Quantification and significance of protein oxidation in biological samples

被引:602
作者
Shacter, E [1 ]
机构
[1] US FDA, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
关键词
protein oxidation; disease; oxidative stress; markers; methods; therapeutic proteins;
D O I
10.1081/DMR-100102336
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein oxidation is defined here as the covalent modification of a protein induced either directly by reactive oxygen species or indirectly by reaction with secondary by-products of oxidative stress. Oxidative modification of proteins can be induced experimentally by a wide array of prooxidant agents and occurs in vivo during aging and in certain disease conditions. Oxidative changes to proteins can lead to diverse functional consequences, such as inhibition of enzymatic and binding activities, increased susceptibility to aggregation and proteolysis, increased or decreased uptake by cells, and altered immunogenicity. There are numerous types of protein oxidative modification and these can be measured with a variety of methods. Protein oxidation serves as a useful marker for assessing oxidative stress in vivo. There are both advantages and disadvantages to using proteins for this purpose compared to lipids and DNA. Finally, it is important to monitor the degree of oxidative modification of therapeutic proteins manufactured for commercial use. This review will examine various aspects of protein oxidation, with emphasis on using proteins as markers of oxidative stress in biological samples.
引用
收藏
页码:307 / 326
页数:20
相关论文
共 130 条
[11]   CARBONIC ANHYDRASE-III - OXIDATIVE MODIFICATION IN-VIVO AND LOSS OF PHOSPHATASE-ACTIVITY DURING AGING [J].
CABISCOL, E ;
LEVINE, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14742-14747
[12]   REVERSAL OF AGE-RELATED INCREASE IN BRAIN PROTEIN OXIDATION, DECREASE IN ENZYME-ACTIVITY, AND LOSS IN TEMPORAL AND SPATIAL MEMORY BY CHRONIC ADMINISTRATION OF THE SPIN-TRAPPING COMPOUND N-TERT-BUTYL-ALPHA-PHENYLNITRONE [J].
CARNEY, JM ;
STARKEREED, PE ;
OLIVER, CN ;
LANDUM, RW ;
CHENG, MS ;
WU, JF ;
FLOYD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3633-3636
[13]   POTENTIAL MECHANISM OF EMPHYSEMA - ALPHA-1-PROTEINASE INHIBITOR RECOVERED FROM LUNGS OF CIGARETTE SMOKERS CONTAINS OXIDIZED METHIONINE AND HAS DECREASED ELASTASE INHIBITORY CAPACITY [J].
CARP, H ;
MILLER, F ;
HOIDAL, JR ;
JANOFF, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :2041-2045
[14]   Modification of cysteine residues in vitro and in vivo affects the immunogenicity and antigenicity of major histocompatibility complex class I-restricted viral determinants [J].
Chen, WS ;
Yewdell, JW ;
Levine, RL ;
Bennink, JR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (11) :1757-1764
[15]   Modification of proteins in endothelial cell death during oxidative stress [J].
Ciolino, HP ;
Levine, RL .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (07) :1277-1282
[16]   OXIDATIVE DAMAGE TO HUMAN PLASMA-PROTEINS BY OZONE [J].
CROSS, CE ;
REZNICK, AZ ;
PACKER, L ;
DAVIS, PA ;
SUZUKI, YJ ;
HALLIWELL, B .
FREE RADICAL RESEARCH COMMUNICATIONS, 1992, 15 (06) :347-352
[17]  
CZAPSKI G, 1984, ISR J CHEM, V24, P29
[18]  
DAVIES KJA, 1987, J BIOL CHEM, V262, P9895
[19]  
DAVIES KJA, 1990, ADV EXP MED BIOL, V264, P503
[20]  
DAVIES KJA, 1987, J BIOL CHEM, V262, P9908