TDP-43 as structure-based biomarker in amyotrophic lateral sclerosis
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
Pathologic alterations of Transactivation response DNA-binding protein 43 kilo Dalton (TDP-43) are a major hallmark of amyotrophic lateral sclerosis (ALS). In this pilot study, we analyzed the secondary structure distribution of TDP-43 in cerebrospinal fluid of ALS patients (n = 36) compared to Parkinson´s disease patients (PD; n = 30) and further controls (Ctrl; n = 24) using the immuno-infrared sensor technology. ALS patients could be discriminated from PD and Ctrl with a sensitivity/specificity of 89 %/77 % and 89 %/83 %, respectively. Our findings demonstrate that TDP-43 misfolding measured by the immuno-infrared sensor technology has the potential to serve as a biomarker candidate for ALS.
Details
| Original language | English |
|---|---|
| Pages (from-to) | 271-277 |
| Number of pages | 7 |
| Journal | Annals of clinical and translational neurology |
| Volume | 8 |
| Issue number | 1 |
| Publication status | Published - Jan 2021 |
| Peer-reviewed | Yes |
External IDs
| PubMedCentral | PMC7818221 |
|---|---|
| Scopus | 85096981048 |
Keywords
Keywords
- Aged, Amyotrophic Lateral Sclerosis/cerebrospinal fluid, Biomarkers/cerebrospinal fluid, DNA-Binding Proteins/cerebrospinal fluid, Female, Humans, Male, Middle Aged, Pilot Projects, Protein Structure, Secondary, Sensitivity and Specificity, Spectrophotometry, Infrared/methods