Nanobind Hierarchical Silica Lamella for High Molecular Weight DNA Extraction

Information

  • Research Project
  • 9150684
  • ApplicationId
    9150684
  • Core Project Number
    R44GM109618
  • Full Project Number
    5R44GM109618-03
  • Serial Number
    109618
  • FOA Number
    PA-14-071
  • Sub Project Id
  • Project Start Date
    9/25/2015 - 9 years ago
  • Project End Date
    8/31/2017 - 7 years ago
  • Program Officer Name
    WU, MARY ANN
  • Budget Start Date
    9/1/2016 - 8 years ago
  • Budget End Date
    8/31/2017 - 7 years ago
  • Fiscal Year
    2016
  • Support Year
    03
  • Suffix
  • Award Notice Date
    8/2/2016 - 8 years ago
Organizations

Nanobind Hierarchical Silica Lamella for High Molecular Weight DNA Extraction

? DESCRIPTION (provided by applicant): As new genetic analysis methods are developed, rising emphasis is being placed on high quality sample preparation and the ability to obtain large quantities of high molecular weight and high purity DNA. In DNA sequencing, 3rd generation technologies offer long read lengths up to 30 kb and require high quality isolated DNA. In gene therapy and DNA vaccines, high binding capacity could be extremely useful in isolating industrial quantities of long plasmids. In genetic analysis of extremely rare sequences or functional analysis of large chromosomal rearrangements, high molecular weight input DNA reduces the chance that fragmentation will occur in a region of interest. In Phase I, we created a novel thermoplastic, silica substrate, containing a hierarchical layering of microscale folds and nanoscale silica lamella called Nanobind. Through the combined effects of minimized shear force exposure and high surface area, we are able to extract vast amounts (10- 100X more) of high molecular weight genomic DNA (>100 kb) using a simple bind, wash, and elute protocol that is both fast (<45 min) and inexpensive ($0.01 per substrate). In this Phase II SBIR, we will develop Nanobind technologies to address 3 areas where critical limitations exist with current extraction methods. First, we will create a facile method for high MW extraction by developing a magnetic Nanobind substrate. Second, current automated extraction systems rely exclusively on beads and columns and tend to fragment DNA to <50 kb. We will develop MagNanobind HTP, a 96-well format for high-throughput, high MW DNA extraction that is compatible with a variety of existing automated extraction instruments. Third, we will develop a microvolume Nanobind cartridge to perform small volume extractions using clinical samples <1 µL or <10 ng. Finally, we will validate the Nanobind DNA/RNA extraction platform by comparing against microparticle, spin column, and precipitation methods using 3 common genetic and epigenetic assays. Nanobind could immediately impact the DNA extraction market as it uniquely combines the speed and ease of microparticles and spin columns with performance of phenol-chloroform.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R44
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    748562
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:748562\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    CIRCULOMICS, INC.
  • Organization Department
  • Organization DUNS
    830377581
  • Organization City
    Baltimore
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    212112840
  • Organization District
    UNITED STATES