources for Non-Invasive Optogenetics

Information

  • NSF Award
  • 1464686
Owner
  • Award Id
    1464686
  • Award Effective Date
    10/1/2014 - 10 years ago
  • Award Expiration Date
    8/31/2017 - 7 years ago
  • Award Amount
    $ 300,000.00
  • Award Instrument
    Standard Grant

BRAIN EAGER: Genetically Encoded Light Sources for Non-Invasive Optogenetics

PI: Hochgeschwender, Ute H.<br/>Proposal: 1450216<br/>Title: BRAIN EAGER: Genetically Encoded Light Sources for Non-Invasive Optogenetics<br/><br/>Significance<br/>The realization of light-driven genetically targeted neuronal activation and silencing has led to unprecedented possibilities in manipulating neuronal activity in the behaving experimental animal.<br/>However, translation of this approach into the clinical arena for potential therapeutic applications is complicated by the need for implanting optical fibers in the brain as the light source for activating lightsensing opsins. This proposal describes an integrated research, education, and outreach program which focuses on developing a new generation of genetically encoded light sources for non-invasive manipulation of optogenetic sensors. If successful this will be a key threshold advance that will provide the foundation for new technologies enabling minimally invasive and highly efficient diagnostics and therapies. Currently there are no alternative approaches which would achieve, non-invasively, the full range of photonic control of neurons as proposed here.<br/><br/>Technical Description<br/>The investigators will build on the highly innovative concept of combining optogenetics with bioluminescence. To exploit the concept?s potential for non-invasive light activation of optogenetic sensors in clinical settings, they will utilize protein engineering to both improve light output and extend the emission spectrum of the luciferase by optimizing intramolecular bioluminescence resonance energy transfer (BRET) between Gaussia luciferase and various fluorescent proteins. They will test the novel constructs for their efficiency in activating channelrhodopsins and proton and chloride pumps in vitro. The development of these concepts and reagents will have potentially transformative and broad impacts on the implementations of optogenetics in medicine.

  • Program Officer
    Leon Esterowitz
  • Min Amd Letter Date
    1/20/2015 - 10 years ago
  • Max Amd Letter Date
    1/20/2015 - 10 years ago
  • ARRA Amount

Institutions

  • Name
    Central Michigan University
  • City
    Mount Pleasant
  • State
    MI
  • Country
    United States
  • Address
    Office of Research & Graduate St
  • Postal Code
    488590001
  • Phone Number
    9897746777

Investigators

  • First Name
    Ute
  • Last Name
    Hochgeschwender
  • Email Address
    ute.hochgeschwender@cmich.edu
  • Start Date
    1/20/2015 12:00:00 AM

Program Element

  • Text
    BIOPHOTONICS, IMAGING &SENSING
  • Code
    7236
  • Text
    EFRI RESEARCH PROJECTS
  • Code
    7633

Program Reference

  • Text
    Neuro-photonics
  • Text
    EAGER
  • Code
    7916
  • Text
    Understanding the Brain/Cognitive Scienc
  • Code
    8089
  • Text
    BRAIN Initiative Res Support
  • Code
    8091