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Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes

S100 proteins are small, dimeric, Ca(2+)-binding proteins of considerable interest due to their associations with cancer and rheumatic and neurodegenerative diseases. They control the functions of numerous proteins by forming protein–protein complexes with them. Several of these complexes were found...

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Autores principales: Ecsédi, Péter, Gógl, Gergő, Nyitray, László
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542695/
https://www.ncbi.nlm.nih.gov/pubmed/34708078
http://dx.doi.org/10.3389/fmolb.2021.749052
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author Ecsédi, Péter
Gógl, Gergő
Nyitray, László
author_facet Ecsédi, Péter
Gógl, Gergő
Nyitray, László
author_sort Ecsédi, Péter
collection PubMed
description S100 proteins are small, dimeric, Ca(2+)-binding proteins of considerable interest due to their associations with cancer and rheumatic and neurodegenerative diseases. They control the functions of numerous proteins by forming protein–protein complexes with them. Several of these complexes were found to display “fuzzy” properties. Examining these highly flexible interactions, however, is a difficult task, especially from a structural biology point of view. Here, we summarize the available in vitro techniques that can be deployed to obtain structural information about these dynamic complexes. We also review the current state of knowledge about the structures of S100 complexes, focusing on their often-asymmetric nature.
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spelling pubmed-85426952021-10-26 Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes Ecsédi, Péter Gógl, Gergő Nyitray, László Front Mol Biosci Molecular Biosciences S100 proteins are small, dimeric, Ca(2+)-binding proteins of considerable interest due to their associations with cancer and rheumatic and neurodegenerative diseases. They control the functions of numerous proteins by forming protein–protein complexes with them. Several of these complexes were found to display “fuzzy” properties. Examining these highly flexible interactions, however, is a difficult task, especially from a structural biology point of view. Here, we summarize the available in vitro techniques that can be deployed to obtain structural information about these dynamic complexes. We also review the current state of knowledge about the structures of S100 complexes, focusing on their often-asymmetric nature. Frontiers Media S.A. 2021-10-11 /pmc/articles/PMC8542695/ /pubmed/34708078 http://dx.doi.org/10.3389/fmolb.2021.749052 Text en Copyright © 2021 Ecsédi, Gógl and Nyitray. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Ecsédi, Péter
Gógl, Gergő
Nyitray, László
Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title_full Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title_fullStr Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title_full_unstemmed Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title_short Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes
title_sort studying the structures of relaxed and fuzzy interactions: the diverse world of s100 complexes
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542695/
https://www.ncbi.nlm.nih.gov/pubmed/34708078
http://dx.doi.org/10.3389/fmolb.2021.749052
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