Technology ID
TAB-2899

Highly Sensitive Tethered-Bead Immune Sandwich Assay

E-Numbers
E-188-2014-0
Lead Inventor
Silver, Jonathan (NHLBI)
Co-Inventors
Neuman, Keir (NHLBI)
Li, Zhenyu (George Washington University)
Applications
Therapeutics
Research Materials
Diagnostics
Consumer Products
Therapeutic Areas
Oncology
Infectious Disease
Immunology
Cardiology
Development Stages
Discovery
Development Status
  • Early-stage
  • Prototype
Research Products
Research Equipment
Antibodies
Lead IC
NHLBI
ICs
NHLBI
This technology is a highly sensitive tethered-bead immune sandwich assay. Analyte molecules are captured between two antibodies, a capture antibody and a detection antibody. The capture antibody on a micron-size bead binds analyte from a sample fluid. The bead-captured analyte is then exposed to a “detection” antibody that binds to the bead-captured analyte, forming a “sandwich”. The sandwiched analyte-bead complex then connects to a flexible polymer (such as DNA) anchored on a solid surface to form tethered particles. Binding the analyte-bead complex to a flexible polymer forms tethered particles and may be done, for example, by streptavidin biotin. Motion of the tethered beads easily identifies bound analyte. The tethered beads are quantified using low-magnification light microscopy. Prior enhanced sensitivity tethered bead technologies require expensive and cumbersome detection equipment. This assay is inherently single molecule, low background, and works with simple inexpensive imaging formats, but is automatable and potentially adaptable to portable technologies. A prototype design using prostate specific antigen (PSA) shows detection sensitivity of ~.03ng/ml, compared with normal PSA sensitivity of ~ 4ng/ml. Design refinements further improve sensitivities.
Commercial Applications
  • Diagnostics and research.
Competitive Advantages
  • Highly sensitive single molecule adaptable format, specific, low background, inexpensive, simple to use, automatable for image analysis.
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