AnteroTag, a Novel Method for Trans-Synaptic Delivery of Active Agents to Map and Modify Anterograde Populations

Information

  • Research Project
  • 10258693
  • ApplicationId
    10258693
  • Core Project Number
    RF1MH126706
  • Full Project Number
    1RF1MH126706-01
  • Serial Number
    126706
  • FOA Number
    RFA-MH-19-136
  • Sub Project Id
  • Project Start Date
    9/13/2021 - 2 years ago
  • Project End Date
    9/12/2024 - 4 months from now
  • Program Officer Name
    KIM, DOUGLAS S
  • Budget Start Date
    9/13/2021 - 2 years ago
  • Budget End Date
    9/12/2024 - 4 months from now
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/9/2021 - 2 years ago

AnteroTag, a Novel Method for Trans-Synaptic Delivery of Active Agents to Map and Modify Anterograde Populations

PROJECT SUMMARY A goal of the BRAIN initiative is to develop and validate novel tools to map and manipulate neural circuits. The definition and control of behaviorally relevant circuits requires both retrograde and anterograde trans-synaptic technologies that perform well in vivo. In this project, we pursue the long-term goal of developing a small protein tag for the anterograde delivery of cargos (an ?AnteroTag?). The novel concept of AnteroTag is to leverage the endogenous biology of neurotransmission to target tagged payloads to synaptic vesicles where they undergo vesicular release, postsynaptic entry, and desired action. Our consortium of investigators proposes to utilize the pontocerebellar circuit as a model pipeline to further refine and rigorously validate AnteroTag. As the axons of basal pontine neurons (mossy fibers) make specific and quantitative synapses upon cerebellar granule cells, the pontocerebellar circuit affords an established and conserved model circuit to determine how iterations of AnteroTag alter its performance. The investigators of the consortium will leverage their respective areas of expertise to quantify the specificity and biocompatibility of AnteroTag, benchmarked against a current state-of- the-art anterograde viral vector HSV-129; these analyses in mice will include microscopy, electrophysiology, and in vivo activity imaging in behaving animals. Once the pipeline determines the most specific and safe version of AnteroTag in the pontocerebellar circuit, we will assay AnteroTag performance when delivered to diverse starter populations of neurons. The broad utility of AnteroTag will then be determined by testing its efficacy to deliver a variety of genetically encoded markers and modifiers, and by testing AnteroTag derivatives for their utility in accessing second-order anterograde populations. With safety, specificity, and utility thus rigorously demonstrated in mice, we will assay the performance of AnteroTag in the pontocerebellar circuit of higher organisms including tree shrews, ferrets, and NHPs. The outcome of this proposal will be the development, validation, and implementation of a novel technology for the trans-synaptic anterograde delivery of biological agents across multiple brain regions and multiple species. Thus, if successful, our project will ultimately aid in the development of targeted cell-type and circuit-specific therapeutics to treat brain disorders.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    RF1
  • Administering IC
    MH
  • Application Type
    1
  • Direct Cost Amount
    1699630
  • Indirect Cost Amount
    605122
  • Total Cost
    2304752
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    242
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIMH:2304752\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZMH1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    MICHIGAN STATE UNIVERSITY
  • Organization Department
    PEDIATRICS
  • Organization DUNS
    193247145
  • Organization City
    EAST LANSING
  • Organization State
    MI
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    488242600
  • Organization District
    UNITED STATES