Small "bubbles" frequently form on membranes of cells and are taken up into their interior. The process involves EHD proteins - a focus of research by Prof. Oliver Daumke of the MDC. He and his team have now shed light on how these proteins assemble on the surface of a cell and reshape its membrane.
Fairground entertainers can transform simple balloons into elaborate figures with just a few twists. They do this by "pinching off" sections of the balloon's surface - a method similar to that used by cells to create small bubbles known as vesicles for the transport of molecules. Vesicles are used to take up nutrients and play an important role in the transmission of neural signals.
EHD proteins are one type of molecular machine responsible for the creation of vesicles. These proteins bind themselves to the inside of a cell membrane, where they form long chains and ring-like structures. The rings then invaginate the membrane, contract like a drawstring, and, finally, detach the vesicle from the surface of the cell.
Oliver Daumke of the Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC) is investigating the function and spatial structure of these EHD proteins. In an earlier study, he and his team analyzed the three-dimensional structure of EHDs in an inactive form - i.e. not bound to the membrane. Until now, scientists did not know how EHD proteins become activated, attach to the membrane and shape it into tubular structures.
Together with international colleagues, Daumke and his PhD student Arthur Alves de Melo have now published an article in the current issue of the scientific journal PNAS that describes the active form of this molecular EHD machine - that which occurs when it comes into contact with the membrane. Comparing the active and inactive protein structures, they discovered that EHD molecules flip open when they bind to the membrane, exposing specialized regions. One of these regions allows them to organize in extended chains and ring-like structures. Another region reorients toward the membrane and anchors the molecular machines on the cell surface.
With this work, Daumke's team has now described two steps in the operation of EHDs. "To understand the complete operating cycle and thus the full function of these molecular EHD machines, we must now analyze various other states," he says. "That is a task for the coming years."
Arthur Alves Melo et al. (2017): "Structural insights into the activation mechanism of dynamin-like Eps15-homology domain proteins." PNAS.