INTERACTION OF MELANIN WITH CARBON-CENTERED AND OXYGEN-CENTERED RADICALS FROM METHANOL AND ETHANOL

被引:34
|
作者
DUNFORD, R
LAND, EJ
ROZANOWSKA, M
SARNA, T
TRUSCOTT, TG
机构
[1] UNIV KEELE, DEPT CHEM, KEELE ST5 5BG, STAFFS, ENGLAND
[2] CHRISTIE HOSP NATL HLTH SERV TRUST, PATERSON INST CANC RES, CRC, DEPT BIOPHYS CHEM, MANCHESTER, LANCS, ENGLAND
[3] JAGIELLONIAN UNIV, INST MOLEC BIOL, DEPT BIOPHYS, KRAKOW, POLAND
关键词
MELANIN; DOPA- AND CYSTEINYL DOPA-MELANINS; CARBON- AND OXYGEN-CENTERED RADICALS; LIPID PEROXIDATION; ELECTRON PARAMAGNETIC RESONANCE SPECTROSCOPY; PULSE RADIOLYSIS; FREE RADICALS;
D O I
10.1016/0891-5849(95)00059-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interaction of dopa-melanin (DM) and cysteinyldopa-melanin (CDM) with carbon- and oxygen-centered radicals generated by benzophenone-photosensitized hydrogen abstraction from ethanol, or by pulse radiolysis of aqueous solutions of methanol and ethanol, is reported. Photosensitized formation of carbon-centered radicals and their interaction with melanin was monitored by electron paramagnetic resonance (EPR) spin trapping using DMPO, and via the melanin free radical signal itself. In the pulse radiolysis experiments, the interaction of DM or CDM with hydroxymethyl, hydroxyethyl, and the corresponding methanol peroxyl radical was monitored by recording time-dependent changes of the melanin absorbance at selected wavelengths. The data indicate that both melanins are good scavengers of carbon-centered radicals, with corresponding rate constants in the range of 10(7) to 10(8) M(-1) s(-1). Significantly, compared to DM, CDM is also an exceptionally efficient scavenger of oxygen-centered radicals derived from methanol with corresponding rate constants of 2.7 x 10(4) and 2 x 10(6) M(-1) s(-1) for DM and CDM, respectively. The results are discussed with reference to the potential role of melanin in protecting the integrity of melanosomes by inhibiting peroxidation of lipid components of the organelle membrane.
引用
收藏
页码:735 / 740
页数:6
相关论文
共 50 条
  • [21] The interaction of carbon-centered radicals with copper(I) and copper(II) complexes
    Ribelli, Thomas G.
    Matyjaszewski, Krzysztof
    Poli, Rinaldo
    JOURNAL OF COORDINATION CHEMISTRY, 2018, 71 (11-13) : 1641 - 1668
  • [22] Temperature dependence of initiation reactions of oxygen-centered radicals
    Watanabe, Y
    Ishigaki, H
    Okada, H
    Suyama, S
    POLYMER JOURNAL, 1997, 29 (08) : 693 - 696
  • [23] Substitution of β-nitrostyrenes by electrophilic carbon-centered radicals
    García-Torres, A
    Cruz-Almanza, R
    Miranda, LD
    TETRAHEDRON LETTERS, 2004, 45 (10) : 2085 - 2088
  • [24] Oxygen-Centered Radicals Formed in the Reaction Mixtures Containing Chloroiron Tetraphenylporphyrin, lodosylbenzene, and Ethanol
    Nishizaki, Daisuke
    Iwahashi, Hideo
    INORGANIC CHEMISTRY, 2017, 56 (21) : 13166 - 13173
  • [25] Carbon-centered radicals in isolated soy proteins
    Boatright, W. L.
    Jahan, M. S.
    Walters, B. M.
    Miller, A. F.
    Cui, D.
    Hustedt, E. J.
    Lei, Q.
    JOURNAL OF FOOD SCIENCE, 2008, 73 (03) : C222 - C226
  • [26] Carbon-Centered Radicals in Cigarette Smoke: Acyl and Alkylaminocarbonyl Radicals
    Bartalis, Judit
    Zhao, Yi-Lei
    Flora, Jason W.
    Paine, John B., III
    Wooten, Jan B.
    ANALYTICAL CHEMISTRY, 2009, 81 (02) : 631 - 641
  • [27] Kinetic studies of the rich interaction of cannabinoids with oxygen-centered radicals and excited carbonyl compounds
    Frank, Carly J.
    Joshi, Neeraj
    Durst, Tony
    Scaiano, Juan C.
    FREE RADICAL BIOLOGY AND MEDICINE, 2025, 232 : 194 - 199
  • [28] A platform for blue-luminescent carbon-centered radicals
    Li, Xin
    Wang, Yi-Lin
    Chen, Chan
    Ren, Yan-Yan
    Han, Ying-Feng
    NATURE COMMUNICATIONS, 2022, 13 (01)
  • [29] Redox chemistry of carbon-centered α-amino acid radicals
    Jonsson, M
    Kraatz, HB
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1997, (12): : 2673 - 2676
  • [30] Factors controlling the addition of carbon-centered radicals to alkenes
    Fischer, H
    Radom, L
    MACROMOLECULAR SYMPOSIA, 2002, 182 : 1 - 14