抗日本血吸虫生殖抗原SIEA 26-28ku组分的质谱分析  

MALDI-TOF-MS analysis of the SIEA 26-28 ku components against Schisitosoma japonicum fecundity immunity

作　　者：汪世平[1] 刘立鹏[1] 钟飞[2] 徐绍锐[1] 彭先楚[1] 李文凯[1] 何卓[1] 

机构地区：[1]中南大学湘雅医学院血吸虫病研究室,湖南长沙410078 [2]吉首大学,湖南吉首416000

出　　处：《中国病原生物学杂志》2008年第10期745-748,769,共5页Journal of Pathogen Biology

基　　金：国家重点基础研究发展计划(973)资助项目(No.2007CB513108);湖南省“十一·五”重大专项(No.2006SK1001);湖南省“十一·五”重点学科建设专项经费(No.07-985-2)联合资助项目

摘　　要：目的筛选确定抗日本血吸虫生殖功能抗原SIEA26-28 ku的编码基因。方法采用固相pH梯度双向凝胶电泳分离日本血吸虫未成熟卵可溶性抗原(SIEA),选择SIEA 26-28 ku免疫血清识别信号较强的SIEA-2D蛋白质斑点(65～73号)采样,消化处理后进行质谱与生物学信息分析。结果从SIEA-2D图谱上共获得1037个蛋白质斑点;通过MALDI-TOF-MS对其进行肽指纹图谱分析后获得了7张肽指纹图谱。通过PeptIdent软件检索SWISS-PROT数据库,发现有意义的血吸虫同源蛋白质11个,这些同源蛋白质部分与细胞代谢或蛋白质合成代谢相关,部分与核苷酸代谢有关,其中编号为SIEA-2D66为日本血吸虫次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HGPRT),SIEA-2D71为琥珀酸脱氢酶铁硫蛋白(SDISP),SIEA-2D73为谷胱甘肽-S-转移酶(GST),其同源程度分别为37.2%、18.7%和22.9%。结论初步获得与抗日本血吸虫生殖功能抗原SIEAn 26～28 ku相关的编码基因HGPRT、SDISP和GST。Objective To identify and get the encoding gene of the SIEA 26-28 ku molecule against Schisitosoma japoni cure fecundity immunity. Methods The proteome group of SIEA was separated and identified by a series of methods, including immobilized pH gradient two dimensional polyacrylamide gel electrophoresis （2-D） , silver staining etc. Spots of SIEA-2D65-73, which showed a strong immunoreactivity with the mono specific anti-sera against SIEA26 28 ku components, were selected and incised from silver staining gel after digested in-gel by trypsin, and used to analyzed by the ma- trix assisted laser desorption/ionization time of flying mass spectrometry （MALDI-TOF MS） and bioinformatics analysis. Results The silver stained 2-DE profile of SIEA demonstrated 1 037 protein spots. Seven peptide mass fingerprint （PMF） maps were displayed by MALDI TOF-MS. The typical peptide masses were searched from the SWISS-PROT database with PeptIdent software. Eleven proteins with significant homogeneity were preliminarily identified, which included cell metabolism-related proteins, enzymes related to the proteins syntheses, and another of them were responsible for the salvage pathway of purine bases needed for nucleotide metabolism. Three of these were preliminarily identified proteins including the SIEA-2D66 （hypoxanthine-guanine phosphoribosyl transferase, HGPRT）, SIEA 2D71 （succinate dehydrogenase iron sulfur protein, SDISP） and SIEA-2D73 （glutathione-S-transferase, GST） shared a homogeneity of 37.2 %, 18.7% and 22.9 %, respectively. Conclusion HGPRT, SDISP and GST are relative to the encoding gene of SIEA 26-28 ku molecule against S. japonicum fecundity immunity.

关 键 词：血吸虫 日本 未成熟卵可溶性抗原 SIEA 26-28 ku分子 肽指纹图谱分析 

分 类 号：R383.24[医药卫生—医学寄生虫学]