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[人鼻息肉二维凝胶电泳图谱的建立及蛋白质组学分析]

[Establishment of 2-dimensional gel electrophoresis map and analysis of proteomics from human nasal polyps].

作者信息

He Guang-xiang, Sun Hong, Wang Tian-sheng, Li Gui, Liu Huo-wang, Chen Yu

机构信息

Department of Otorhinolaryngology, Third Xiangya Hospital, Central South University, Changsha 410013, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2006 Aug;31(4):487-92.

Abstract

OBJECTIVE

To establish 2-dimensional polyacrylamide gel electrophoresis (2-DE) map from human nasal polyps and normal nasal mucosa, and to identify differential expression proteins of 2-DE map.

METHODS

Samples of nasal polyps and nasal mucosa (each sample group containing 7 cases) were obtained. The total proteins were extracted and separated by immobilized pH gradient (IPG)-based 2-DE. The silver-stained 2-DE was scanned with digital Imagescanner and analyzed with ImageMaster 2-DE Elite 4.01 software. To obtain peptide mass fingerprint (PMF) of differential protein spots, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) was used. The PMF was searched in Swiss-Prot and TreMBL database by Pept-Ident software, to identify differential expression proteins.

RESULTS

The well-resolved, reproducible 2-DE maps of nasal polyps and nasal mucosa were established. For the polyps tissues, the average proteins spot of three 2-DE maps was 825+/-78; and 682+/-96 spot was matched with the average matching rate of 82.7%. The average deviations of matched spot position were (1.13+/-0.16) mm in IEF direction and (1.45+/-0.21) mm in SDS-PAGE direction, respectively. For the nasal mucosa tissues, the average proteins spot of three 2-DE maps was 936+/-62; and 821+/-78 spots were matched with the average matching rate of 87.7%. After comparing the 2-DE maps of nasal polyps and nasal mucosa tissues, the protein spots were 1,458 and 1,617 respectively; and 1,026 protein spots were matched. Forty differential expression protein spots were incised from silver staining gel randomly and digested in the gel by TPCK-Trypsin. Thirty-four PMFs were obtained by MALDI-TOF-MS and 24 differential proteins were identified.

CONCLUSION

The well-resolved, reproducible 2-DE maps of human nasal polyps and nasal mucosa have been successfully established. Certain differential proteins related to the pathogenesis of human nasal polyps are identified.

摘要

目的

建立人鼻息肉和正常鼻黏膜的二维聚丙烯酰胺凝胶电泳(2-DE)图谱,并鉴定2-DE图谱中差异表达的蛋白质。

方法

获取鼻息肉和鼻黏膜样本(每组样本含7例)。提取总蛋白,采用基于固定化pH梯度(IPG)的2-DE进行分离。对银染的2-DE用数字图像扫描仪进行扫描,并用ImageMaster 2-DE Elite 4.01软件进行分析。为获得差异蛋白点的肽质量指纹(PMF),采用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)。用Pept-Ident软件在Swiss-Prot和TreMBL数据库中搜索PMF,以鉴定差异表达的蛋白质。

结果

成功建立了分辨良好、可重复的鼻息肉和鼻黏膜2-DE图谱。对于息肉组织,三张2-DE图谱的平均蛋白点数为825±78;匹配的点数为682±96,平均匹配率为82.7%。匹配点位置在IEF方向的平均偏差为(1.13±0.16)mm,在SDS-PAGE方向的平均偏差为(1.45±0.21)mm。对于鼻黏膜组织,三张2-DE图谱的平均蛋白点数为936±62;匹配的点数为821±78,平均匹配率为87.7%。比较鼻息肉和鼻黏膜组织的2-DE图谱后,蛋白点数分别为1458和1617;匹配的蛋白点数为1026。从银染凝胶中随机切下40个差异表达蛋白点,用TPCK-胰蛋白酶在凝胶内进行消化。通过MALDI-TOF-MS获得34个PMF,鉴定出24种差异蛋白。

结论

成功建立了分辨良好、可重复 的人鼻息肉和鼻黏膜2-DE图谱。鉴定出了某些与人鼻息肉发病机制相关的差异蛋白。

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