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Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions

ABSTRACT: Metabolites produced via traditional biochemical processes affect intracellular communication, inflammation, and malignancy. Unexpectedly, acetyl-CoA, α-ketoglutarate and palmitic acid, which are chemical species of reactions catalyzed by highly abundant, gigantic enzymatic complexes, dubb...

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Autores principales: Skalidis, Ioannis, Tüting, Christian, Kastritis, Panagiotis L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448341/
https://www.ncbi.nlm.nih.gov/pubmed/32843078
http://dx.doi.org/10.1186/s12964-020-00631-9
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author Skalidis, Ioannis
Tüting, Christian
Kastritis, Panagiotis L.
author_facet Skalidis, Ioannis
Tüting, Christian
Kastritis, Panagiotis L.
author_sort Skalidis, Ioannis
collection PubMed
description ABSTRACT: Metabolites produced via traditional biochemical processes affect intracellular communication, inflammation, and malignancy. Unexpectedly, acetyl-CoA, α-ketoglutarate and palmitic acid, which are chemical species of reactions catalyzed by highly abundant, gigantic enzymatic complexes, dubbed as “metabolons”, have broad “nonmetabolic” signaling functions. Conserved unstructured regions within metabolons determine the yield of these metabolites. Unstructured regions tether functional protein domains, act as spatial constraints to confine constituent enzyme communication, and, in the case of acetyl-CoA production, tend to be regulated by intricate phosphorylation patterns. This review presents the multifaceted roles of these three significant metabolites and describes how their perturbation leads to altered or transformed cellular function. Their dedicated enzymatic systems are then introduced, namely, the pyruvate dehydrogenase (PDH) and oxoglutarate dehydrogenase (OGDH) complexes, and the fatty acid synthase (FAS), with a particular focus on their structural characterization and the localization of unstructured regions. Finally, upstream metabolite regulation, in which spatial occupancy of unstructured regions within dedicated metabolons may affect metabolite availability and subsequently alter cell functions, is discussed. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-74483412020-08-27 Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions Skalidis, Ioannis Tüting, Christian Kastritis, Panagiotis L. Cell Commun Signal Review ABSTRACT: Metabolites produced via traditional biochemical processes affect intracellular communication, inflammation, and malignancy. Unexpectedly, acetyl-CoA, α-ketoglutarate and palmitic acid, which are chemical species of reactions catalyzed by highly abundant, gigantic enzymatic complexes, dubbed as “metabolons”, have broad “nonmetabolic” signaling functions. Conserved unstructured regions within metabolons determine the yield of these metabolites. Unstructured regions tether functional protein domains, act as spatial constraints to confine constituent enzyme communication, and, in the case of acetyl-CoA production, tend to be regulated by intricate phosphorylation patterns. This review presents the multifaceted roles of these three significant metabolites and describes how their perturbation leads to altered or transformed cellular function. Their dedicated enzymatic systems are then introduced, namely, the pyruvate dehydrogenase (PDH) and oxoglutarate dehydrogenase (OGDH) complexes, and the fatty acid synthase (FAS), with a particular focus on their structural characterization and the localization of unstructured regions. Finally, upstream metabolite regulation, in which spatial occupancy of unstructured regions within dedicated metabolons may affect metabolite availability and subsequently alter cell functions, is discussed. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2020-08-26 /pmc/articles/PMC7448341/ /pubmed/32843078 http://dx.doi.org/10.1186/s12964-020-00631-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Skalidis, Ioannis
Tüting, Christian
Kastritis, Panagiotis L.
Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title_full Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title_fullStr Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title_full_unstemmed Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title_short Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
title_sort unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448341/
https://www.ncbi.nlm.nih.gov/pubmed/32843078
http://dx.doi.org/10.1186/s12964-020-00631-9
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