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Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components
FGF2 is secreted from cells by an unconventional secretory pathway. This process is mediated by direct translocation across the plasma membrane. Here, we define the minimal molecular machinery required for FGF2 membrane translocation in a fully reconstituted inside-out vesicle system. FGF2 membrane...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601999/ https://www.ncbi.nlm.nih.gov/pubmed/28722655 http://dx.doi.org/10.7554/eLife.28985 |
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author | Steringer, Julia P Lange, Sascha Čujová, Sabína Šachl, Radek Poojari, Chetan Lolicato, Fabio Beutel, Oliver Müller, Hans-Michael Unger, Sebastian Coskun, Ünal Honigmann, Alf Vattulainen, Ilpo Hof, Martin Freund, Christian Nickel, Walter |
author_facet | Steringer, Julia P Lange, Sascha Čujová, Sabína Šachl, Radek Poojari, Chetan Lolicato, Fabio Beutel, Oliver Müller, Hans-Michael Unger, Sebastian Coskun, Ünal Honigmann, Alf Vattulainen, Ilpo Hof, Martin Freund, Christian Nickel, Walter |
author_sort | Steringer, Julia P |
collection | PubMed |
description | FGF2 is secreted from cells by an unconventional secretory pathway. This process is mediated by direct translocation across the plasma membrane. Here, we define the minimal molecular machinery required for FGF2 membrane translocation in a fully reconstituted inside-out vesicle system. FGF2 membrane translocation is thermodynamically driven by PI(4,5)P(2)-induced membrane insertion of FGF2 oligomers. The latter serve as dynamic translocation intermediates of FGF2 with a subunit number in the range of 8-12 FGF2 molecules. Vectorial translocation of FGF2 across the membrane is governed by sequential and mutually exclusive interactions with PI(4,5)P(2) and heparan sulfates on opposing sides of the membrane. Based on atomistic molecular dynamics simulations, we propose a mechanism that drives PI(4,5)P(2) dependent oligomerization of FGF2. Our combined findings establish a novel type of self-sustained protein translocation across membranes revealing the molecular basis of the unconventional secretory pathway of FGF2. DOI: http://dx.doi.org/10.7554/eLife.28985.001 |
format | Online Article Text |
id | pubmed-5601999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56019992017-09-19 Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components Steringer, Julia P Lange, Sascha Čujová, Sabína Šachl, Radek Poojari, Chetan Lolicato, Fabio Beutel, Oliver Müller, Hans-Michael Unger, Sebastian Coskun, Ünal Honigmann, Alf Vattulainen, Ilpo Hof, Martin Freund, Christian Nickel, Walter eLife Biochemistry FGF2 is secreted from cells by an unconventional secretory pathway. This process is mediated by direct translocation across the plasma membrane. Here, we define the minimal molecular machinery required for FGF2 membrane translocation in a fully reconstituted inside-out vesicle system. FGF2 membrane translocation is thermodynamically driven by PI(4,5)P(2)-induced membrane insertion of FGF2 oligomers. The latter serve as dynamic translocation intermediates of FGF2 with a subunit number in the range of 8-12 FGF2 molecules. Vectorial translocation of FGF2 across the membrane is governed by sequential and mutually exclusive interactions with PI(4,5)P(2) and heparan sulfates on opposing sides of the membrane. Based on atomistic molecular dynamics simulations, we propose a mechanism that drives PI(4,5)P(2) dependent oligomerization of FGF2. Our combined findings establish a novel type of self-sustained protein translocation across membranes revealing the molecular basis of the unconventional secretory pathway of FGF2. DOI: http://dx.doi.org/10.7554/eLife.28985.001 eLife Sciences Publications, Ltd 2017-07-19 /pmc/articles/PMC5601999/ /pubmed/28722655 http://dx.doi.org/10.7554/eLife.28985 Text en © 2017, Steringer et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Steringer, Julia P Lange, Sascha Čujová, Sabína Šachl, Radek Poojari, Chetan Lolicato, Fabio Beutel, Oliver Müller, Hans-Michael Unger, Sebastian Coskun, Ünal Honigmann, Alf Vattulainen, Ilpo Hof, Martin Freund, Christian Nickel, Walter Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title | Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title_full | Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title_fullStr | Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title_full_unstemmed | Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title_short | Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
title_sort | key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601999/ https://www.ncbi.nlm.nih.gov/pubmed/28722655 http://dx.doi.org/10.7554/eLife.28985 |
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