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The ins and outs of membrane bending by intrinsically disordered proteins
Membrane curvature is essential to diverse cellular functions. While classically attributed to structured domains, recent work illustrates that intrinsically disordered proteins are also potent drivers of membrane bending. Specifically, repulsive interactions among disordered domains drive convex be...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328403/ https://www.ncbi.nlm.nih.gov/pubmed/37418523 http://dx.doi.org/10.1126/sciadv.adg3485 |
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author | Yuan, Feng Lee, Christopher T. Sangani, Arjun Houser, Justin R. Wang, Liping Lafer, Eileen M. Rangamani, Padmini Stachowiak, Jeanne C. |
author_facet | Yuan, Feng Lee, Christopher T. Sangani, Arjun Houser, Justin R. Wang, Liping Lafer, Eileen M. Rangamani, Padmini Stachowiak, Jeanne C. |
author_sort | Yuan, Feng |
collection | PubMed |
description | Membrane curvature is essential to diverse cellular functions. While classically attributed to structured domains, recent work illustrates that intrinsically disordered proteins are also potent drivers of membrane bending. Specifically, repulsive interactions among disordered domains drive convex bending, while attractive interactions drive concave bending, creating membrane-bound, liquid-like condensates. How might disordered domains that contain both repulsive and attractive domains affect curvature? Here, we examined chimeras that combined attractive and repulsive interactions. When the attractive domain was closer to the membrane, its condensation amplified steric pressure among repulsive domains, leading to convex curvature. In contrast, when the repulsive domain was closer to the membrane, attractive interactions dominated, resulting in concave curvature. Further, a transition from convex to concave curvature occurred with increasing ionic strength, which reduced repulsion while enhancing condensation. In agreement with a simple mechanical model, these results illustrate a set of design rules for membrane bending by disordered proteins. |
format | Online Article Text |
id | pubmed-10328403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103284032023-07-08 The ins and outs of membrane bending by intrinsically disordered proteins Yuan, Feng Lee, Christopher T. Sangani, Arjun Houser, Justin R. Wang, Liping Lafer, Eileen M. Rangamani, Padmini Stachowiak, Jeanne C. Sci Adv Biomedicine and Life Sciences Membrane curvature is essential to diverse cellular functions. While classically attributed to structured domains, recent work illustrates that intrinsically disordered proteins are also potent drivers of membrane bending. Specifically, repulsive interactions among disordered domains drive convex bending, while attractive interactions drive concave bending, creating membrane-bound, liquid-like condensates. How might disordered domains that contain both repulsive and attractive domains affect curvature? Here, we examined chimeras that combined attractive and repulsive interactions. When the attractive domain was closer to the membrane, its condensation amplified steric pressure among repulsive domains, leading to convex curvature. In contrast, when the repulsive domain was closer to the membrane, attractive interactions dominated, resulting in concave curvature. Further, a transition from convex to concave curvature occurred with increasing ionic strength, which reduced repulsion while enhancing condensation. In agreement with a simple mechanical model, these results illustrate a set of design rules for membrane bending by disordered proteins. American Association for the Advancement of Science 2023-07-07 /pmc/articles/PMC10328403/ /pubmed/37418523 http://dx.doi.org/10.1126/sciadv.adg3485 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Yuan, Feng Lee, Christopher T. Sangani, Arjun Houser, Justin R. Wang, Liping Lafer, Eileen M. Rangamani, Padmini Stachowiak, Jeanne C. The ins and outs of membrane bending by intrinsically disordered proteins |
title | The ins and outs of membrane bending by intrinsically disordered proteins |
title_full | The ins and outs of membrane bending by intrinsically disordered proteins |
title_fullStr | The ins and outs of membrane bending by intrinsically disordered proteins |
title_full_unstemmed | The ins and outs of membrane bending by intrinsically disordered proteins |
title_short | The ins and outs of membrane bending by intrinsically disordered proteins |
title_sort | ins and outs of membrane bending by intrinsically disordered proteins |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328403/ https://www.ncbi.nlm.nih.gov/pubmed/37418523 http://dx.doi.org/10.1126/sciadv.adg3485 |
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