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Kinetic Approaches to Measuring Peroxiredoxin Reactivity

Peroxiredoxins are ubiquitous thiol proteins that catalyse the breakdown of peroxides and regulate redox activity in the cell. Kinetic analysis of their reactions is required in order to identify substrate preferences, to understand how molecular structure affects activity and to establish their phy...

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Detalles Bibliográficos
Autores principales: Winterbourn, Christine C., Peskin, Alexander V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749870/
https://www.ncbi.nlm.nih.gov/pubmed/26813658
http://dx.doi.org/10.14348/molcells.2016.2325
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author Winterbourn, Christine C.
Peskin, Alexander V.
author_facet Winterbourn, Christine C.
Peskin, Alexander V.
author_sort Winterbourn, Christine C.
collection PubMed
description Peroxiredoxins are ubiquitous thiol proteins that catalyse the breakdown of peroxides and regulate redox activity in the cell. Kinetic analysis of their reactions is required in order to identify substrate preferences, to understand how molecular structure affects activity and to establish their physiological functions. Various approaches can be taken, including the measurement of rates of individual steps in the reaction pathway by stopped flow or competitive kinetics, classical enzymatic analysis and measurement of peroxidase activity. Each methodology has its strengths and they can often give complementary information. However, it is important to understand the experimental conditions of the assay so as to interpret correctly what parameter is being measured. This brief review discusses different kinetic approaches and the information that can be obtained from them.
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spelling pubmed-47498702016-02-25 Kinetic Approaches to Measuring Peroxiredoxin Reactivity Winterbourn, Christine C. Peskin, Alexander V. Mol Cells Minireview Peroxiredoxins are ubiquitous thiol proteins that catalyse the breakdown of peroxides and regulate redox activity in the cell. Kinetic analysis of their reactions is required in order to identify substrate preferences, to understand how molecular structure affects activity and to establish their physiological functions. Various approaches can be taken, including the measurement of rates of individual steps in the reaction pathway by stopped flow or competitive kinetics, classical enzymatic analysis and measurement of peroxidase activity. Each methodology has its strengths and they can often give complementary information. However, it is important to understand the experimental conditions of the assay so as to interpret correctly what parameter is being measured. This brief review discusses different kinetic approaches and the information that can be obtained from them. Korean Society for Molecular and Cellular Biology 2016-01-31 2016-01-25 /pmc/articles/PMC4749870/ /pubmed/26813658 http://dx.doi.org/10.14348/molcells.2016.2325 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Minireview
Winterbourn, Christine C.
Peskin, Alexander V.
Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title_full Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title_fullStr Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title_full_unstemmed Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title_short Kinetic Approaches to Measuring Peroxiredoxin Reactivity
title_sort kinetic approaches to measuring peroxiredoxin reactivity
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749870/
https://www.ncbi.nlm.nih.gov/pubmed/26813658
http://dx.doi.org/10.14348/molcells.2016.2325
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