PXD000666-3

PXD000666 is an original dataset announced via ProteomeXchange.

Title	Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics
Description	The fatal neurodegenerative disorders amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA) are the most common motoneuron disease and genetic cause of infant death, respectively. Various in vitro model systems have been established to investigate motoneuron disease mechanisms - in particular immortalized cell lines and primary neurons. By quantitative mass spectrometry (MS)-based proteomics we here compare the proteomes of primary motoneurons to motoneuron-like cell lines NSC-34 and N2a as well as to non-neuronal control cells at a depth of 10,000 proteins. We use this resource to evaluate the suitability of murine in vitro model systems for cell biological and biochemical analysis of motoneuron disease mechanisms. Individual protein and pathway analysis indicate substantial differences between motoneuron-like cell lines and primary motoneurons, especially for proteins involved in differentiation, cytoskeleton and receptor signaling, whereas common metabolic pathways were more similar. The ALS-associated proteins themselves also showed distinct differences between cell lines and primary motoneurons, providing a molecular basis for understanding fundamental alterations between cell lines and neurons with respect to neuronal pathways with relevance for disease mechanisms. Our study provides a proteomics resource for motoneuron research and presents a paradigm of how MS-based proteomics can be used to evaluate disease model systems
HostingRepository	PRIDE
AnnounceDate	2014-09-10
AnnouncementXML	Submission_2014-09-10_00:30:51.xml
DigitalObjectIdentifier
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Unsupported dataset by repository
PrimarySubmitter	Mario Oroshi
SpeciesList	scientific name: Mus musculus (Mouse); NCBI TaxID: 10090;
ModificationList	monohydroxylated residue; acetylated residue; iodoacetamide derivatized residue
Instrument	Q Exactive

Revision	Datetime	Status	ChangeLog Entry
0	2013-12-23 03:54:50	ID requested
1	2014-09-09 08:01:54	announced
2	2014-09-09 08:25:48	announced	Updated publication reference for PubMed record(s): 25193168.
⏵ 3	2014-09-10 00:30:52	announced	Updated project metadata.
4	2014-10-23 02:52:41	announced	Updated project metadata.
5	2024-10-22 04:18:04	announced	2024-10-22: Updated project metadata.

Hornburg D, Drepper C, Butter F, Meissner F, Sendtner M, Mann M, Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics. Mol Cell Proteomics, 13(12):3410-20(2014) [pubmed]

curator keyword: Biomedical

submitter keyword: neurodegeneration, quantitative proteomics, neuron, motoneuron, amyotrophic lateral sclerosis, ALS,

Matthias Mann
contact affiliation	Department of Proteomics and Signal Transduction Max Planck Institute of Biochemistry
contact email	mmann@biochem.mpg.de
lab head
Mario Oroshi
contact affiliation	Proteomics
contact email	oroshi@biochem.mpg.de
dataset submitter

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PRIDE project URI

• PRIDE
  1. PXD000666
     1. Label: PRIDE project
     2. Name: Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics