In the development of Parkinson’s disease (PD), the changes that will lead to neurodegeneration take place in the brain long before patients show any symptoms. But without a test that can detect these changes, it’s difficult to intervene early to more effectively slow disease progression.
To address this need, researchers have developed a molecular assay platform that they successfully applied to patient samples to detect and quantify single ⍺-synuclein fibrils, the pathogenic aggregates of ⍺-synuclein that are a hallmark of PD and other neurodegenerative disorders collectively known as ⍺-synucleinopathies. Their results are published in PNAS.
“This work is an important step toward our goal to develop a method to detect and quantify a key marker of Parkinson’s disease to help clinicians identify patients much earlier, and thus keep PD and related neurodegenerative disorders much more effectively at bay,” said corresponding author. “Having a biomarker that we can quantify could help us identify new drug candidates, and test their effects in more targeted patient cohorts at early stages of the diseases.”
Worldwide, more than 10 million people are suffering from PD, whose incidence increases with age in societies where average life expectancies have also been increasing in recent decades. In the U.S. alone, nearly 90,000 people are diagnosed with PD each year. To date, doctors must rely on neurological examination and patients’ medical histories when diagnosing PD. However, by the time clinical symptoms appear, the disease has already wreaked irreversible damage in the brain. Currently, there are no blood or laboratory tests to diagnose PD in patients lacking a known genetic predisposition, which account for about 90% of patients with PD.
PD together with multiple system atrophy (MSA) and dementia with Lewy bodies—two disorders with similarly dismal outcomes—belongs to a group of neurological disorders that have in common the pathological aggregation of the ⍺-synuclein protein into toxic fibrils. Those fibrils disrupt multiple neurological functions and ultimately cause neuronal cells to die. The neurological symptoms displayed by patients with these so-called ⍺-synucleinopathies strongly overlap, which makes it impossible to distinguish them in order to start patients on currently available therapies that are specific for each of the disorders. Importantly, none of those available therapies treats the root causes of the diseases, and they only temporarily suppress patients’ symptoms.
The researchers engineered so-called “digital seed amplification assays” (digital SAAs) that they used to detect single ⍺-synuclein fibrils in samples of brain tissue and fluid.
Using mini-compartments and immunocapture strategies, the researchers developed different diagnostic assays to detect ⍺-synuclein fibrils in patient samples. In the dSAAs, individual fibrils are separated into different types of engineered microcompartments, and then, as seeds, grown into larger fluorescent aggregates that become easily detectible and countable.
“Our digital SAAs present a critical technological advance with the potential to turn pathological ⍺-synuclein into an early biomarker for this class of neurodegenerative diseases,” said co-first author. “But work remains to be done. Our current strategies worked well on brain tissue samples from PD and MSA patients, but there’s room to improve their sensitivities so that we can meet the criteria for clinical diagnostic testing, and, hopefully, detect ⍺-synuclein fibrils in blood and other biological fluids.”
In addition to continuing to optimize the assays for diagnostic applications that, in the future, could distinguish between different ⍺-synuclein fibril structures that form in patients suffering from PD, MSA, and dementia with Lewy bodies, the team is also exploring the platforms’ potential for drug screening. They showed that the potential of a small molecule inhibitor of ⍺-synuclein aggregation can be accurately quantified using digital SAA and that the assay can read out different fibril morphologies.
“Applying the assays as a drug discovery tool could facilitate the search for promising drug candidates that more efficiently inhibit fibril formation, or even help us identify new drug targets that enable or stimulate ⍺-synuclein aggregation in the body,” said the other co-first author. “Using this system flexibly could help us better understand how we can constrain aggregate growth.”
https://www.pnas.org/doi/10.1073/pnas.2312031121
Quantification of α-synuclein aggregates
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