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Effects of pH alterations on stress- and aging-induced protein phase separation
Upon stress challenges, proteins/RNAs undergo liquid–liquid phase separation (LLPS) to fine-tune cell physiology and metabolism to help cells adapt to adverse environments. The formation of LLPS has been recently linked with intracellular pH, and maintaining proper intracellular pH homeostasis is kn...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232405/ https://www.ncbi.nlm.nih.gov/pubmed/35750966 http://dx.doi.org/10.1007/s00018-022-04393-0 |
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author | Jin, Xuejiao Zhou, Min Chen, Shuxin Li, Danqi Cao, Xiuling Liu, Beidong |
author_facet | Jin, Xuejiao Zhou, Min Chen, Shuxin Li, Danqi Cao, Xiuling Liu, Beidong |
author_sort | Jin, Xuejiao |
collection | PubMed |
description | Upon stress challenges, proteins/RNAs undergo liquid–liquid phase separation (LLPS) to fine-tune cell physiology and metabolism to help cells adapt to adverse environments. The formation of LLPS has been recently linked with intracellular pH, and maintaining proper intracellular pH homeostasis is known to be essential for the survival of organisms. However, organisms are constantly exposed to diverse stresses, which are accompanied by alterations in the intracellular pH. Aging processes and human diseases are also intimately linked with intracellular pH alterations. In this review, we summarize stress-, aging-, and cancer-associated pH changes together with the mechanisms by which cells regulate cytosolic pH homeostasis. How critical cell components undergo LLPS in response to pH alterations is also discussed, along with the functional roles of intracellular pH fluctuation in the regulation of LLPS. Further studies investigating the interplay of pH with other stressors in LLPS regulation and identifying protein responses to different pH levels will provide an in-depth understanding of the mechanisms underlying pH-driven LLPS in cell adaptation. Moreover, deciphering aging and disease-associated pH changes that influence LLPS condensate formation could lead to a deeper understanding of the functional roles of biomolecular condensates in aging and aging-related diseases. |
format | Online Article Text |
id | pubmed-9232405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-92324052022-06-26 Effects of pH alterations on stress- and aging-induced protein phase separation Jin, Xuejiao Zhou, Min Chen, Shuxin Li, Danqi Cao, Xiuling Liu, Beidong Cell Mol Life Sci Review Upon stress challenges, proteins/RNAs undergo liquid–liquid phase separation (LLPS) to fine-tune cell physiology and metabolism to help cells adapt to adverse environments. The formation of LLPS has been recently linked with intracellular pH, and maintaining proper intracellular pH homeostasis is known to be essential for the survival of organisms. However, organisms are constantly exposed to diverse stresses, which are accompanied by alterations in the intracellular pH. Aging processes and human diseases are also intimately linked with intracellular pH alterations. In this review, we summarize stress-, aging-, and cancer-associated pH changes together with the mechanisms by which cells regulate cytosolic pH homeostasis. How critical cell components undergo LLPS in response to pH alterations is also discussed, along with the functional roles of intracellular pH fluctuation in the regulation of LLPS. Further studies investigating the interplay of pH with other stressors in LLPS regulation and identifying protein responses to different pH levels will provide an in-depth understanding of the mechanisms underlying pH-driven LLPS in cell adaptation. Moreover, deciphering aging and disease-associated pH changes that influence LLPS condensate formation could lead to a deeper understanding of the functional roles of biomolecular condensates in aging and aging-related diseases. Springer International Publishing 2022-06-24 2022 /pmc/articles/PMC9232405/ /pubmed/35750966 http://dx.doi.org/10.1007/s00018-022-04393-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Jin, Xuejiao Zhou, Min Chen, Shuxin Li, Danqi Cao, Xiuling Liu, Beidong Effects of pH alterations on stress- and aging-induced protein phase separation |
title | Effects of pH alterations on stress- and aging-induced protein phase separation |
title_full | Effects of pH alterations on stress- and aging-induced protein phase separation |
title_fullStr | Effects of pH alterations on stress- and aging-induced protein phase separation |
title_full_unstemmed | Effects of pH alterations on stress- and aging-induced protein phase separation |
title_short | Effects of pH alterations on stress- and aging-induced protein phase separation |
title_sort | effects of ph alterations on stress- and aging-induced protein phase separation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232405/ https://www.ncbi.nlm.nih.gov/pubmed/35750966 http://dx.doi.org/10.1007/s00018-022-04393-0 |
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