A Systematic Comparison of Alpha‐Synuclein Seed Amplification Assays for Increasing Reproducibility

Seed amplification assays (SAAs) enable ultrasensitive detection of misfolded α-synuclein across biofluids and tissues. Yet, heterogeneity in protocols limits cross-study comparability and clinical translation. Here, we review α-synuclein SAA methods and their performance across various biological matrices. We catalog key variables (e.g., human recombinant α-synuclein variants, buffers, salts, beads, shaking, incubation temperature) and outline pre-analytical factors that shape outcomes. We propose a prioritized framework of key analytical and pre-analytical variables most likely to influence assay reproducibility and clinical interpretation. We also outline minimal reporting criteria and practical quality-control checkpoints, and recommend multicenter interlaboratory proficiency testing as essential steps to accelerate the robust clinical and research implementation of α-synuclein SAAs.

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Publication Details

Journal
Annals of Clinical and Translational Neurology
Published
2026-04-01
DOI
https://doi.org/10.1002/acn3.70384
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

A Systematic Comparison of Alpha‐Synuclein Seed Amplification Assays for Increasing Reproducibility

Daniela F. Santos, Dra Tuane C R G Vieira, Tiago F. Outeiro, Manuela Amaral‐do‐Nascimento
Annals of Clinical and Translational Neurology
Parkinson's Disease Mechanisms and Treatments
article

A Systematic Comparison of Alpha‐Synuclein Seed Amplification Assays for Increasing Reproducibility

Daniela F. Santos, Dra Tuane C R G Vieira, Tiago F. Outeiro, Manuela Amaral‐do‐Nascimento
article en

Abstract

Seed amplification assays (SAAs) enable ultrasensitive detection of misfolded α-synuclein across biofluids and tissues. Yet, heterogeneity in protocols limits cross-study comparability and clinical translation. Here, we review α-synuclein SAA methods and their performance across various biological matrices. We catalog key variables (e.g., human recombinant α-synuclein variants, buffers, salts, beads, shaking, incubation temperature) and outline pre-analytical factors that shape outcomes. We propose a prioritized framework of key analytical and pre-analytical variables most likely to influence assay reproducibility and clinical interpretation. We also outline minimal reporting criteria and practical quality-control checkpoints, and recommend multicenter interlaboratory proficiency testing as essential steps to accelerate the robust clinical and research implementation of α-synuclein SAAs.

Annals of Clinical and Translational Neurology
German Center for Neurodegenerative Diseases (DE), Universitätsmedizin Göttingen (DE), Algarve Biomedical Center (PT), National Institute of Science and Technology for Structural Biology and Bioimaging (BR), Max Planck Institute for Multidisciplinary Sciences (DE), University of Algarve (PT), Newcastle University (GB)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico
Openalex Percentile: Top 30%
Parkinson's Disease Mechanisms and Treatments
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