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Advances in Proteomics Allow Insights Into Neuronal Proteomes

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Specialty Molecular Biology
Date 2021 May 3
PMID 33935646
Citations 9
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Abstract

Protein-protein interaction networks and signaling complexes are essential for normal brain function and are often dysregulated in neurological disorders. Nevertheless, unraveling neuron- and synapse-specific proteins interaction networks has remained a technical challenge. New techniques, however, have allowed for high-resolution and high-throughput analyses, enabling quantification and characterization of various neuronal protein populations. Over the last decade, mass spectrometry (MS) has surfaced as the primary method for analyzing multiple protein samples in tandem, allowing for the precise quantification of proteomic data. Moreover, the development of sophisticated protein-labeling techniques has given MS a high temporal and spatial resolution, facilitating the analysis of various neuronal substructures, cell types, and subcellular compartments. Recent studies have leveraged these novel techniques to reveal the proteomic underpinnings of well-characterized neuronal processes, such as axon guidance, long-term potentiation, and homeostatic plasticity. Translational MS studies have facilitated a better understanding of complex neurological disorders, such as Alzheimer's disease (AD), Schizophrenia (SCZ), and Autism Spectrum Disorder (ASD). Proteomic investigation of these diseases has not only given researchers new insight into disease mechanisms but has also been used to validate disease models and identify new targets for research.

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References
1.
Li J, Wilkinson B, Clementel V, Hou J, ODell T, Coba M . Long-term potentiation modulates synaptic phosphorylation networks and reshapes the structure of the postsynaptic interactome. Sci Signal. 2016; 9(440):rs8. DOI: 10.1126/scisignal.aaf6716. View

2.
Tandon R, Keshavan M, Nasrallah H . Schizophrenia, "just the facts" what we know in 2008. 2. Epidemiology and etiology. Schizophr Res. 2008; 102(1-3):1-18. DOI: 10.1016/j.schres.2008.04.011. View

3.
Rosato M, Stringer S, Gebuis T, Paliukhovich I, Li K, Posthuma D . Combined cellomics and proteomics analysis reveals shared neuronal morphology and molecular pathway phenotypes for multiple schizophrenia risk genes. Mol Psychiatry. 2019; 26(3):784-799. PMC: 7910218. DOI: 10.1038/s41380-019-0436-y. View

4.
Moutal A, White K, Chefdeville A, Laufmann R, Vitiello P, Feinstein D . Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological Functions. Mol Neurobiol. 2019; 56(10):6736-6755. PMC: 6728212. DOI: 10.1007/s12035-019-1568-4. View

5.
Kahn R, Sommer I, Murray R, Meyer-Lindenberg A, Weinberger D, Cannon T . Schizophrenia. Nat Rev Dis Primers. 2016; 1:15067. DOI: 10.1038/nrdp.2015.67. View