Small, high-affinity ligands for array tomography

Information

  • Research Project
  • 9140747
  • ApplicationId
    9140747
  • Core Project Number
    R41MH110321
  • Full Project Number
    1R41MH110321-01
  • Serial Number
    110321
  • FOA Number
    PA-15-270
  • Sub Project Id
  • Project Start Date
    7/1/2016 - 10 years ago
  • Project End Date
    6/30/2017 - 9 years ago
  • Program Officer Name
    GRABB, MARGARET C.
  • Budget Start Date
    7/1/2016 - 10 years ago
  • Budget End Date
    6/30/2017 - 9 years ago
  • Fiscal Year
    2016
  • Support Year
    01
  • Suffix
  • Award Notice Date
    6/30/2016 - 10 years ago
Organizations

Small, high-affinity ligands for array tomography

? DESCRIPTION (provided by applicant): Neurodegenerative diseases are among the most expensive, disruptive, and least well treated of human maladies, arguably because they are not well understood. Array tomography (AT) is a method for tissue imaging with resolution in all three dimensions sufficient to resolve individual synapses and provide quantitative characterization of multiple molecular constituents. AT imaging data enable description of neural networks in the context of the three-­?dimensional tissue architecture. We beleve such data will enable researchers to begin to comprehend the proper function of neural circuits and, importantly, to begin to understand how it is that the various neurodegenerative processes present and progress. AT is, however, complex and expensive, and has been used in relatively few studies following the first publication in 2007 by Micheva and Smith. Aratome is currently providing AT services to the research community. The present application proposes proof-­?of-­?concept studies that a novel ligand development approach can be used to make ligands for AT that are superior to primary antibodies, in that 1) they can be bacterially expressed, which would make the reagents relatively inexpensive and of uniform quality; and 2) they are very small (45 amino acis) so that they will likely have greater access to target binding motifs, which is a major problem with the resin-­?embedded tissue used for AT. Assuming we obtain proof-­?of-­ concept under the present Phase 1 proposal, we would develop a catalog of reagents in Phase 2, which would be made generally available, and which would be integrated into a fully automated AT system, analogous to a NextGen Sequencer, that we are developing using separate funding.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    R41
  • Administering IC
    MH
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    225000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    242
  • Ed Inst. Type
  • Funding ICs
    NIMH:225000\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ARATOME, LLC
  • Organization Department
  • Organization DUNS
    967959730
  • Organization City
    MENLO PARK
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    940251449
  • Organization District
    UNITED STATES