化学学报 ›› 2009, Vol. 67 ›› Issue (2): 167-173. 上一篇    下一篇

研究论文

不稳定性心绞痛血瘀证的血浆蛋白质组学研究

赵慧辉 王 伟*

  

  1. (北京中医药大学研究生院 北京100029)
  • 投稿日期:2008-02-04 修回日期:2008-07-08 发布日期:2009-01-28
  • 通讯作者: 王伟

Plasma Proteomics Study on Unstable Angina Patients with Blood Stasis Syndrome

Zhao, Huihui Wang, Wei*   

  1. (Graduate School of Beijing University of Traditional Chinese Medicine, Beijing 100029)
  • Received:2008-02-04 Revised:2008-07-08 Published:2009-01-28
  • Contact: Wang, Wei

为了寻找冠心病不稳定性心绞痛血瘀证血浆差异表达蛋白, 探索冠心病不稳定性心绞痛血瘀证的蛋白质组学特点. 采用差异凝胶双向电泳和质谱联用技术对12例冠心病不稳定性心绞痛血瘀证患者和12例健康人血浆进行比较研究. 初步发现了Fibrinogen β chain, Fibrinogen γ chain, α1-Antitrypsin, Haptoglobin β chain, Haptoglobin α2 chain在冠心病不稳定性心绞痛血瘀证患者中高表达, ApoA-IV, ApoA-I, Transthyretin, ApoJ在冠心病不稳定性心绞痛血瘀证患者中低表达. 差异表达蛋白根据功能可分为以下三类: (1)急性时相反应负相蛋白; (2)载脂蛋白; (3)凝血相关蛋白. 冠心病不稳定性心绞痛血瘀证可能与炎症反应、脂代谢紊乱以及凝血功能异常相关.

关键词: 心绞痛, 血瘀证, 差异凝胶电泳, 蛋白质组, 生物标志物

To seek differentially expressed plasma proteins of unstable angina patients with blood stasis syndrome, two-dimensional difference gel electrophoresis and mass spectrometry were used to screen the differentially expressed plasma proteins among such patients with blood stasis syndrome and healthy volunteers. Fibrinogen β chain, fibrinogen γ chain, α1-antitrypsin, haptoglobin β chain, haptoglobin α2 chain were significantly highly expressed in the plasma of these patients, while ApoA-IV, ApoA-I, transthyretin and ApoJ were decreased in their plasma. These identified increased expressed proteins could be divided into three categories according to their functions: (1) acute phase reactive protein, (2) apolipoprotein, (3) blood coagulation protein. Unstable angina with blood stasis syndrome may be correlated with inflammatory reaction, lipid metabolic disorder and blood coagulation factor abnormality, and these differentially expressed proteins could provide clues for the study of unstable angina biomarkers and discovery of new protein targets for antianginal drugs.

Key words: unstable angina, blood stasis syndrome, difference gel electrophoresis (DIGE), proteome, biomarker