• DocumentCode
    3303626
  • Title

    Oriented assembly of protein on surfaces

  • Author

    Bachyas, L.G. ; Bhattacharyya, D. ; Anderson, Kimberly W.

  • Author_Institution
    Dept. of Chem., Kentucky Univ., Lexington, KY, USA
  • Volume
    2
  • fYear
    1999
  • fDate
    36434
  • Abstract
    Several approaches that facilitate the oriented assembly of proteins on a variety of surfaces, including membranes, is described. Biotinylation reactions performed under controlled conditions were used to immobilize enzymes in a layer-by-layer fashion onto surfaces modified with avidin or streptavidin. For other enzymes, a specific attachment site was introduced by gene fusion or site-directed mutagenesis. These strategies were applied to achieve site-specific immobilization of several enzymes including alkaline phosphatase, organophosphorus hydrolase, horseradish peroxidase, and subtilisin. The site-specific immobilization led to orientation of the enzyme molecules on the surface of materials and to a higher activity compared to conventional immobilization methods
  • Keywords
    biochemistry; biological techniques; biomembranes; molecular biophysics; proteins; surface chemistry; alkaline phosphatase; avidin; biotinylation reactions; enzyme molecules; enzymes immobilization; gene fusion; horseradish peroxidase; material surface; organophosphorus hydrolase; oriented proteins assembly; site-directed mutagenesis; site-specific immobilization; specific attachment site; streptavidin; subtilisin; Amino acids; Assembly; Biochemistry; Biological materials; Biomembranes; Bioreactors; Chemical engineering; Chemistry; DNA; Protein engineering;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    [Engineering in Medicine and Biology, 1999. 21st Annual Conference and the 1999 Annual Fall Meetring of the Biomedical Engineering Society] BMES/EMBS Conference, 1999. Proceedings of the First Joint
  • Conference_Location
    Atlanta, GA
  • ISSN
    1094-687X
  • Print_ISBN
    0-7803-5674-8
  • Type

    conf

  • DOI
    10.1109/IEMBS.1999.803894
  • Filename
    803894