The tau protein was critical for researchers because they wanted to understand what the protein could reveal about the mechanism behind plaques and tangles, two critical indicators doctors look for when diagnosing people with Alzheimer’s. By analyzing donated brain samples, researchers found that those with brain buildup, like plaques and tangles, but had no dementia had a normal form of tau. However, those who had a “different-handed” form of tau and developed plaques or tangles did have dementia.
You can read more about the study here.
Most proteins only survive for less than
48 hours in the body, and if they hang around too long, certain amino
acids can convert into the other-handed isomer. So that means a
left-handed isomer could inadvertently convert into a right-handed
isomer, which can lead to serious problems.
However, the human body has a solution through a process called autophagy, which clears spent or defective proteins from cells. Unfortunately, as people age autophagy slows down, especially in people over the age of 65. It’s not clear exactly why.
There are drugs currently being tested to improve the process of autophagy, and some existing ones that are approved for cardiovascular disease and other conditions could speed up the approval process. Ryan Julian, a chemistry professor at UC-Riverside involved in the research, says that “if a slowdown in autophagy is the underlying cause, things that increase it should have the beneficial, opposite effect.”
Could this be the key to unlocking a cure? It is too soon to know but this latest advance seems especially promising.
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