• DocumentCode
    2091214
  • Title

    Studies on Kinetics of Reaction Between Peroxynitrite and Tryptophan

  • Author

    Zhang, Wei ; Luo, Yunjing ; Zhen, Yan ; Wei, Peng ; Zhong, Rugang

  • Author_Institution
    Beijing Univ. of Technol., Beijing
  • fYear
    2007
  • fDate
    23-27 May 2007
  • Firstpage
    1602
  • Lastpage
    1605
  • Abstract
    Peroxynitrite (ONOO-) is a potent cytotoxin, and it can damage tryptophan, tyrosine and other biomolecules. The kinetics of tryptophan damaged by peroxynitrite was studied by stopped-flow spectrophotometer at 25degC. When peroxynitrite is present in excess, there are many products formed including nitrotryptophan, hydroxytryptohan, N-formylkinurenine or dihydroxytryptophan, oxindole, and hydropyrroloindole. The kinetics of tryptophan loss can represent the kinetics of peroxynitrite damaging tryptophan as a whole. The kinetics of this reaction was studied by monitoring the decrease of fluorescence of tryptophan, and the apparrent second order rate, 2.85 x 104 Mmiddot1 smiddot1, and the apparent activation energy, 39.4 kJ-molmiddot1 are derived.
  • Keywords
    biochemistry; biomedical measurement; cellular biophysics; chemical variables measurement; fluorescence; neurophysiology; organic compounds; reaction kinetics; spectrochemical analysis; spectrophotometry; toxicology; N-formylkinurenine; apparent activation energy; biomolecules; cytotoxin; dihydroxytryptophan; fluorescence monitoring; hydropyrroloindole; hydroxytryptohan formation; nitrotryptophan formation; oxindole; peroxynitrite; reaction kinetics; stopped-flow spectrophotometer; temperature 25 C; tryptophan damage; tyrosine; Amino acids; Biomedical engineering; Biomedical monitoring; Chemicals; Condition monitoring; Educational institutions; Fluorescence; Kinetic theory; Molecular biophysics; Power engineering and energy;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-1077-4
  • Electronic_ISBN
    978-1-4244-1078-1
  • Type

    conf

  • DOI
    10.1109/ICCME.2007.4382017
  • Filename
    4382017