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How do protein tangles get so long in Alzheimer's?

Biophysicists uncover new mechanism for growth of aggregates

American Society for Biochemistry and Molecular Biology

Early in the course of Alzheimer's disease--long before future patients begin to notice symptoms--neurofibrillary tangles composed of tau protein aggregates begin to form in their brain cells. How toxic these aggregates are and how well they spread depend on their size. However, scientists studying tangle formation have not been able to explain why different sizes of cable-like tau aggregates appear in disease.

But now, researchers at The Ohio State University have discovered that instead of adding just one protein at a time, fibrils of various lengths can join end-to-end to create one longer filament. The finding, which will appear in the Journal of Biological Chemistry on Monday, helps explain how fibrils can grow to hundreds of nanometers and could also help researchers understand mechanisms of an emerging group of drug candidates designed to inhibit tau aggregation.

Scientists can use mathematical models to describe biological processes such as fibril formation. A common simple model of tau aggregation includes two steps. In the first step, two tau proteins bind slowly, and, in the second step, additional tau molecules latch on quickly.

First author Carol Huseby, a graduate student in the lab of Jeff Kuret, working in collaboration with Ralf Bundschuh, set out to expand this mathematical model to include other known ways that tau fibrils behave. Scientists have observed, for example, that sometimes one fibril fragments into two. Other times, a new fibril can nucleate in the middle of an existing fibril.

The simple two-step model predicted that a test tube filled with purified tau protein would result in a large number of short fibrils. But Huseby knew that when researchers look at aggregated tau protein under a microscope, they see a smaller number of long fibrils. That discrepancy suggested that something was happening in the real world that hadn't been accounted for in the model. They hypothesized that perhaps short fibrils could attach end-to-end to get longer.

Huseby ran a series of experiments to test the hypothesis. In one, first she labeled tau proteins with three different fluorescent colors and allowed them to aggregate in separate test tubes. Then she mixed these different colored fibrils together in a fourth test tube.

Images taken with a super-resolution fluorescence microscope showed long fibrils with short sections of each color, indicating that fibrils from original test tubes must have joined ends to form longer fibrils. Control experiments established that this can't be explained by labeled molecules' preference for like labels.

After Huseby incorporated this new mechanism into the model, it produced a much better description of what purified tau proteins were really doing as they formed aggregates. This study is the first to show that the fibrils can elongate by more than a single tau protein at a time.

Alzheimer's researchers are still trying to discern whether tau fibrils are a cause or simply an effect of the disease. One possibility is that transmission of fibrils from one cell to another may contribute to the spread of disease in the brain. A very long fibril, according to Kuret, is unlikely to spread in this way. "But once it's broken up into little pieces, those can diffuse, facilitating their movement from cell to cell."

This study used just one type of tau. Six isoforms of different length are known, and phosphorylation and other changes increase the protein's complexity. The researchers plan to incorporate these variables in future work, and to begin to use the model to understand how tau inhibitors change the protein aggregates' behavior.


This research was funded by the National Institutes of Health.

About the Journal of Biological Chemistry:

JBC is a weekly peer-reviewed scientific journal that publishes research "motivated by biology, enabled by chemistry" across all areas of biochemistry and molecular biology. To read the latest research in JBC, visit

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