Cell-Penetrating Peptide-Adaptors for Intracellular Cargo Delivery

Information

  • Research Project
  • 9813250
  • ApplicationId
    9813250
  • Core Project Number
    R15EB028609
  • Full Project Number
    9R15EB028609-02
  • Serial Number
    028609
  • FOA Number
    PA-18-504
  • Sub Project Id
  • Project Start Date
    8/1/2019 - 5 years ago
  • Project End Date
    7/31/2022 - 2 years ago
  • Program Officer Name
    ERIM, ZEYNEP
  • Budget Start Date
    8/1/2019 - 5 years ago
  • Budget End Date
    7/31/2022 - 2 years ago
  • Fiscal Year
    2019
  • Support Year
    02
  • Suffix
  • Award Notice Date
    5/24/2019 - 5 years ago

Cell-Penetrating Peptide-Adaptors for Intracellular Cargo Delivery

PROJECT SUMMARY Biomolecules that represent important therapeutic leads are often impractical because they cannot reach their targets, most commonly because of failure to cross cell membranes and reach appropriate subcellular destinations. Cell-penetrating peptides (CPPs) hold great promise for overcoming these failures. CPPs are capable of mediating penetration of the plasma membrane by molecules to which they are coupled, allowing delivery of ?cargos? to cell interiors, a potentially transformative platform technology that can enable an array of specific applications. Nevertheless, development of CPP therapeutics has been disappointing because traditional CPP-cargo molecules largely remain trapped in endosomes rather than reach the cytoplasm. The largest technical hurdle to development of CPP therapeutics is failure to escape from endosomes ? our technology solves this problem. Our innovative approach is the use of high affinity but reversible noncovalent coupling to attach cargos to CPPs. Our prototype CPP-adaptor fusion protein, TAT-Calmodulin (TAT-CaM), consists of the cell penetrating moiety from HIV transactivator of transcription and human calmodulin. TAT-CaM binds CaM binding-site (CBS) containing cargos with nM affinity in the presence of calcium but negligibly in its absence. Because mammalian cells typically maintain low resting concentrations of calcium, cargos dissociate from the CPP-adaptor once inside the cell, releasing cargo to the cytoplasm or other subcellular destination. This R15 AREA renewal application describes efforts to elucidate the mechanisms, kinetics and other basic issues of CPP biology and develop methods to use our CPP-adaptors to deliver nucleic acids such as siRNA for research and therapeutic purposes. We will also utilize them to deliver cargo molecules that will demonstrate the broad utility of our system and its advantages over transfection, namely efficiency, speed and tunability. Success in these endeavors will validate that our strategy is an adaptable tool for delivery of a wide array of macromolecules including nucleic acids, potentially enabling the development of a new generation of therapeutics and research tools.

IC Name
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
  • Activity
    R15
  • Administering IC
    EB
  • Application Type
    9
  • Direct Cost Amount
    300000
  • Indirect Cost Amount
    95641
  • Total Cost
    395641
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    286
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIBIB:395641\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    BBM
  • Study Section Name
    Biochemistry and Biophysics of Membranes Study Section
  • Organization Name
    KENNESAW STATE UNIVERSITY
  • Organization Department
    OTHER BASIC SCIENCES
  • Organization DUNS
    627758923
  • Organization City
    KENNESAW
  • Organization State
    GA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    301445591
  • Organization District
    UNITED STATES