Neuroproteomics: Expression profiling of the brain's proteomes in health and disease

被引:96
作者
Kim, SI
Voshol, H
van Oostrum, J
Hastings, TG
Cascio, M
Glucksman, MJ
机构
[1] Finch Univ Hlth Sci Chicago Med Sch, Dept Biochem & Mol Biol, Midw Proteome Ctr, N Chicago, IL 60064 USA
[2] Novartis Inst Biomed Res, Dept Funct Genom, Basel, Switzerland
[3] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Sch Med, Dept Neurosci, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
关键词
brain; neurodegenerative; neurome; Parkinson's disease; proteome; psychiatric;
D O I
10.1023/B:NERE.0000023618.35579.7c
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The term "proteome" describes the protein complement of a genome. Proteomes of cells are dynamic and are directly affected by environmental factors, such as stress and/or drug treatment, or as a result of aging and disease. One of the distinct advantages of proteomic analysis, not attainable with RNA expression data, is the ability to fractionate the cell's proteins into various subpopulations. In neuroscience, "neuromics" (proteomics in the central nervous system) is in its infancy, with a paucity of studies in the context of the brain. One of the objectives of this review is to illustrate the potential of neuromics to profile differences in the distribution of thousands of proteins as a function of disease markers. We have previously used this approach to determine the effects of varied postmortem interval in examining human brain tissue and to identify biomarkers. Here we review proteomic studies of schizophrenia, Alzheimer's disease, and Parkinson's disease. Experimental results regarding Parkinson's disease are presented to illustrate the potential of neuromics to identify pathways of pathogenesis and novel therapeutic targets.
引用
收藏
页码:1317 / 1331
页数:15
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