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Evaluating peroxiredoxin sensitivity towards inactivation by peroxide substrates Pubblico Deposited

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https://ir.library.oregonstate.edu/concern/articles/c534fp769

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Abstract
  • Peroxiredoxins (Prxs) are very effective peroxide reducing enzymes, but also are susceptible to being oxidatively inactivated by their own substrates. The level of sensitivity to such hyperoxidation varies depending both on the enzyme involved and the type of peroxide substrate. For some Prxs, the hyperoxidation has physiological relevance, so it is important to define approaches that can be used to quantify sensitivity. Here we describe three distinct approaches that can be used to obtain quantitative or semiquantitative estimates of Prx sensitivity and define C[subscript hyp1%] as a simple way of quantifying sensitivity so that values can easily be compared.
  • Keywords: mass spectrometry, cysteine sulfenic acid, oxidative inactivation, peroxidase, cysteine sulfinic acid, peroxide signaling, redox signaling, hyperoxidation
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Citation
  • Nelson, K. J, Parsonage, D., Karplus, P. A., & Poole, L. B. (2013). Evaluating peroxiredoxin sensitivity toward inactivation by peroxide substrates. Methods in Enzymology 527: 21-40. doi:10.1016/B978-0-12-405882-8.00002-7
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  • 527
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  • This work was supported by U. S. Public Health Service Grant GM050389 from the National Institutes of Health and by a 2011 Spark drug discovery grant from Wake Forest School of Medicine.
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