In Vitro Reconstitution of Dynamic Co-organization of Microtubules and Actin Filaments in Emulsion Droplets.
Actin Cytoskeleton
/ chemistry
Actins
/ metabolism
Centrosome
/ metabolism
Cytoskeleton
/ metabolism
Data Interpretation, Statistical
Emulsions
Lipid Droplets
/ ultrastructure
Lipids
/ chemistry
Microfluidic Analytical Techniques
Microfluidics
/ instrumentation
Microtubules
/ chemistry
Protein Binding
Confinement
Cytolinkers
Cytoskeleton
In vitro reconstitution
Microtubule dynamic instability
Self-organization
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
28
12
2019
pubmed:
28
12
2019
medline:
20
1
2021
Statut:
ppublish
Résumé
In vitro (or cell-free) reconstitution is a powerful tool to study the physical basis of cytoskeletal organization in eukaryotic cells. Cytoskeletal reconstitution studies have mostly been done for individual cytoskeleton systems in unconfined 3D or quasi-2D geometries, which lack complexity relative to a cellular environment. To increase the level of complexity, we present a method to study co-organization of two cytoskeletal components, namely microtubules and actin filaments, confined in cell-sized water-in-oil emulsion droplets. We show that centrosome-nucleated dynamic microtubules can be made to interact with actin filaments through a tip-tracking complex consisting of microtubule end-binding proteins and an actin-microtubule cytolinker. In addition to the protocols themselves, we discuss the optimization steps required in order to build these more complex in vitro model systems of cytoskeletal interactions.
Identifiants
pubmed: 31879898
doi: 10.1007/978-1-0716-0219-5_5
doi:
Substances chimiques
Actins
0
Emulsions
0
Lipids
0
Types de publication
Journal Article
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM