南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2010年
2期
341-344
,共4页
谢妮%蔡茵莎%吴瑾滨%刘建军
謝妮%蔡茵莎%吳瑾濱%劉建軍
사니%채인사%오근빈%류건군
人类巨细胞病毒%病毒感染%蛋白质组学%差异表达
人類巨細胞病毒%病毒感染%蛋白質組學%差異錶達
인류거세포병독%병독감염%단백질조학%차이표체
human cytomegalovirus,infection%proteomics%differential expression
目的 建立人类巨细胞病毒(HCMV)感染小鼠脑组织前后的比较蛋白质组学双向电泳技术研究体系.方法 昆明系小鼠40只,随机分为两组:实验对照组(20只)和病毒感染组(20只),在接种HCMVAD_(169)株30d后,取小鼠脑组织,研磨、超声裂解、抽提蛋白,采用双向凝胶电泳分离,进行染色,Image Master 2D Platinum软件分析、识别差异表达蛋白质,应用基质辅助激光解吸电离飞行时间质谱得到相应肽质量指纹图谱,搜索数据库鉴定部分差异蛋白质点,并对其中部分蛋白质的表达进行免疫印迹的验证.结果 从双向电泳图谱上获得蛋白质斑点:实验对照组(1096±82)个,感染HCMV组(1210±101)个,发现显著差异点36个,对其中6个点进行了筛选鉴定;免疫印迹实验结果也较为吻合.结论利用蛋白质组学技术,检测正常小鼠脑组织及HCMV感染的小鼠脑组织的差异蛋白质,为疾病的早期诊断、致病机制及有效药物靶点的发现提供实验和理论依据.
目的 建立人類巨細胞病毒(HCMV)感染小鼠腦組織前後的比較蛋白質組學雙嚮電泳技術研究體繫.方法 昆明繫小鼠40隻,隨機分為兩組:實驗對照組(20隻)和病毒感染組(20隻),在接種HCMVAD_(169)株30d後,取小鼠腦組織,研磨、超聲裂解、抽提蛋白,採用雙嚮凝膠電泳分離,進行染色,Image Master 2D Platinum軟件分析、識彆差異錶達蛋白質,應用基質輔助激光解吸電離飛行時間質譜得到相應肽質量指紋圖譜,搜索數據庫鑒定部分差異蛋白質點,併對其中部分蛋白質的錶達進行免疫印跡的驗證.結果 從雙嚮電泳圖譜上穫得蛋白質斑點:實驗對照組(1096±82)箇,感染HCMV組(1210±101)箇,髮現顯著差異點36箇,對其中6箇點進行瞭篩選鑒定;免疫印跡實驗結果也較為吻閤.結論利用蛋白質組學技術,檢測正常小鼠腦組織及HCMV感染的小鼠腦組織的差異蛋白質,為疾病的早期診斷、緻病機製及有效藥物靶點的髮現提供實驗和理論依據.
목적 건립인류거세포병독(HCMV)감염소서뇌조직전후적비교단백질조학쌍향전영기술연구체계.방법 곤명계소서40지,수궤분위량조:실험대조조(20지)화병독감염조(20지),재접충HCMVAD_(169)주30d후,취소서뇌조직,연마、초성렬해、추제단백,채용쌍향응효전영분리,진행염색,Image Master 2D Platinum연건분석、식별차이표체단백질,응용기질보조격광해흡전리비행시간질보득도상응태질량지문도보,수색수거고감정부분차이단백질점,병대기중부분단백질적표체진행면역인적적험증.결과 종쌍향전영도보상획득단백질반점:실험대조조(1096±82)개,감염HCMV조(1210±101)개,발현현저차이점36개,대기중6개점진행료사선감정;면역인적실험결과야교위문합.결론이용단백질조학기술,검측정상소서뇌조직급HCMV감염적소서뇌조직적차이단백질,위질병적조기진단、치병궤제급유효약물파점적발현제공실험화이론의거.
Objective To establish the two-dimensional electrophoresis profiles with high resolution and reproducibility from the brain tissues of mice with human cytomegalovirus (HCMV) infection, Methods Forty Kunming mice were randomized into HCMV infection group (n=20) with HCMVAD169 injection and control group (n=20) with saline injection in the brain.Thirty days after the injections, the brain tissue of the mice were taken and the protein fractions were isolated by two-dimensional gel electrophoresis (2-DE). Image Master 2D software was used to identify the differentially expressed proteins, and the peptide mass fingerprint (PMF) data were obtained for identification of the differential protein spots via database searching.Western blotting was performed to verify the expressions of some of the differential proteins. Results and Conclusion The 2-D maps of the brain tissues with high Well resolution and reproducibility were obtained. Some of the differentially expressed proteins identified by mass spectrometry (MS) matched their counterparts in the SWISS-2DPAGE database. Western blotting analyses verified the differential expression of the individual proteins. These data can be of value for studying the diagnosis, pathogenesis and effective therapeutic targets of the disease.