SBIR/STTR Research Award

Enabling technologies for rapid and low cost molecular diagnosticshttps://apps.era.nih.gov/grantfolder/grantfolder/viewGrantFolder.do?businessAreaCode=GM&applID=8930749&folderID=90

Award identifier 83f6d9c5048bb3822f630570591dfbe315a0e510c1e16406d6c435a37afd6059Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$657,899

Program and phase

SBIR · Phase I

Award year

2014

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Atharva LLC (dba Atharva Sciences)
Proposal award date
2014-09-22
Contract end date
2016-08-31
UEI
Not reported
Solicitation number
PA11-134
Topic code
172

Research abstract

DESCRIPTION provided by applicant Molecular techniques including diagnostics that require separation or identification of different sized nucleic acid sequences have remained unchanged over the last several decades and rely primarily on some form of electrophoresis Diagnostics for several human diseases such as those associated with trinucleotide repeat instability exemplified by Fragile X syndrome currently require these conventional techniques These conventional techniques have inherent disadvantages of being labor intensive and less amenable to automation and also not suitable for being developed into screening platforms We have been developing a unique technology for DNA separation and fractionation that overcomes many of the limitations of current DNA separation technologies such as electrophoresis The technology is based on first tethering the DNA molecule to a solid surface through precise end hybridization and then sequentially pulling the DNA off the surface under an electric field The anchor is such designed that the critical force to detach a DNA chain is independent of the chain length Because the electrical force is proportional to the DNA net charge a gradual increase of the electric field leads to size based selection of the DNA strands longer DNA molecules depart the surface first followed by the shorter ones Significantly this highly efficient method does not require use of a matrix like agarose or PAGE and has no upper or lower limit on the length of DNA that can be separated This innovative DNA separation method is now being proposed to be developed into an instrument that can serve as a key platform technology primarily for the diagnosis of trinucleotide repeat instability associated genetic diseases diagnostics and screening The device and technology was developed at the University of Pittsburgh but has not yet been available to other researchers beyond the original investigators In this project a commercial development of this novel idea is planned that it will make a significant impact in a wide variety of clinical and research scenarios PUBLIC HEALTH RELEVANCE Molecular techniques including diagnostics that require separation or identification of different sized nucleic acid sequences have remained unchanged over the last several decades and rely primarily on some form of electrophoresis We propose to develop a novel instrument using electric fields to separate long double stranded DNA molecules from shorter ones based on immobilization of DNA molecules on a glass slide through short anchors attached to its surface Significantly this highly efficient method does not depend on a matrix like agarose or PAGE and has no upper or lower limit on the length of DNA that can be separated This innovative DNA separation method is now being proposed to be developed into an instrument that can serve as a key platform technology with a focus on the trinucleotide repeat instability associated genetic diseases diagnostics

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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