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Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis
Clathrin polymerization and changes in plasma membrane architecture are necessary steps in forming vesicles to internalize cargo during clathrin-mediated endocytosis (CME). Simultaneous analysis of clathrin dynamics and membrane structure is challenging due to the limited axial resolution of fluores...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976038/ https://www.ncbi.nlm.nih.gov/pubmed/35365614 http://dx.doi.org/10.1038/s41467-022-29317-1 |
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author | Nawara, Tomasz J. Williams, Yancey D. Rao, Tejeshwar C. Hu, Yuesong Sztul, Elizabeth Salaita, Khalid Mattheyses, Alexa L. |
author_facet | Nawara, Tomasz J. Williams, Yancey D. Rao, Tejeshwar C. Hu, Yuesong Sztul, Elizabeth Salaita, Khalid Mattheyses, Alexa L. |
author_sort | Nawara, Tomasz J. |
collection | PubMed |
description | Clathrin polymerization and changes in plasma membrane architecture are necessary steps in forming vesicles to internalize cargo during clathrin-mediated endocytosis (CME). Simultaneous analysis of clathrin dynamics and membrane structure is challenging due to the limited axial resolution of fluorescence microscopes and the heterogeneity of CME. This has fueled conflicting models of vesicle assembly and obscured the roles of flat clathrin assemblies. Here, using Simultaneous Two-wavelength Axial Ratiometry (STAR) microscopy, we bridge this critical knowledge gap by quantifying the nanoscale dynamics of clathrin-coat shape change during vesicle assembly. We find that de novo clathrin accumulations generate both flat and curved structures. High-throughput analysis reveals that the initiation of vesicle curvature does not directly correlate with clathrin accumulation. We show clathrin accumulation is preferentially simultaneous with curvature formation at shorter-lived clathrin-coated vesicles (CCVs), but favors a flat-to-curved transition at longer-lived CCVs. The broad spectrum of curvature initiation dynamics revealed by STAR microscopy supports multiple productive mechanisms of vesicle formation and advocates for the flexible model of CME. |
format | Online Article Text |
id | pubmed-8976038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89760382022-04-20 Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis Nawara, Tomasz J. Williams, Yancey D. Rao, Tejeshwar C. Hu, Yuesong Sztul, Elizabeth Salaita, Khalid Mattheyses, Alexa L. Nat Commun Article Clathrin polymerization and changes in plasma membrane architecture are necessary steps in forming vesicles to internalize cargo during clathrin-mediated endocytosis (CME). Simultaneous analysis of clathrin dynamics and membrane structure is challenging due to the limited axial resolution of fluorescence microscopes and the heterogeneity of CME. This has fueled conflicting models of vesicle assembly and obscured the roles of flat clathrin assemblies. Here, using Simultaneous Two-wavelength Axial Ratiometry (STAR) microscopy, we bridge this critical knowledge gap by quantifying the nanoscale dynamics of clathrin-coat shape change during vesicle assembly. We find that de novo clathrin accumulations generate both flat and curved structures. High-throughput analysis reveals that the initiation of vesicle curvature does not directly correlate with clathrin accumulation. We show clathrin accumulation is preferentially simultaneous with curvature formation at shorter-lived clathrin-coated vesicles (CCVs), but favors a flat-to-curved transition at longer-lived CCVs. The broad spectrum of curvature initiation dynamics revealed by STAR microscopy supports multiple productive mechanisms of vesicle formation and advocates for the flexible model of CME. Nature Publishing Group UK 2022-04-01 /pmc/articles/PMC8976038/ /pubmed/35365614 http://dx.doi.org/10.1038/s41467-022-29317-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nawara, Tomasz J. Williams, Yancey D. Rao, Tejeshwar C. Hu, Yuesong Sztul, Elizabeth Salaita, Khalid Mattheyses, Alexa L. Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title | Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title_full | Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title_fullStr | Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title_full_unstemmed | Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title_short | Imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
title_sort | imaging vesicle formation dynamics supports the flexible model of clathrin-mediated endocytosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976038/ https://www.ncbi.nlm.nih.gov/pubmed/35365614 http://dx.doi.org/10.1038/s41467-022-29317-1 |
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