日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細


公開

学術論文

Vesicle condensation induced by synapsin: condensate size, geometry, and vesicle shape deformations

MPS-Authors

Taskina,  A.
Emeritus Group Laboratory of Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

/persons/resource/persons183421

Ganzella,  Marcelo
Emeritus Group Laboratory of Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

Zwicker,  D.
Emeritus Group Laboratory of Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

/persons/resource/persons15266

Jahn,  Reinhard       
Emeritus Group Laboratory of Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

External Resource
There are no locators available
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
フルテキスト (公開)

s10189-023-00404-5.pdf
(出版社版), 6MB

付随資料 (公開)
There is no public supplementary material available
引用

Alfken, J., Neuhaus, C., Major, A., Taskina, A., Hoffmann, C., Ganzella, M., Petrovic, A., Zwicker, D., Fernández-Busnadiego, R., Jahn, R., Milovanovic, D., & Salditt, T. (2024). Vesicle condensation induced by synapsin: condensate size, geometry, and vesicle shape deformations. European Physical Journal E, 47(1):. doi:10.1140/epje/s10189-023-00404-5.


引用: https://hdl.handle.net/21.11116/0000-000E-5B27-1
要旨
We study the formation of vesicle condensates induced by the protein synapsin, as a cell-free model system mimicking vesicle pool formation in the synapse. The system can be considered as an example of liquid–liquid phase separation (LLPS) in biomolecular fluids, where one phase is a complex fluid itself consisting of vesicles and a protein network. We address the pertinent question why the LLPS is self-limiting and stops at a certain size, i.e., why macroscopic phase separation is prevented. Using fluorescence light microscopy, we observe different morphologies of the condensates (aggregates) depending on the protein-to-lipid ratio. Cryogenic electron microscopy then allows us to resolve individual vesicle positions and shapes in a condensate and notably the size and geometry of adhesion zones between vesicles. We hypothesize that the membrane tension induced by already formed adhesion zones then in turn limits the capability of vesicles to bind additional vesicles, resulting in a finite condensate size. In a simple numerical toy model we show that this effect can be accounted for by redistribution of effective binding particles on the vesicle surface, accounting for the synapsin-induced adhesion zone.