Understanding healthy function of tau, protein associated with dementia
Tau protein is implicated in a wide range of neurodegenerative diseases, said Kassandra Ori-McKenney, associate professor in the UC Davis Department of Molecular and Cellular Biology and a corresponding author on the paper. The brains of people with Alzheimer’s disease contain tangles of tau protein and plaques of another protein, beta amyloid. However, tau protein tangles also occur in a variety of diseases, collectively referred to as “tauopathies,” and other neurodegenerative conditions, including following traumatic brain injury.
It was thought that “healthy” tau exists as single protein molecules, and that tau causes disease when it clumps together with other tau proteins, forming the insoluble tau tangles. But in 2019, Ori-McKenney and Richard McKenney, associate professor in the same department, showed that healthy tau could self-associate and come apart again, revealing that self-association of tau molecules may not necessarily always lead to pathology.
“In its natural form tau can self-assemble and disassemble, so what is the tipping point that produces a form where it can’t disassemble and forms a tangle?” Ori-McKenney said.
Tau associated with microtubules
Tau is one of a group of proteins found in all kinds of cells, from single cell amoebas to insects to people, that associate with microtubules, large protein filaments that fill the inside of cells. Microtubules provide a framework within the cell that provides structure and organization, as well as allowing items to move around within the cell and for the cell itself to move. For these things to happen, microtubules have to interact with many other proteins.
Their 2019 paper showed that healthy tau molecules could assemble with each other, forming an “envelope” around microtubules, a novel behavior that the authors showed could play a regulatory role by making it harder, or easier, for certain other proteins to attach to the microtubule.
In the new paper, Ori-McKenney, McKenney and collaborators in the Czech Republic carried out a series of experiments with tau proteins and isolated microtubules. They found that not only can tau self-assemble to form an envelope around microtubules, but that when it does so it squeezes the microtubule into a more compact form. It can do this because microtubules are made up of pairs (dimers) of individual tubulin proteins, and there is a little bit of squishiness — about two angstroms — between dimers.
This means that tau protein can change the compaction along a length of microtubule, which in turn affects how other proteins attach to it. For example, kinesin-1, a motor protein that can move along microtubules, will only attach to an expanded microtubule.
The team also looked at other proteins that are evolutionarily related to tau, microtubule associated proteins (MAP) 2 and 4. MAP2, they found, behaves like tau and can compact microtubules but MAP4 does not. These results suggest that tau and MAP2 might have evolved the ability to compact microtubules for specific functions within cells. Interestingly, both proteins are largely found only in the nervous system, while MAP4 is found in most tissues in the body, suggesting the roles of tau and MAP2 in microtubule compaction may be very important in neurons.
Neither MAP2 or MAP4 are known to be associated with disease states. In future work, the researchers hope to figure out the steps between healthy tau self-assembly and pathological irreversible tangles and the roles of these proteins in different organisms.
Additional authors on the paper are: at UC Davis, Ruensern Tan, Tracy Tan and Mariah Dacy; Valerie Siahaan, Marcus Braun and Zdenek Lansky, Czech Academy of Sciences, Prague; Tereza Humhalova and Lenka Libusova, Charles University, Prague; and Samuel Lacey, MRC Laboratory of Molecular Biology, Cambridge, U.K. The work was partly supported by funds from the Pew Charitable Trusts, the Czech Science Foundation, Czech Academy of Sciences and Charles University.