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A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease

Paraoxonases (PONs) are a family of hydrolytic enzymes consisting of three members, PON1, PON2, and PON3, located on human chromosome 7. Identifying the physiological substrates of these enzymes is necessary for the elucidation of their biological roles and to establish their applications in the bio...

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Autores principales: Mohammed, Chrysan J., Lamichhane, Sabitri, Connolly, Jacob A., Soehnlen, Sophia M., Khalaf, Fatimah K., Malhotra, Deepak, Haller, Steven T., Isailovic, Dragan, Kennedy, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945423/
https://www.ncbi.nlm.nih.gov/pubmed/35326240
http://dx.doi.org/10.3390/antiox11030590
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author Mohammed, Chrysan J.
Lamichhane, Sabitri
Connolly, Jacob A.
Soehnlen, Sophia M.
Khalaf, Fatimah K.
Malhotra, Deepak
Haller, Steven T.
Isailovic, Dragan
Kennedy, David J.
author_facet Mohammed, Chrysan J.
Lamichhane, Sabitri
Connolly, Jacob A.
Soehnlen, Sophia M.
Khalaf, Fatimah K.
Malhotra, Deepak
Haller, Steven T.
Isailovic, Dragan
Kennedy, David J.
author_sort Mohammed, Chrysan J.
collection PubMed
description Paraoxonases (PONs) are a family of hydrolytic enzymes consisting of three members, PON1, PON2, and PON3, located on human chromosome 7. Identifying the physiological substrates of these enzymes is necessary for the elucidation of their biological roles and to establish their applications in the biomedical field. PON substrates are classified as organophosphates, aryl esters, and lactones based on their structure. While the established native physiological activity of PONs is its lactonase activity, the enzymes’ exact physiological substrates continue to be elucidated. All three PONs have antioxidant potential and play an important anti-atherosclerotic role in several diseases including cardiovascular diseases. PON3 is the last member of the family to be discovered and is also the least studied of the three genes. Unlike the other isoforms that have been reviewed extensively, there is a paucity of knowledge regarding PON3. Thus, the current review focuses on PON3 and summarizes the PON substrates, specific activities, kinetic parameters, and their association with cardiovascular as well as other diseases such as HIV and cancer.
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spelling pubmed-89454232022-03-25 A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease Mohammed, Chrysan J. Lamichhane, Sabitri Connolly, Jacob A. Soehnlen, Sophia M. Khalaf, Fatimah K. Malhotra, Deepak Haller, Steven T. Isailovic, Dragan Kennedy, David J. Antioxidants (Basel) Review Paraoxonases (PONs) are a family of hydrolytic enzymes consisting of three members, PON1, PON2, and PON3, located on human chromosome 7. Identifying the physiological substrates of these enzymes is necessary for the elucidation of their biological roles and to establish their applications in the biomedical field. PON substrates are classified as organophosphates, aryl esters, and lactones based on their structure. While the established native physiological activity of PONs is its lactonase activity, the enzymes’ exact physiological substrates continue to be elucidated. All three PONs have antioxidant potential and play an important anti-atherosclerotic role in several diseases including cardiovascular diseases. PON3 is the last member of the family to be discovered and is also the least studied of the three genes. Unlike the other isoforms that have been reviewed extensively, there is a paucity of knowledge regarding PON3. Thus, the current review focuses on PON3 and summarizes the PON substrates, specific activities, kinetic parameters, and their association with cardiovascular as well as other diseases such as HIV and cancer. MDPI 2022-03-19 /pmc/articles/PMC8945423/ /pubmed/35326240 http://dx.doi.org/10.3390/antiox11030590 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mohammed, Chrysan J.
Lamichhane, Sabitri
Connolly, Jacob A.
Soehnlen, Sophia M.
Khalaf, Fatimah K.
Malhotra, Deepak
Haller, Steven T.
Isailovic, Dragan
Kennedy, David J.
A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title_full A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title_fullStr A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title_full_unstemmed A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title_short A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease
title_sort pon for all seasons: comparing paraoxonase enzyme substrates, activity and action including the role of pon3 in health and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945423/
https://www.ncbi.nlm.nih.gov/pubmed/35326240
http://dx.doi.org/10.3390/antiox11030590
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