首都医科大学学报 ›› 2009, Vol. 30 ›› Issue (3): 331-335.doi: 10.3785/j.issn.1006-7795.2009.03.016

• 基础研究 • 上一篇    下一篇

Hela细胞蛋白质分离和肽质量指纹谱鉴定方法的建立

胡家1, 李燕英2, 孙丽翠1,3, 殷爱红1, 武文琦1, 贺俊崎1,3   

  1. 1. 首都医科大学医学实验与测试中心;2. 北京理工大学附属医院;3. 首都医科大学生物化学与分子生物学系
  • 收稿日期:2008-10-08 修回日期:1900-01-01 出版日期:2009-06-21 发布日期:2009-06-21
  • 通讯作者: 贺俊崎

Identification of Proteins from Hela Cells by Two-Dimensional Electrophoresis and Peptide Mass Fingerprinting

HU Jia1, LI Yan-ying2, SUN Li-cui1,3, YIN Ai-hong1, WU Wen-qi1, HE Jun-qi1,3   

  1. 1. Medical Experiment and Test Center, Capital Medical University;2. Hospital of Beijing Institute of Technology;3. Department of Biochemistry and Molecular Biology, Capital Medical University
  • Received:2008-10-08 Revised:1900-01-01 Online:2009-06-21 Published:2009-06-21

摘要:

目的 研究Hela细胞总蛋白质的分离及利用肽质量指纹谱对蛋白质进行鉴定的方法。方法 提取了Hela细胞的总蛋白质,通过双向电泳技术对蛋白质进行了分离,并应用图像扫描仪及图像分析软件获取蛋白质点的数字化信息。对其中不同丰度的蛋白质点,进行胶内酶切后,通过基质辅助激光解吸/电离直角型飞行时间质谱(MALDI O-TOF-MS)分析,再将检测出的多肽质量数通过Mascot搜索引擎检索NCBInr数据库。结果 获得了Hela细胞总蛋白质双向电泳图谱及蛋白质点的数字化信息,通过MALDI O-TOF-MS检测得到的肽质量指纹谱再经过网上公共数据的检索从而获得3个蛋白质点分别是α-葡萄糖苷酶(α-glucosidase)、γ-肌动蛋白(γ-actin)和过氧化物酶2(peroxiredoxin 2)。结论 Hela细胞总蛋白质双向电泳的分离效果较好,肽质量指纹谱法能有效地对Hela细胞的蛋白质斑点进行鉴定。

关键词: Hela细胞, 蛋白质组, 2-DE, MALDI O-TOF-MS, 肽质量指纹图谱

Abstract:

Objective To study the techniques of the isolation and identification of the proteins in Hela cells. Methods The proteins from Hela cells were extracted and isolated by two-dimensional electrophoresis(2-DE). The digital information of the protein spots was analyzed by a scanner and analysis software. Three spots of proteins in gel with different abundance were digested by an in-gel enzyme and the masses of the generated peptides were measured by matrix assisted laser desorption ionization orthogonal time of flight mass spectrometry(MALDI O-TOF-MS). The data obtained from peptide mass fingerprinting(PMF) were subjected to the protein database search. Results The 2-DE map of the proteins from Hela cells was generated by 2-DE, and the digital information of PMFs for the three protein spots were obtained by MALDI O-TOF-MS. Subsequently, these three protein spots were identified as α-glucosidase, γ-actin and peroxiredoxin 2 respectively through the database searching. Conclusion Peptide mass fingerprinting(PMF) is an applicable technique for the identification of proteins of Hela cells in combination with 2-D gel electrophoresis.

Key words: Hela cells, proteome, two-dimensional electrophoresis, MALDI O-TOF-MS, peptide mass fingerprinting

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