Proteomics

Dataset Information

0

Proteomics Characterization of Longitudinal CSF from ALS Fast and Slow Progressors


ABSTRACT: Each CSF sample was concentrated and added to a multiple affinity removal spin cartridge .The eluates were subjected to a buffer exchange and proteins were reduced using DTT and alkylated using iodoacetamide. Digestions were performed using trypsin. CSF from patients with amyotrophic lateral sclerosis (ALS) was characterized via LC-MS/MS. Biomarkers were identified to differentiate fast and slow progressors.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cerebrospinal Fluid

DISEASE(S): Amyotrophic Lateral Sclerosis

SUBMITTER: Krystine Mansfield  

LAB HEAD: Patrick Pirrotte

PROVIDER: PXD035026 | Pride | 2024-01-26

REPOSITORIES: Pride

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Publications

Proteomics and mathematical modeling of longitudinal CSF differentiates fast versus slow ALS progression.

Vu Lucas L   Garcia-Mansfield Krystine K   Pompeiano Antonio A   An Jiyan J   David-Dirgo Victoria V   Sharma Ritin R   Venugopal Vinisha V   Halait Harkeerat H   Marcucci Guido G   Kuo Ya-Huei YH   Uechi Lisa L   Rockne Russell C RC   Pirrotte Patrick P   Bowser Robert R  

Annals of clinical and translational neurology 20230830 11


<h4>Objective</h4>Amyotrophic lateral sclerosis (ALS) is a heterogeneous disease with a complex etiology that lacks biomarkers predicting disease progression. The objective of this study was to use longitudinal cerebrospinal fluid (CSF) samples to identify biomarkers that distinguish fast progression (FP) from slow progression (SP) and assess their temporal response.<h4>Methods</h4>We utilized mass spectrometry (MS)-based proteomics to identify candidate biomarkers using longitudinal CSF from a  ...[more]

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