Aims & Methods
Aims: Advancements in biomarker development for neurodegenerative diseases, especially Alzheimer’s Disease, have accelerated with ultra-sensitive technologies like NUcleic acid-Linked Immuno-Sandwich Assay1 (NULISA) that pushes the limit of proteomic detection in low volumes of biofluids. However, detailed characterization of brain health and disease progression has been limited by the availability of comprehensive high sensitivity multiplex panels that span the broad spectrum of neurological conditions.
Methods: To interrogate a broad range of neurological diseases, we have developed new assays for key biomarkers linked to Parkinson’s disease, Ataxia, Huntington’s disease, Amyotrophic Lateral Sclerosis, Multiple Sclerosis and injury. These include post-translationally modified proteins such as pTau-205, pTau-212, and pParkin-S65, as well as disease driver mutant proteins such as mHTT and mATXN3 for the detection and monitoring of specific disease states and progression. This new panel was optimized and validated for plasma, serum and cerebrospinal fluid (CSF). Assay characteristics were assessed for precision/reproducibility, sample detectability, specificity, and dilution linearity.
