Liu Hong-Li, Xia Qing-You, Hou Yong, Zhao Ping, Zou Yong, Guan Jian
The Key Sericultural Laboratory of Agricultural Ministry, Southwest University, Chongqing 400716, China.
Sheng Wu Gong Cheng Xue Bao. 2007 Jan;23(1):112-6.
We separated proteins of the middle silk gland through high resolution two-dimensional polyacrylamide gel electrophesis, and identified the high expressional proteins using MALDI-TOF-MS and analyzed the PMF in protein database by GPMAW( General Protein/Mass Analysis for Windows) . The protein database was forecasted through silkworm genome database. More than 500 spots were obtained from each gel by silver stain and more than 100 protein spots were obtained from gel by Coomassie brilliant blue stain. Most of them were distributed in the area from 15kD to 90kD with pH 3.5-7. Among the 25 Coomassie brilliant blue stained spots identified by MALDI-TOF-MS, more than 60% have relatively strong signal. Comparing with the result of using Mascot, the method using PMF database of silkworm not only can identify some known proteins, but also can identify some unknown proteins that have been forecasted in silkworm genome database. Accordingly, we founded a complete set of method that fit for researching proteome of silkworm.
我们通过高分辨率二维聚丙烯酰胺凝胶电泳分离中部丝腺蛋白,利用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)鉴定高表达蛋白,并通过GPMAW(适用于Windows的通用蛋白质/质量分析软件)在蛋白质数据库中分析肽质量指纹图谱(PMF)。蛋白质数据库通过家蚕基因组数据库预测。银染法从每张凝胶上获得500多个斑点,考马斯亮蓝染色法从凝胶上获得100多个蛋白质斑点。它们大多分布在pH值为3.5至7、分子量为15kD至90kD的区域。在通过MALDI-TOF-MS鉴定的25个考马斯亮蓝染色斑点中,超过60%具有相对较强的信号。与使用Mascot的结果相比,利用家蚕PMF数据库的方法不仅可以鉴定一些已知蛋白质,还可以鉴定在家蚕基因组数据库中预测的一些未知蛋白质。据此,我们建立了一套适合研究家蚕蛋白质组的完整方法。