• DocumentCode
    2403774
  • Title

    Protein a for human IgG oriented immobilization on silicon surface for an imaging ellipsometry biosensor

  • Author

    Meng, Yanli ; Chen, Bo

  • Author_Institution
    Changchun Inst. of Opt., Fine Mech. & Phys., Changchun, China
  • fYear
    2009
  • fDate
    3-6 Sept. 2009
  • Firstpage
    1497
  • Lastpage
    1500
  • Abstract
    Imaging ellipsometry biosensor was developed on the basement of imaging ellipsometry for thin-film and surface characterization. Using protein A to immobilize Human IgG on silicon surface for the imaging ellipsometry biosensor immunoassay was studied. As a result, The Human IgG immobilized on silicon surface by protein A bound much more polyclonal antibody than that on hydrophobic surface directly, which indicated that protein A could be used to immobilize Human IgG molecules in a highly oriented manner and Human IgG molecule could maintain its native configuration well on the silicon surface. Furthermore, the absorption quantity of protein A affecting on interaction of human IgG and antibody molecules was investigated. The surface concentration of Human IgG and antibody molecules was enhanced as well as the increasing of the absorption quantity of protein A, but there are no obvious increase when the ratio of surface concentration of protein A layer to that of saturated adsorption is larger than 80%. However, even decrease slightly.
  • Keywords
    adsorption; biosensors; ellipsometry; molecular biophysics; proteins; silicon; Si; absorption; human IgG oriented immobilization; imaging ellipsometry biosensor; polyclonal antibody; protein A; Biosensing Techniques; Humans; Immunoglobulin G; Silicon; Surface Properties;
  • 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.2009.5334162
  • Filename
    5334162