Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
_version_ 1783264502631890944
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
work_keys_str_mv AT steringerjuliap keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT langesascha keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT cujovasabina keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT sachlradek keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT poojarichetan keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT lolicatofabio keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT beuteloliver keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT mullerhansmichael keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT ungersebastian keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT coskununal keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT honigmannalf keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT vattulainenilpo keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT hofmartin keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT freundchristian keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents
AT nickelwalter keystepsinunconventionalsecretionoffibroblastgrowthfactor2reconstitutedwithpurifiedcomponents