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Oligomerization of Cu,Zn-Superoxide Dismutase (SOD1) by Docosahexaenoic Acid and Its Hydroperoxides In Vitro: Aggregation Dependence on Fatty Acid Unsaturation and Thiols
by
Cussiol, José Renato Rosa
, Netto, Luis Eduardo Soares
, Chaves-Filho, Adriano B.
, Miyamoto, Sayuri
, Appolinário, Patricia Postilione
, Genaro-Mattos, Thiago C.
, Medinas, Danilo Bilches
, Augusto, Ohara
in
Agglomeration
/ Amyloid
/ Amyotrophic lateral sclerosis
/ Brain
/ Chromatography, Gel
/ Copper
/ Dependence
/ Dimerization
/ Docosahexaenoic acid
/ Docosahexaenoic Acids - metabolism
/ Electrophoresis, Polyacrylamide Gel
/ Enzymes
/ Fatty acids
/ Fatty Acids - metabolism
/ Humans
/ Hydrogen Peroxide - metabolism
/ Hydrophobicity
/ Incubation
/ Lipids
/ Low molecular weights
/ Molecular modelling
/ Molecular weight
/ Mutation
/ Oligomerization
/ Oligomers
/ Omega 3 fatty acids
/ Oxidation
/ Polyunsaturated fatty acids
/ Protein Multimerization
/ Protein structure
/ Proteins
/ Site-directed mutagenesis
/ Species
/ Sulfhydryl Compounds - metabolism
/ Superoxide dismutase
/ Superoxide Dismutase - chemistry
/ Superoxide Dismutase - metabolism
/ Superoxides
/ Thiols
/ Unsaturated fatty acids
/ Zinc
/ Zinc (Metal)
/ Zinc compounds
2015
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Oligomerization of Cu,Zn-Superoxide Dismutase (SOD1) by Docosahexaenoic Acid and Its Hydroperoxides In Vitro: Aggregation Dependence on Fatty Acid Unsaturation and Thiols
by
Cussiol, José Renato Rosa
, Netto, Luis Eduardo Soares
, Chaves-Filho, Adriano B.
, Miyamoto, Sayuri
, Appolinário, Patricia Postilione
, Genaro-Mattos, Thiago C.
, Medinas, Danilo Bilches
, Augusto, Ohara
in
Agglomeration
/ Amyloid
/ Amyotrophic lateral sclerosis
/ Brain
/ Chromatography, Gel
/ Copper
/ Dependence
/ Dimerization
/ Docosahexaenoic acid
/ Docosahexaenoic Acids - metabolism
/ Electrophoresis, Polyacrylamide Gel
/ Enzymes
/ Fatty acids
/ Fatty Acids - metabolism
/ Humans
/ Hydrogen Peroxide - metabolism
/ Hydrophobicity
/ Incubation
/ Lipids
/ Low molecular weights
/ Molecular modelling
/ Molecular weight
/ Mutation
/ Oligomerization
/ Oligomers
/ Omega 3 fatty acids
/ Oxidation
/ Polyunsaturated fatty acids
/ Protein Multimerization
/ Protein structure
/ Proteins
/ Site-directed mutagenesis
/ Species
/ Sulfhydryl Compounds - metabolism
/ Superoxide dismutase
/ Superoxide Dismutase - chemistry
/ Superoxide Dismutase - metabolism
/ Superoxides
/ Thiols
/ Unsaturated fatty acids
/ Zinc
/ Zinc (Metal)
/ Zinc compounds
2015
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Oligomerization of Cu,Zn-Superoxide Dismutase (SOD1) by Docosahexaenoic Acid and Its Hydroperoxides In Vitro: Aggregation Dependence on Fatty Acid Unsaturation and Thiols
by
Cussiol, José Renato Rosa
, Netto, Luis Eduardo Soares
, Chaves-Filho, Adriano B.
, Miyamoto, Sayuri
, Appolinário, Patricia Postilione
, Genaro-Mattos, Thiago C.
, Medinas, Danilo Bilches
, Augusto, Ohara
in
Agglomeration
/ Amyloid
/ Amyotrophic lateral sclerosis
/ Brain
/ Chromatography, Gel
/ Copper
/ Dependence
/ Dimerization
/ Docosahexaenoic acid
/ Docosahexaenoic Acids - metabolism
/ Electrophoresis, Polyacrylamide Gel
/ Enzymes
/ Fatty acids
/ Fatty Acids - metabolism
/ Humans
/ Hydrogen Peroxide - metabolism
/ Hydrophobicity
/ Incubation
/ Lipids
/ Low molecular weights
/ Molecular modelling
/ Molecular weight
/ Mutation
/ Oligomerization
/ Oligomers
/ Omega 3 fatty acids
/ Oxidation
/ Polyunsaturated fatty acids
/ Protein Multimerization
/ Protein structure
/ Proteins
/ Site-directed mutagenesis
/ Species
/ Sulfhydryl Compounds - metabolism
/ Superoxide dismutase
/ Superoxide Dismutase - chemistry
/ Superoxide Dismutase - metabolism
/ Superoxides
/ Thiols
/ Unsaturated fatty acids
/ Zinc
/ Zinc (Metal)
/ Zinc compounds
2015
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Oligomerization of Cu,Zn-Superoxide Dismutase (SOD1) by Docosahexaenoic Acid and Its Hydroperoxides In Vitro: Aggregation Dependence on Fatty Acid Unsaturation and Thiols
Journal Article
Oligomerization of Cu,Zn-Superoxide Dismutase (SOD1) by Docosahexaenoic Acid and Its Hydroperoxides In Vitro: Aggregation Dependence on Fatty Acid Unsaturation and Thiols
2015
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Overview
Docosahexaenoic acid (C22:6, n-3, DHA) is a polyunsaturated fatty acid highly enriched in the brain. This fatty acid can be easily oxidized yielding hydroperoxides as primary products. Cu, Zn-Superoxide dismutase (SOD1) aggregation is a common hallmark of Amyotrophic Lateral Sclerosis (ALS) and the molecular mechanisms behind their formation are not completely understood. Here we investigated the effect of DHA and its hydroperoxides (DHAOOH) on human SOD1 oligomerization in vitro. DHA induced the formation of high-molecular-weight (HMW) SOD1 species (>700 kDa). Aggregation was dependent on free thiols and occurred primarily with the protein in its apo-form. SOD1 incubation with DHA was accompanied by changes in protein structure leading to exposure of protein hydrophobic patches and formation of non-amyloid aggregates. Site-directed mutagenesis studies demonstrated that Cys 6 and Cys 111 in wild-type and Cys 6 in ALS-linked G93A mutant are required for aggregation. In contrast, DHAOOH did not induce HMW species formation but promoted abnormal covalent dimerization of apo-SOD1 that was resistant to SDS and thiol reductants. Overall, our data demonstrate that DHA and DHAOOH induce distinct types of apo-SOD1 oligomerization leading to the formation of HMW and low-molecular-weight species, respectively.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Amyloid
/ Amyotrophic lateral sclerosis
/ Brain
/ Copper
/ Docosahexaenoic Acids - metabolism
/ Electrophoresis, Polyacrylamide Gel
/ Enzymes
/ Humans
/ Hydrogen Peroxide - metabolism
/ Lipids
/ Mutation
/ Proteins
/ Species
/ Sulfhydryl Compounds - metabolism
/ Superoxide Dismutase - chemistry
/ Superoxide Dismutase - metabolism
/ Thiols
/ Zinc
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