Biology subjects

Carretero-Genevrier, A.

Publications and source records attributed to Carretero-Genevrier, A..

4 recordsLinked to original sources

bioRxiv2024

Septin filament assembly assists the lateral organization of membranes

Compartmentalized interactions of plasma membrane components are essential to support many cell functions, from signaling to cell division, adhesion, migration, or phagocytosis. Cytoskeletal-membrane interactions play an important role in forming membrane compartments, and this feature has been primarily studied through the actin cytoskeleton. Unlike actin, septins directly interact with membranes, acting as scaffolds to recruit proteins to specific cellular locations and as structural diffusion barriers for membrane components. However, how septins interact with and remodel the local membrane environment is unclear. Here we combined minimal reconstituted systems based on fluorescence microscopy and quantitative atomic force microscopy together with live yeast cell imaging and STED microscopy to study septin-mediated membrane organization. Our results show that septins self-assembly into filament-based sub-micrometric patches and high-order structures prompt their membrane-organizing role in vitro and in yeast cells, respectively. Furthermore, we show that the polybasic domain of Cdc11, in addition to the amphipathic helix of Cdc12, plays an essential role in supporting the membrane remodeling and curvature-sensing properties of yeast septins. Collectively, our work provides a framework for understanding the molecular mechanisms by which septins can support cellular functions intimately linked to membranes.

cell biology↗

bioRxiv2021

Structure and dynamics of FCHo2 docking on membranes

Clathrin-mediated endocytosis (CME) is a central trafficking pathway in eukaryotic cells regulated by phosphoinositides. The plasma membrane phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) plays an instrumental role in driving CME initiation. The F-BAR domain only protein 1 and 2 complex (FCHo1/2) is among the early proteins that reach the plasma membrane, but the exact mechanisms triggering its recruitment remains elusive. Here, we show the molecular dynamics of FCHo2 self-assembly on membranes by combining bottom-up synthetic approaches on in vitro and cellular membranes. Our results indicate that PI(4,5)P2 domains assist FCHo2 docking at specific membrane regions, where it self-assembles into ring-like shape protein patches. We show that binding of FCHo2 on cellular membranes promotes PI(4,5)P2 clustering at the boundary of cargo receptors and that this accumulation enhances clathrin assembly. Thus, our results provide a mechanistic framework that could explain the recruitment of early PI(4,5)P2-interacting proteins at endocytic sites.

biophysics↗

bioRxiv2019

Nanoscale topography templates the organization of stable clathrin/AP-2 structures

Membrane shape is a key feature of many cellular processes, including cell differentiation, division, migration, and trafficking. The development of nanostructured surfaces allowing for the in situ manipulation of membranes in living cells is crucial to understand these processes, but this requires complicated and limited-access technologies. Here, we investigate the self-organization of cellular membranes by using a customizable and bench top method allowing to engineer 1D SiO2 nanopillar arrays of defined sizes and shapes on high-performance glass compatible with advanced microscopies. As a result of this original combination, we provide a mapping of the morphology-induced modulation of the cell membrane mechanics, dynamics and steady-state organization of key protein complexes implicated in cellular trafficking and signal transduction.

biophysics↗

bioRxiv2018

Quantitative Mapping of Free-Standing Lipid Membranes on Nano-Porous Mica Substrates

The physic-chemistry of biological membranes is at the origin of fundamental cellular functions such as vesicle trafficking, cell adhesion and migration1-3. Because most of intracellular shapes and local demixing of membranes take place in the nanometer scale, AFM becomes an extremely powerful technique to assess the properties of these biological membranes. Porous substrates provide an elegant strategy to avoid the conundrum of placing soft and thin biomembranes on hard substrates for AFM studies, although the surface chemistry make the actual substrates rather challenging setups. Here, we have engineered porous systems on the most widely used substrate in AFM, mica muscovite, with tunable pore sizes from some tens to few hundreds nanometers for biological applications. We show that free-standing bilayers on nano-porous can be obtained by using well-established vesicle spreading methods and that they display equivalent nano-mechanical stability and phsyco-chemical properties to that of membranes on conventional mica supports. By reducing the pore radius < 40 nm and limiting the contribution of membrane tension to the elastic response of free-standing membranes we estimate a bending modulus of 18 kbT and 73 kbT for DOPC and DPPC bilayers, respectively. The quantitative mapping of suspended membranes shows a different mechanical response at the pore rims, which is more pronounced for DPPC and suggest a different lipid ordering. We find that the combination of membrane bending and the different lipid packing at the edges of pores shapes the curvature of free-standing membranes on pores in the range of few tens of nm.

biophysics↗