Recent advances in phosphoproteomics and application to neurological diseases

被引:32
作者
Arrington, Justine V. [1 ]
Hsu, Chuan-Chih [2 ]
Elder, Sarah G. [3 ]
Tao, W. Andy [1 ,2 ,3 ,4 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Biochem, W Lafayette, IN 47907 USA
[3] Purdue Univ, Dept Med Chem & Mol Pharmacol, W Lafayette, IN 47907 USA
[4] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47907 USA
关键词
METAL AFFINITY-CHROMATOGRAPHY; PHOSPHORYLATION-DEPENDENT UBIQUITINATION; CEREBROSPINAL-FLUID BIOMARKERS; MONITORING MASS-SPECTROMETRY; CREUTZFELDT-JAKOB-DISEASE; PARAFFIN-EMBEDDED TISSUE; PROTEIN PHOSPHATASE 2A; PHOSPHOPEPTIDE ENRICHMENT; POSTTRANSLATIONAL MODIFICATIONS; QUANTITATIVE PHOSPHOPROTEOMICS;
D O I
10.1039/c7an00985b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Phosphorylation has an incredible impact on the biological behavior of proteins, altering everything from intrinsic activity to cellular localization and complex formation. It is no surprise then that this post-translational modification has been the subject of intense study and that, with the advent of faster, more accurate instrumentation, the number of large-scale mass spectrometry-based phosphoproteomic studies has swelled over the past decade. Recent developments in sample preparation, phosphorylation enrichment, quantification, and data analysis strategies permit both targeted and ultra-deep phosphoproteome profiling, but challenges remain in pinpointing biologically relevant phosphorylation events. We describe here technological advances that have facilitated phosphoproteomic analysis of cells, tissues, and biofluids and note applications to neuropathologies in which the phosphorylation machinery may be dysregulated, much as it is in cancer.
引用
收藏
页码:4373 / 4387
页数:15
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