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Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions
To understand oxidative stress, antioxidant defense, and redox signaling in health and disease it is essential to assess protein thiol redox state. Protein thiol redox state is seldom assessed immunologically because of the inability to distinguish reduced and reversibly oxidized thiols by Western b...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222201/ https://www.ncbi.nlm.nih.gov/pubmed/32326525 http://dx.doi.org/10.3390/antiox9040315 |
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author | Cobley, James Nathan Husi, Holger |
author_facet | Cobley, James Nathan Husi, Holger |
author_sort | Cobley, James Nathan |
collection | PubMed |
description | To understand oxidative stress, antioxidant defense, and redox signaling in health and disease it is essential to assess protein thiol redox state. Protein thiol redox state is seldom assessed immunologically because of the inability to distinguish reduced and reversibly oxidized thiols by Western blotting. An underappreciated opportunity exists to use Click PEGylation to realize the transformative power of simple, time and cost-efficient immunological techniques. Click PEGylation harnesses selective, bio-orthogonal Click chemistry to separate reduced and reversibly oxidized thiols by selectively ligating a low molecular weight polyethylene glycol moiety to the redox state of interest. The resultant ability to disambiguate reduced and reversibly oxidized species by Western blotting enables Click PEGylation to assess protein thiol redox state. In the present review, to enable investigators to effectively harness immunological techniques to assess protein thiol redox state we critique the chemistry, promise and challenges of Click PEGylation. |
format | Online Article Text |
id | pubmed-7222201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72222012020-05-28 Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions Cobley, James Nathan Husi, Holger Antioxidants (Basel) Review To understand oxidative stress, antioxidant defense, and redox signaling in health and disease it is essential to assess protein thiol redox state. Protein thiol redox state is seldom assessed immunologically because of the inability to distinguish reduced and reversibly oxidized thiols by Western blotting. An underappreciated opportunity exists to use Click PEGylation to realize the transformative power of simple, time and cost-efficient immunological techniques. Click PEGylation harnesses selective, bio-orthogonal Click chemistry to separate reduced and reversibly oxidized thiols by selectively ligating a low molecular weight polyethylene glycol moiety to the redox state of interest. The resultant ability to disambiguate reduced and reversibly oxidized species by Western blotting enables Click PEGylation to assess protein thiol redox state. In the present review, to enable investigators to effectively harness immunological techniques to assess protein thiol redox state we critique the chemistry, promise and challenges of Click PEGylation. MDPI 2020-04-15 /pmc/articles/PMC7222201/ /pubmed/32326525 http://dx.doi.org/10.3390/antiox9040315 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Cobley, James Nathan Husi, Holger Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title | Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title_full | Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title_fullStr | Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title_full_unstemmed | Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title_short | Immunological Techniques to Assess Protein Thiol Redox State: Opportunities, Challenges and Solutions |
title_sort | immunological techniques to assess protein thiol redox state: opportunities, challenges and solutions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222201/ https://www.ncbi.nlm.nih.gov/pubmed/32326525 http://dx.doi.org/10.3390/antiox9040315 |
work_keys_str_mv | AT cobleyjamesnathan immunologicaltechniquestoassessproteinthiolredoxstateopportunitieschallengesandsolutions AT husiholger immunologicaltechniquestoassessproteinthiolredoxstateopportunitieschallengesandsolutions |