Copper Sources for Sod1 Activation

被引:45
|
作者
Boyd, Stefanie D. [1 ]
Ullrich, Morgan S. [1 ]
Skopp, Amelie [1 ]
Winkler, Duane D. [1 ]
机构
[1] Univ Texas Dallas, Dept Biol Sci, 800 W Campbell Rd, Richardson, TX 75080 USA
基金
美国国家卫生研究院;
关键词
Sod1; copper; metallo-chaperone; enzyme; metallo-enzyme; metallothionein; Ctr1; Atox1; glutathione; AMYOTROPHIC-LATERAL-SCLEROSIS; CU; ZN SUPEROXIDE-DISMUTASE; N-TERMINAL DOMAIN; ZN-SUPEROXIDE DISMUTASE; CHAPERONE CCS; BIOCHEMICAL-CHARACTERIZATION; MOLECULAR CHARACTERIZATION; TRANSPORTING ATPASES; PHYSIOLOGICAL-ROLE; HUMAN CTR1;
D O I
10.3390/antiox9060500
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
Copper ions (i.e., copper) are a critical part of several cellular processes, but tight regulation of copper levels and trafficking are required to keep the cell protected from this highly reactive transition metal. Cu, Zn superoxide dismutase (Sod1) protects the cell from the accumulation of radical oxygen species by way of the redox cycling activity of copper in its catalytic center. Multiple posttranslational modification events, including copper incorporation, are reliant on the copper chaperone for Sod1 (Ccs). The high-affinity copper uptake protein (Ctr1) is the main entry point of copper into eukaryotic cells and can directly supply copper to Ccs along with other known intracellular chaperones and trafficking molecules. This review explores the routes of copper delivery that are utilized to activate Sod1 and the usefulness and necessity of each.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 50 条
  • [1] Copper activation of superoxide dismutase 1 (SOD1) in vivo -: Role for protein-protein interactions with the copper chaperone for SOD1
    Schmidt, PJ
    Kunst, C
    Culotta, VC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) : 33771 - 33776
  • [2] DJ-1 Is a Copper Chaperone Acting on SOD1 Activation
    Girotto, Stefania
    Cendron, Laura
    Bisaglia, Marco
    Tessari, Isabella
    Mammi, Stefano
    Zanotti, Giuseppe
    Bubacco, Luigi
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (15) : 10887 - 10899
  • [3] Drosophila mutants deficient in CCS, the copper chaperone for SOD1, reveal the role of SOD1 activation in adult lifespan and sensitivity to oxidative stress
    Kirby, Kim
    Binnington, Janet
    Wicks, Shawna
    Anderson, Peter R.
    Hilliker, Arthur J.
    Phillips, John P.
    FREE RADICAL BIOLOGY AND MEDICINE, 2006, 41 : S145 - S145
  • [4] The neuronal adaptor protein X11α interacts with the copper chaperone for SOD1 and regulates SOD1 activity
    McLoughlin, DM
    Standen, CL
    Lau, KF
    Ackerley, S
    Bartnikas, TP
    Gitlin, JD
    Miller, CCJ
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) : 9303 - 9307
  • [5] High fat suppresses SOD1 activity by reducing copper chaperone for SOD1 associated with neurodegeneration and memory decline
    Lu, Ping
    Yan, Hua-Juan
    Yang, Cui
    Feng, Wen-Cai
    Hu, Fei
    Wu, Yue-Ying
    Sun, Wei-Wen
    Gao, Mei-Mei
    Long, Yue-Sheng
    LIFE SCIENCES, 2021, 272
  • [6] Structures of mouse SOD1 and human/mouse SOD1 chimeras
    Seetharaman, Sai V.
    Taylor, Alexander B.
    Holloway, Stephen
    Hart, P. John
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2010, 503 (02) : 183 - 190
  • [7] A gain of superoxide dismutase (SOD) activity obtained with CCS, the copper metallochaperone for SOD1
    Schmidt, PJ
    Ramos-Gomez, M
    Culotta, VC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) : 36952 - 36956
  • [8] SOD1 Gene
    Nithya, K.
    Angeline, T.
    Isabel, W.
    Asirvatham, A. J.
    GENETICS RESEARCH INTERNATIONAL, 2016, 2016
  • [9] Steps to SOD1
    Amy Donner
    Nature Chemical Biology, 2012, 8 (10) : 808 - 808
  • [10] Retinal microglial activation in a SOD1 mouse model of ALS
    Rojas Lozano, Maria Pilar
    Cadena Santoyo, Manuel
    Fernandez-Albarral, Jose A.
    Lopez-Cuenca, Ines
    Salobrar-Garcia, Elena
    De Hoz, Rosa
    Salazar Corral, Juan Jose
    Urcelay Segura, Jose Luis
    Santos-Garcia, Irene
    De lago, Eva
    Manuel Ramirez, Jose
    Isabel Ramirez, Ana
    ACTA OPHTHALMOLOGICA, 2021, 99