360 likes | 801 Views
Oxidative Stress Concepts. Graduate Course 2214/938 (KI/UNL) June 14, 2010. Donald Becker Redox Biology Center University of Nebraska. Disease and Aging. Rate of living hypothesis- states metabolic rate of species determines its life-time.
E N D
Oxidative Stress Concepts Graduate Course 2214/938 (KI/UNL) June 14, 2010 Donald Becker Redox Biology Center University of Nebraska
Disease and Aging Rate of living hypothesis- states metabolic rate of species determines its life-time. 1950’s Dr. Harman (University of Nebraska Medical School) speculated the “free radical” theory of ageing results in a pattern of cumulative damage. Free radicals involving oxygen have been renamed as reactive oxygen species (ROS) and encompass a variety of diverse chemical species including superoxide anions, hydroxyl radicals, and hydrogen peroxide.
Outline • Sources ROS (environmental, metabolic, immune system) • Damage that ROS causes • Defenses against ROS (enzymes, small molecules, reaction rates) • 4. Mechanisms of stress response
Overview of ROS Toren Finkel* & Nikki J. Holbrook. (2000) Nature 408, 239-247.
ROS sources for bacteria environmental NADPH oxidase (phagosome) Competing microbes (pyruvate oxidase) antibiotics Imlay, Ann. Rev. Biochem. 2008, 77:755-776.
NADPH L-Arg NOS NADP+ •NO O2•- ONOO- (peroxynitrite) ROS sources in mammalian cells • Mitochondrial respiration • Byproducts of enzyme activity (flavin enzymes, xanthine oxidase) • Nitric Oxide Synthase • Peroxisomal and endoplasmic reticulum processes • NADPH oxidases (NOXs) • Environmental-UV radiation, redox cycling (P450)
Sites of mitochondrial ROS formation ROS-site Km (O2) uM Complex I flavin 0.2 Complex I QH 0.9 Complex III QH 2.0 ETF QH 5.0 Hoffman and Brookes, JBC, 284, pp. 16236–16245, 2009.
ROS generation by NADPH Oxidases Neutrophil phagosome Receptor mediated (smooth muscle cells) (contain flavin and cytochrome b) Winterbourn, NATURE CHEMICAL BIOLOGY, 4, 278-286, 2008.
Estimated diffusion distances of ROS 2 mM GSH present GSH reaction rate constants (M-1 s-1) H2O2 0.9 ONOO- 700 HOCl 3x107 •NO2 3x107 •HO 1x1010 Winterbourn, NATURE CHEMICAL BIOLOGY, 4, 278-286, 2008.
Targets of ROS Toledano, Nat Rev Mol Cell Biol, 8:813-824, 2007.
DNA Damage 7,8-Dihydro-8-oxo-2’-deoxyguanosine (OG) arises from oxidation of guanine. Guanidinohydantoin (Gh) and spiroiminodihydantoin (Sp) arise either directly from oxidation of guanine or from further oxidation of OG. Thymine glycol (Tg) arises from oxidation of thymine. All of these base lesions are repaired by the base excision repair pathway. (David, Chap.3, Redox Biochemistry)
Protein modifications by ROS Stadtman, Chapter 5, Redox Biochemistry
Frequency of modification by ROS Regnier, Journal of Proteome Research 2006, 5, 2159-2168
Cellular distribution of ROS damaged proteins Regnier, Journal of Proteome Research 2006, 5, 2159-2168
Protection against ROS • Metal sequestration & efflux • Ferritin • Small molecules • glutathione, ascorbic acid, beta-carotene, tocopherol, flavonoids • - Scavenge reactive oxygen species • Antioxidant enzymes- catalase (Cat), superoxide dismutase (SOD), peroxiredoxins (Prx), alkyl hydroperoxide reductases (Ahp), thioredoxin (Trx), thioredoxin reductase (TrxR), glutathione reductase (GR), glutathione peroxidase (Gpx), glutaredoxin (Grx) • DNA and protein damage repair enzymes • Base excision repair enzymes (glycosylase) • Sulfiredoxins (reduces cysteine sulfinic acid, R-SO2H) • Methionine sulfoxide reductases • -Detoxify (xenobiotics) • Glutathione-S-transferase, Cytochrome P450 enzymes
Defenses against ROS Beal, Nature. 2006 Oct 19;443(7113):787-95.
(60 uM) (2 uM) (20 uM) (2 uM) (1.4 nM) (5 mM) Is Peroxiredoxin 3 the major H2O2 scavenger in mitochondria? k (T)=k(target) * [target] Hampton, Biochem. J. (2010) 425, 313–325
Prx3 Prx5 Catalytic Cycles of Prx Prx vs Cat Km (H2O2) lower (uM) higher (mM) kcat lower (1-80 s-1) higher (104 s-1) kcat/Km 104-107 M-1s-1 106-107 M-1s-1 Hampton, Biochem. J. (2010) 425, 313–325
Unique roles of H2O2 and Cysteine in ROS signaling Oxidation of Cys residues as the basis for peroxide signaling Toledano, Nat Rev Mol Cell Biol, 8:813-824, 2007.
Bacterial sensors PerR
Yap1 Sensor in yeast With increases in H2O2, Gpx3 catalyzes the oxidation of cysteine residues in Yap1 resulting in disulfide bond. Oxidized Yap1 then accumulates in the nucleus where it activates the transcription of antioxidant genes. Finkel, Circ. Res. 2005;97;967-974
Sensors in mammalians ROS Change intracellular location Keap1/Nrf2 Keap1 Under normal conditions, Keap1 (cytosolic) interacts with Nrf2 (a transcription factor) to keep it sequestered in the cytosol. This interaction also helps target Nrf2 for proteasomal degradation. With increases in ROS, cysteine residues in Keap1 are oxidized which leads to disulfide bond formation, zinc release, and a conformational change. As a result, Nrf2 is released from Keap1 and enters the nucleus. Thus, the oxidation of Keap1 triggers Nrf2 to accumulate in the nucleus and activate antioxidant functions in the cell (antioxidant responsive elements). Finkel, Circ. Res. 2005;97;967-974
H2O2 signaling Chapter 4, Redox Biochemistry Book
CO is an important regulator of hypoxic sensing by the carotid body
Summary • ROS sources involve metabolism, environmental factors, and immune response • ROS (hydroxyl radicals) induces damage to a variety of biomolecules • A robust antioxidant system helps maintain proper ROS levels (peroxiredoxin) • Specific sensors for ROS that turn on transcriptional responses have cysteine and/or metal based centers • Reactivity of cysteine residues are tuned by the protein • Hydrogen peroxide is an important ROS signaling molecule