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A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae

Genetically encoded fluorescent H(2)O(2) probes continue to advance the field of redox biology. Here, we compare the previously established peroxiredoxin-based H(2)O(2) probe roGFP2-Tsa2ΔC(R) with the newly described OxyR-based H(2)O(2) probe HyPer7, using yeast as the model system. Although not as...

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Autores principales: Kritsiligkou, Paraskevi, Shen, Tzu Keng, Dick, Tobias P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274284/
https://www.ncbi.nlm.nih.gov/pubmed/34118234
http://dx.doi.org/10.1016/j.jbc.2021.100866
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author Kritsiligkou, Paraskevi
Shen, Tzu Keng
Dick, Tobias P.
author_facet Kritsiligkou, Paraskevi
Shen, Tzu Keng
Dick, Tobias P.
author_sort Kritsiligkou, Paraskevi
collection PubMed
description Genetically encoded fluorescent H(2)O(2) probes continue to advance the field of redox biology. Here, we compare the previously established peroxiredoxin-based H(2)O(2) probe roGFP2-Tsa2ΔC(R) with the newly described OxyR-based H(2)O(2) probe HyPer7, using yeast as the model system. Although not as sensitive as roGFP2-Tsa2ΔC(R), HyPer7 is much improved relative to earlier HyPer versions, most notably by ratiometric pH stability. The most striking difference between the two probes is the dynamics of intracellular probe reduction. HyPer7 is rapidly reduced, predominantly by the thioredoxin system, whereas roGFP2-Tsa2ΔC(R) is reduced more slowly, predominantly by the glutathione system. We discuss the pros and cons of each probe and suggest that future side-by-side measurements with both probes may provide information on the relative activity of the two major cellular reducing systems.
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spelling pubmed-82742842021-07-16 A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae Kritsiligkou, Paraskevi Shen, Tzu Keng Dick, Tobias P. J Biol Chem Research Article Genetically encoded fluorescent H(2)O(2) probes continue to advance the field of redox biology. Here, we compare the previously established peroxiredoxin-based H(2)O(2) probe roGFP2-Tsa2ΔC(R) with the newly described OxyR-based H(2)O(2) probe HyPer7, using yeast as the model system. Although not as sensitive as roGFP2-Tsa2ΔC(R), HyPer7 is much improved relative to earlier HyPer versions, most notably by ratiometric pH stability. The most striking difference between the two probes is the dynamics of intracellular probe reduction. HyPer7 is rapidly reduced, predominantly by the thioredoxin system, whereas roGFP2-Tsa2ΔC(R) is reduced more slowly, predominantly by the glutathione system. We discuss the pros and cons of each probe and suggest that future side-by-side measurements with both probes may provide information on the relative activity of the two major cellular reducing systems. American Society for Biochemistry and Molecular Biology 2021-06-09 /pmc/articles/PMC8274284/ /pubmed/34118234 http://dx.doi.org/10.1016/j.jbc.2021.100866 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Kritsiligkou, Paraskevi
Shen, Tzu Keng
Dick, Tobias P.
A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title_full A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title_fullStr A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title_full_unstemmed A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title_short A comparison of Prx- and OxyR-based H(2)O(2) probes expressed in S. cerevisiae
title_sort comparison of prx- and oxyr-based h(2)o(2) probes expressed in s. cerevisiae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274284/
https://www.ncbi.nlm.nih.gov/pubmed/34118234
http://dx.doi.org/10.1016/j.jbc.2021.100866
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