Bottom-Up In Vitro Methods to Assay the Ultrastructural Organization, Membrane Reshaping, and Curvature Sensitivity Behavior of Septins.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
17 08 2022
Historique:
entrez: 5 9 2022
pubmed: 6 9 2022
medline: 9 9 2022
Statut: epublish

Résumé

Membrane remodeling occurs constantly at the plasma membrane and within cellular organelles. To fully dissect the role of the environment (ionic conditions, protein and lipid compositions, membrane curvature) and the different partners associated with specific membrane reshaping processes, we undertake in vitro bottom-up approaches. In recent years, there has been keen interest in revealing the role of septin proteins associated with major diseases. Septins are essential and ubiquitous cytoskeletal proteins that interact with the plasma membrane. They are implicated in cell division, cell motility, neuro-morphogenesis, and spermiogenesis, among other functions. It is, therefore, important to understand how septins interact and organize at membranes to subsequently induce membrane deformations and how they can be sensitive to specific membrane curvatures. This article aims to decipher the interplay between the ultra-structure of septins at a molecular level and the membrane remodeling occurring at a micron scale. To this end, budding yeast, and mammalian septin complexes were recombinantly expressed and purified. A combination of in vitro assays was then used to analyze the self-assembly of septins at the membrane. Supported lipid bilayers (SLBs), giant unilamellar vesicles (GUVs), large unilamellar vesicles (LUVs), and wavy substrates were used to study the interplay between septin self-assembly, membrane reshaping, and membrane curvature.

Identifiants

pubmed: 36063014
doi: 10.3791/63889
doi:

Substances chimiques

Lipid Bilayers 0
Unilamellar Liposomes 0
Septins EC 3.6.1.-

Types de publication

Journal Article Video-Audio Media Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Brieuc Chauvin (B)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université.

Koyomi Nakazawa (K)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université.

Alexandre Beber (A)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université; Institute of Biotechnology, Czech Academy of Sciences, BIOCEV.

Aurélie Di Cicco (A)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université.

Bassam Hajj (B)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université.

François Iv (F)

Institut Fresnel, CNRS UMR7249, Aix Marseille Univ, Centrale Marseille.

Manos Mavrakis (M)

Institut Fresnel, CNRS UMR7249, Aix Marseille Univ, Centrale Marseille.

Gijsje H Koenderink (GH)

Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology.

João T Cabral (JT)

Department of Chemical Engineering, Imperial College London.

Michaël Trichet (M)

Sorbonne Université, CNRS, Institut de Biologie Paris-Seine (IBPS), Service de microscopie électronique (IBPS-SME).

Stéphanie Mangenot (S)

Laboratoire Matière et Systèmes Complexes (MSC), Université Paris Cité; stephanie.mangenot@parisdescartes.fr.

Aurélie Bertin (A)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, Sorbonne Université; Aurelie.Bertin@curie.fr.

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Classifications MeSH