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https://hdl.handle.net/2440/69717
Type: | Thesis |
Title: | The functional and molecular consequences of oxidation in the skeletal muscle myofilament. |
Author: | Spencer, Timothy |
Issue Date: | 2011 |
School/Discipline: | School of Medical Sciences |
Abstract: | It is becoming increasingly evident that redox state leading to post-translational modifications of structural proteins, enzymes and ion channels can cause activation or inhibition of cellular function (Andrade et al., 1998a, Jackson, 2008, Kelly et al., 1996). While low levels of nitric oxide (NO) synthesised by endothelial and neuronal nitric oxide synthase have been shown to provide a beneficial effect to tissues, the elevated release of NO accompanying inflammation has a detrimental effect, resulting in dysfunction (Khanna et al., 2005). We investigated the functional consequence and molecular substrate of NO and another potentially harmful reactive oxygen species, H ₂O ₂, on the skeletal muscle myofilament. In a rat model we used functional myography of demembranated single fast- and slow-twitch skeletal muscle fibers to examined the consequence of the addition of the free radical NO and reactive oxygen species H₂O₂ on the Ca²⁺ sensitivity of the myofilament. The reversibility of oxidative modifications following NO or H ₂O ₂ treatment was examined using the general anti-oxidant dithiothreitol. Isoelectric focusing combined with SDS-PAGE separation of proteins investigated the post-translational modification of free-radical exposed myofilament proteins. Molecular substitution of endogenous troponin C (TnC) with WT cardiac/slow TnC or C84S TnC, incapable of being oxidized at Cys84, investigated the molecular and functional consequence of oxidation of TnC at Cys84. Exposure of fast-twitch muscle fibers to NO resulted in a decrease in Ca²⁺ sensitivity, while H ₂O ₂ had the opposite effect, increasing Ca²⁺ sensitivity. In contrast, slow-twitch fibers were insensitive to both NO and H ₂O ₂. Following myofilament exposure to NO (~2 uM) proteomic analysis revealed that many proteins underwent post-translational modification, including myosin light chain (LC ₂₀) and TnC. Molecular substitution of endogenous fast-twitch TnC with WT-cardiac/slow TnC demonstrated a similar sensitivity to NO as WT skeletal muscle. In contrast TnC, non-oxidizable at Cys84, rendered fast-twitch skeletal muscle insensitive to NO. Many myofilament proteins, including myosin light chains were identified as being post-translationally modified by NO exposure, however, molecular substitution experiments clearly identify TnC, specifically residue Cys84 as the functional substrate responsible for fast-twitch skeletal muscle sensitivity to NO. Although slow-twitch muscle contains the same isoform of TnC, it was insensitive to NO. This suggests that slow-twitch muscle may have a greater capacity for anti-oxidant defense than fast-twitch muscle. The contrasting increase in Ca²⁺ sensitivity following H ₂O ₂ to the decline caused by NO demonstrates that not all oxidative molecules act alike, possibly targeting differing substrates and causing differing post-translational modifications. |
Advisor: | Wilson, David |
Dissertation Note: | Thesis (Ph.D.) -- University of Adelaide, School of Medical Sciences, 2011 |
Keywords: | nitric oxide; nitroso-glutathione; reactive oxygen species; hydrogen peroxide; troponin |
Provenance: | Copyright material removed from digital thesis. See print copy in University of Adelaide Library for full text. |
Appears in Collections: | Research Theses |
Files in This Item:
File | Description | Size | Format | |
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01front.pdf | 181.72 kB | Adobe PDF | View/Open | |
02whole.pdf | 1.26 MB | Adobe PDF | View/Open |
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