Impact of hydrogen peroxide on structure, stability, and aggregational properties of human γS-crystallin

被引:0
|
作者
Vendra, Venkata Pulla Rao [1 ]
机构
[1] NEI, NIH, Ophthalm Genet & Visual Funct Branch, Ophthalm Mol Genet Sect, Bethesda, MD 20892 USA
关键词
Aggregation; cataract; crystallins; eye lens; H2O2; oxidative stress; OXIDATIVE STRESS; LENS; CATARACT; H2O2; ACTIVATION; MECHANISM; PROTEINS; DAMAGE; GENES;
D O I
10.1007/s12038-023-00330-w
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cataract is the leading cause of blindness worldwide. Oxidative stress is one of the known risk factors for age-related cataracts. The present study was designed to understand the effect of H2O2-induced oxidative stress on human gamma S-crystallin and its relationship to lens opacification and cataract. Human gamma S-crystallin cDNA was cloned into the pET-20b vector, overexpressed in BL21 Star (DE3) cells, and was purified using ion-exchange and gel filtration chromatography. The structure, stability, and aggregational properties of human gamma S-crystallin under H2O2 stress were studied using fluorescence and circular dichroism spectroscopy methods. H2O2 treatment did not show any significant effect on the gamma S-crystallin secondary structure but showed an effect on its tertiary structure, resulting in N '-formylkynurenine formation. The H2O2-treated sample showed increased surface hydrophobicity, was less stable, and opened its Greek key motifs earlier with a midpoint of thermal unfolding curve (T-m) of 70.2 degrees C compared with untreated gamma S-crystallin (T-m=71.4 degrees C). The sample treated with H2O2 aggregated earlier in response to heating at 65 degrees C. H2O2-induced oxidative stress alters the tryptophan microenvironment and the surface hydrophobicity of gamma S-crystallin, and these changes decrease its thermal stability and increase its tendency to aggregate, consistent with its role as a risk factor in age-related cataract.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Impact of Hydrogen Peroxide on the Activity, Structure, and Conformational Stability of the Oxidized Protein Repair Enzyme Methionine Sulfoxide Reductase A
    Le, Hai-Tuong
    Chaffotte, Alain F.
    Demey-Thomas, Ernmanuelle
    Vinh, Joeelle
    Friguet, Bertrand
    Mary, Jean
    JOURNAL OF MOLECULAR BIOLOGY, 2009, 393 (01) : 58 - 66
  • [42] Deamidation alters the structure and decreases the stability of human lens βΑ3-crystallin
    Takata, Takumi
    Oxford, Julie T.
    Brandon, Theodore R.
    Lampi, Kirsten J.
    BIOCHEMISTRY, 2007, 46 (30) : 8861 - 8871
  • [43] Effect of pH, hydrogen peroxide and temperature on the stability of human monoclonal antibody
    Usami, A
    Ohtsu, A
    Takahama, S
    Fujii, T
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1996, 14 (8-10) : 1133 - 1140
  • [44] Explosive Properties and Thermal Stability of Urea-Hydrogen Peroxide Adduct
    Matyas, Robert
    Selesovsky, Jakub
    Pelikan, Vojtech
    Szala, Mateusz
    Cudzilo, Stanislaw
    Trzcinski, Waldemar A.
    Gozin, Michael
    PROPELLANTS EXPLOSIVES PYROTECHNICS, 2017, 42 (02) : 198 - 203
  • [45] INFLUENCE OF HYDROGEN-PEROXIDE TO CHEMICAL STRUCTURE OF HUMAN HAIR
    ERLEMANN, GA
    BEYER, H
    JOURNAL OF THE SOCIETY OF COSMETIC CHEMISTS, 1971, 22 (12): : 795 - &
  • [46] Cataract-causing G18V eliminates the antagonization by ATP against the crowding-induced destabilization of human γS-crystallin
    He, Yuan
    Kang, Jian
    Song, Jianxing
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2020, 530 (03) : 554 - 560
  • [47] Structure of a Highly Active Cephalopod S-crystallin Mutant: New Molecular Evidence for Evolution from an Active Enzyme into Lens-Refractive Protein
    Tan, Wei-Hung
    Cheng, Shu-Chun
    Liu, Yu-Tung
    Wu, Cheng-Guo
    Lin, Min-Han
    Chen, Chiao-Che
    Lin, Chao-Hsiung
    Chou, Chi-Yuan
    SCIENTIFIC REPORTS, 2016, 6
  • [48] PRIMARY STRUCTURE OF BETA-S-CRYSTALLIN FROM HUMAN LENS
    ZARINA, S
    ABBASI, A
    ZAIDI, ZH
    BIOCHEMICAL JOURNAL, 1992, 287 : 375 - 381
  • [49] Structure of a Highly Active Cephalopod S-crystallin Mutant: New Molecular Evidence for Evolution from an Active Enzyme into Lens-Refractive Protein
    Wei-Hung Tan
    Shu-Chun Cheng
    Yu-Tung Liu
    Cheng-Guo Wu
    Min-Han Lin
    Chiao-Che Chen
    Chao-Hsiung Lin
    Chi-Yuan Chou
    Scientific Reports, 6
  • [50] Influence of hydrogen peroxide on the stability and optical properties of Cd Squantum dots in gelatin
    Klyuev, V. G.
    Volykhin, D. V.
    Ivanova, A. A.
    JOURNAL OF LUMINESCENCE, 2017, 183 : 519 - 524