The proteomics of neurodegeneration

被引:22
|
作者
Johnson, MD
Yu, LR
Conrads, TP
Kinoshita, Y
Uo, T
McBee, JK
Veenstra, TD
Morrison, RS
机构
[1] Univ Washington, Sch Med, Dept Neurol Surg, Seattle, WA 98195 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02115 USA
[3] NCI, SAIC Frederick Inc, Lab Proteom & Analyt Technol, Frederick, MD USA
关键词
D O I
10.2165/00129785-200505040-00006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The continuing improvement and refinement of proteomic and bioinformatic tools has made it possible to obtain increasing amounts of structural and functional information about proteins on a global scale. The emerging field of neuroproteomics promises to provide powerful strategies for further charactenzing neuronal dysfunction and cell loss associated with neurodegenerative diseases. Neuroproteomic studies have thus far revealed relatively comprehensive quantitative changes and post-translational modifications (mostly oxidative damage) of high abundance proteins, confirming deficits in energy production, protein degradation, antioxidant protein function, and cytoskeletal regulation associated with neurodegenerative diseases such as Alzheimer and Parkinson disease. The identification of changes in low-abundance proteins and characterization of their functions based on protein-protein interactions still await further development of proteomic methodologies and more dedicated application of these technologies by neuroscientists. Once accomplished, however, the resulting information will certainly provide a truly comprehensive view of neurodegeneration-associated changes in protein expression, facilitating the identification of novel biomarkers for the early detection of neurodegenerative diseases and new targets for therapeutic intervention.
引用
收藏
页码:259 / 270
页数:12
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