A multiregional proteomic survey of the postnatal human brain.
Becky C CarlyleRobert R KitchenJean E KanyoEdward Z VossMihovil PletikosAndré M M SousaTukiet T LamMark B GersteinNenad SestanAngus C NairnPublished in: Nature neuroscience (2017)
Detailed observations of transcriptional, translational and post-translational events in the human brain are essential to improving our understanding of its development, function and vulnerability to disease. Here, we exploited label-free quantitative tandem mass-spectrometry to create an in-depth proteomic survey of regions of the postnatal human brain, ranging in age from early infancy to adulthood. Integration of protein data with existing matched whole-transcriptome sequencing (RNA-seq) from the BrainSpan project revealed varied patterns of protein-RNA relationships, with generally increased magnitudes of protein abundance differences between brain regions compared to RNA. Many of the differences amplified in protein data were reflective of cytoarchitectural and functional variation between brain regions. Comparing structurally similar cortical regions revealed significant differences in the abundances of receptor-associated and resident plasma membrane proteins that were not readily observed in the RNA expression data.
Keyphrases
- single cell
- rna seq
- label free
- tandem mass spectrometry
- binding protein
- protein protein
- electronic health record
- big data
- amino acid
- gene expression
- high resolution
- climate change
- simultaneous determination
- mass spectrometry
- high performance liquid chromatography
- white matter
- poor prognosis
- liquid chromatography
- machine learning
- multiple sclerosis
- patient safety
- solid phase extraction
- gas chromatography
- dna methylation
- ms ms
- oxidative stress
- data analysis
- functional connectivity
- deep learning
- antibiotic resistance genes
- physical activity
- weight loss
- heat shock