• DocumentCode
    2422981
  • Title

    Integrated microfluidic enzyme reactor mass spectrometry platform for detection of anthrax lethal factor

  • Author

    Aravamudhan, Shyam ; Joseph, Paul J. ; Kuklenyik, Zsuzsanna ; Boyer, Anne E. ; Barr, John R.

  • Author_Institution
    Nanotechnol. Res. Center, Georgia Inst. of Technol., Atlanta, GA, USA
  • fYear
    2009
  • fDate
    3-6 Sept. 2009
  • Firstpage
    1071
  • Lastpage
    1074
  • Abstract
    In this work, we have developed a coupled microfluidic enzyme reactor mass spectrometry platform for the detection of protein toxins such as anthrax lethal factor. The lethal toxin produced during Bacillus anthracis infection is a complex protective antigen, which localizes the toxin to the cell receptor and lethal factor (LF). We have demonstrated, in this work, the applicability of a microfluidic reactor for the capture and concentration of enzyme reaction solid-phase. The reaction solid-phase consists of anti-LF monoclonal antibodies immobilized on magnetic protein G beads for the capture of LF. The captured LF, on exposure to optimized peptide substrate, hydrolyzes into two smaller peptide products. These cleavage products were then analyzed by mass spectrometer coupled to the microfluidic reactor. This resulted in efficient sample preparation, high sensitivity, larger reaction sites, less reagents consumption and shorter analysis time. We have showed here reproducible detection of anthrax lethal factor in concentration range of 40 to 0.5 ng/mL with a detection limit of 1 ng/mL. The enzymatic reaction and the analysis were performed in less than 15 minutes, indicating a rapid diagnostic tool for early anthrax prognosis.
  • Keywords
    bioMEMS; biochemistry; biohazards; bioreactors; cellular biophysics; diseases; mass spectroscopic chemical analysis; microfluidics; microorganisms; molecular biophysics; proteins; terrorism; Bacillus anthracis infection; anthrax lethal factor detection; anthrax prognosis; bioterrorism; cell receptor; complex protective antigen; enzyme reaction solid-phase concentration; hydrolysis; integrated microfluidic enzyme reactor mass spectrometry platform; magnetic protein G beads; monoclonal antibody immobilization; protein toxin detection; Antigens, Bacterial; Bacterial Toxins; Endopeptidases; Equipment Design; Equipment Failure Analysis; Immunomagnetic Separation; Mass Spectrometry; Microfluidic Analytical Techniques; Reproducibility of Results; Sensitivity and Specificity; Specimen Handling; Systems Integration;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
  • Conference_Location
    Minneapolis, MN
  • ISSN
    1557-170X
  • Print_ISBN
    978-1-4244-3296-7
  • Electronic_ISBN
    1557-170X
  • Type

    conf

  • DOI
    10.1109/IEMBS.2009.5335064
  • Filename
    5335064