New simulations by scientists tell a tale of two taus and how they relate to neurological disease.
Their work suggests tau proteins take either of two paths to form aggregates suspected of promoting, and perhaps causing, Alzheimer's and Pick's (aka frontotemporal dementia) diseases. Precisely why remains a mystery, but figuring it out offers the possibility of controlling their fates.
Tau proteins, particularly in neurons, primarily regulate microtubules, the filaments that serve as roadways for cargo inside a cell and facilitate division. But they come in many forms and, as it turns out, these can aggregate in distinct ways.
The study in the Proceedings of the National Academy of Sciences is the first computational analysis to draw a distinction between proteins that form either the solid fibrils found in the brains of patients with Alzheimer's and Pick's or disordered, tumbleweed-like clumps that float in the neurons' cytoplasm.
"There's a relationship between the form that turns into membraneless organelles (the tumbleweeds) and the form that becomes fibers," said the senior author. "There seems to be two distinct pathways that the same tau molecule can follow, and the balance between the two pathways is affected by some biological process."
The models suggest that phosphorylation, which regulates many cellular signaling processes, may be the determining factor.
"Once we figure out which of these aggregates is the actual bad guy, then it should be possible to intervene in, say, the phosphorylation process itself in order to change the balance," the author said.
The lab used its coarse-grained AWSEM (associative memory, water-mediated, structure and energy model) analysis tool, which predicts how proteins fold, on a variety of tau protein models based on variants from patients. They found that the formation of fibers can be manipulated by phosphorylation which occurs at a multitude of sites in the tau protein.
"We found phosphorylation encouraged the formation of the amorphous aggregate, but it didn't encourage the formation of the fiber -- by as much, anyway," the author said.
Phosphorylation can also go off the rails, the author said. "There are something like 20 sites along the tau protein that can be phosphorylated, but in general, only four or five of them are," the author said. "But sometimes, they've become hyperphosphorylated, which means the enzymes responsible for the process do more. They end up with, say, 10 sites phosphorylated instead of five, and that may have some effect.
"If the extra phosphorylation can cause more of the disease, we would want to find out which kinases do the phosphorylation and try to inhibit them with a drug, like we do in treatment for cancer," the author said.
Tau proteins exhibited another interesting characteristic called backtracking, which the researchers saw in amyloid beta peptides that are also implicated in Alzheimer's. Both tend to aggregate until energetic barriers force them to partially unfold and then seek another path to their final, most stable forms.
It's at that point of frustration that aggregating taus appear to branch into different directions, the author said. One set of tau forms parallel fibrils that aggregate into the ordered plaques observed in patients' brains, while the other loosely aggregates into the floating clump. The researchers suggested the backtracking mechanism may be a universal feature in protein aggregation, a topic for future study.
The loose aggregates present their own challenges to scientists, the author said.
"They're a physics question in the following sense: They're localized objects, but why don't they all just glom together and form one huge organelle, like what happens with drops of oil in water?" he said. "Is it just that it takes too long for them to move around? Is it that they're constantly being made and disassembled? And what determines their size?
"At this point, it's still a very basic and fairly simple story," the author said. "The actual story of tau is still too complicated for us, but what we have learned so far is fairly straightforward."
What determines the tumbleweeds or fibrillar structure of Tau proteins?
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