4.2 Article

The RABiT: high-throughput technology for assessing global DSB repair

Journal

RADIATION AND ENVIRONMENTAL BIOPHYSICS
Volume 53, Issue 2, Pages 265-272

Publisher

SPRINGER
DOI: 10.1007/s00411-014-0514-0

Keywords

Ionizing radiation; DNA repair kinetics; Human lymphocytes; High throughput; Radiation sensitivity

Funding

  1. National Institute of Allergy and Infectious Diseases [U19-AI067773, 1R21-ES019494]
  2. National Institute of Environmental Health Sciences
  3. National Institutes of Health

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At the Center for High-Throughput Minimally Invasive Radiation Biodosimetry, we have developed a rapid automated biodosimetry tool (RABiT); this is a completely automated, ultra-high-throughput robotically based biodosimetry workstation designed for use following a large-scale radiological event, to perform radiation biodosimetry measurements based on a fingerstick blood sample. High throughput is achieved through purpose built robotics, sample handling in filter-bottomed multi-well plates and innovations in high-speed imaging and analysis. Currently, we are adapting the RABiT technologies for use in laboratory settings, for applications in epidemiological and clinical studies. Our overall goal is to extend the RABiT system to directly measure the kinetics of DNA repair proteins. The design of the kinetic/time-dependent studies is based on repeated, automated sampling of lymphocytes from a central reservoir of cells housed in the RABiT incubator as a function of time after the irradiation challenge. In the present study, we have characterized the DNA repair kinetics of the following repair proteins: gamma-H2AX, 53-BP1, ATM kinase, MDC1 at multiple times (0.5, 2, 4, 7 and 24 h) after irradiation with 4 Gy gamma rays. In order to provide a consistent dose exposure at time zero, we have developed an automated capillary irradiator to introduce DNA DSBs into fingerstick-size blood samples within the RABiT. To demonstrate the scalability of the laboratory-based RABiT system, we have initiated a population study using gamma-H2AX as a biomarker.

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