期刊
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
卷 -, 期 185, 页码 -出版社
JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/64090
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资金
- National Institutes of Health (NIH) [R01 GM-130934]
- National Science Foundation (NSF) [MCB-2016022]
- National Institute of General Medical Sciences [T32 GM119999]
Most cells can sense and change their shape to carry out cell processes, with the septin cytoskeleton playing a vital role in coordinating shape changes. Septins assemble into higher-order structures and are found in regions of positive curvature on the cell membrane. Reconstituting the septin cytoskeleton in a cell-free system has allowed for the study of assembly mechanisms at high resolution. Understanding how septins assemble and sense curvature at different stages is crucial for understanding cell shape changes.
Most cells can sense and change their shape to carry out fundamental cell processes. In many eukaryotes, the septin cytoskeleton is an integral component in coordinating shape changes like cytokinesis, polarized growth, and migration. Septins are filament-forming proteins that assemble to form diverse higher-order structures and, in many cases, are found in different areas of the plasma membrane, most notably in regions of micron-scale positive curvature. Monitoring the process of septin assembly in vivo is hindered by the limitations of light microscopy in cells, as well as the complexity of interactions with both membranes and cytoskeletal elements, making it difficult to quantify septin dynamics in living systems. Fortunately, there has been substantial progress in the past decade in reconstituting the septin cytoskeleton in a cell-free system to dissect the mechanisms controlling septin assembly at high spatial and temporal resolutions. The core steps of septin assembly include septin heterooligomer association and dissociation with the membrane, polymerization into filaments, and the formation of higher-order structures through interactions between filaments. Here, we present three methods to observe septin assembly in different contexts: planar bilayers, spherical supports, and rod supports. These methods can be used to determine the biophysical parameters of septins at different stages of assembly: as single octamers binding the membrane, as filaments, and as assemblies of filaments. We use these parameters paired with measurements of curvature sampling and preferential adsorption to understand how curvature sensing operates at a variety of length and time scales.
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