This ‘swallowing’, called endocytosis, is involved in a variety of crucial tasks. It is used by brain cells relaying information to each other and is also hijacked by many viruses, which use it to invade their host’s cells. When a cell is about to swallow some molecules, a dent appears in the cell’s membrane, and gradually expands inwards, pinching off to form a little pouch, or vesicle, that transports molecules into the cell.
To investigate how the cell’s machinery pulls in the membrane and forms the vesicle, researchers led by Marko Kaksonen and John Briggs at the European Molecular Biology Laboratory (EMBL) in Heidelberg employed a method they developed two years ago to faithfully follow the exact same molecules first under a light microscope and then with the higher resolution of an electron microscope. This enabled them to combine two sets of data that so far could only be obtained in isolation: the timing and sequence with which different components of the cell’s machinery arrive at the vesicle-to-be, and the 3D changes to membrane shape that ultimately form that vesicle.
They discovered, for instance, that the first proteins to arrive on the inside of the cell’s membrane are not able to start bending it inwards until a network of the cell’s scaffolding protein, actin, forms and starts pulling on the membrane.
The data used to make the video is freely available to the scientific community and will, Kaksonen and Briggs believe, provide valuable information to others trying to develop physical models of how this process works. They are probing the roles of individual proteins in this process, by perturbing them, and would like to extend the current work in yeast to human cells.
Citation: Kukulski, W., Schorb, M., Kaksonen, M.&Briggs, J.A.B. Time-resolved electron tomography reveals how the plasma membrane is reshaped during endocytosis. Cell, 3 August 2012.