Proteomics analysis of plasma for potential biomarkers in the diagnosis of Alzheimer's disease

被引:49
作者
Liao, Pao-Chi
Yu, Lung
Kuo, Chih-Chieh
Lin, Chingju
Kuo, Yu-Min
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Cell Biol & Anat, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Inst Behav Med, Tainan 70101, Taiwan
[3] China Med Univ, Dept Physiol, Taichung, Taiwan
[4] Natl Cheng Kung Univ, Dept Environm & Occupat Hlth, Tainan 70101, Taiwan
关键词
2-DE; Alzheimer's disease; biomarkers; mass spectrometry;
D O I
10.1002/prca.200600684
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The objective of this study was to search for biological markers associated with Alzheimer's disease (AD). Plasma specimens obtained from ten pathologically diagnosed AD patients and ten non-demented (ND) control subjects were analyzed by a combination of 2-DE and MS. This strategy allowed us to identify six plasma proteins (alpha- 1-antitrypsin, vitamin D-binding protein, inter-alpha-trypsin inhibitor family heavy chain-related protein, apolipoprotein J precursor, cAMP-dependent protein kinase catalytic subunit alpha 1, and an orf) whose 2-DE spot densities were different between the AD and ND groups. Due to their involvements in AD amyloid plaque formation, the plasma concentrations of alpha- 1-antitrypsin and apolipoprotein J were further validated using either ELISA or Western blot. The results revealed that the plasma levels of alpha-1-antitrypsin in AD were higher than those of controls, confirming the 2-DE findings. However, no difference in total apolipoprotein J concentration was observed between the AD and ND groups. Considering the difference in resolving power to differentially quantitate protein isoforms provided by 2-DE and Western blot, 2-DE analysis combined with MS protein identification offers distinctive advantages when a disease-related protein isoform-specific variance is investigated.
引用
收藏
页码:506 / 512
页数:7
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