广西科学
廣西科學
엄서과학
GUANGXI SCIENCES
2014年
2期
103-107
,共5页
岑卫健%甘永亮%于凯%付强%韦宇拓%姜伯乐
岑衛健%甘永亮%于凱%付彊%韋宇拓%薑伯樂
잠위건%감영량%우개%부강%위우탁%강백악
Xcc%蛋白质表达谱%LC-MS/MS%LTQ-Orbitrap
Xcc%蛋白質錶達譜%LC-MS/MS%LTQ-Orbitrap
Xcc%단백질표체보%LC-MS/MS%LTQ-Orbitrap
Xcc%proteome profile%LC-MS/MS%LTQ-Orbitrap
【目的】建立十字花科黑腐病菌(Xanthomonas campestris pv.campestris ,Xcc )的蛋白质组学研究平台,用于分离、鉴定该菌的致病相关蛋白质。【方法】Xcc 8004经过液体培养,分别提取胞内蛋白质和胞外蛋白质,对所有蛋白质进行液体酶解,通过强阳离子交换色谱预分离多肽混合物,预分离后的馏分采用 EASY-nLC 结合LTQ-Orbitrap 质谱鉴定蛋白质表达谱。【结果】建立了基于 bottom-up 策略的蛋白质组鉴定方法,采用第一维离子交换预分离和第二维反相色谱分离结合,实现了高通量鉴定蛋白质组表达谱的技术体系。通过 SEQUEST 检索,在胞内蛋白质样品中共鉴定蛋白质数目为1595个,胞外蛋白质样品共鉴定蛋白质数目为1241个。【结论】建立的 LC-MS/MS 方法适合用于十字花科黑腐病菌蛋白质组学的研究,为研究微生物植物相互作用奠定了方法与理论基础。
【目的】建立十字花科黑腐病菌(Xanthomonas campestris pv.campestris ,Xcc )的蛋白質組學研究平檯,用于分離、鑒定該菌的緻病相關蛋白質。【方法】Xcc 8004經過液體培養,分彆提取胞內蛋白質和胞外蛋白質,對所有蛋白質進行液體酶解,通過彊暘離子交換色譜預分離多肽混閤物,預分離後的餾分採用 EASY-nLC 結閤LTQ-Orbitrap 質譜鑒定蛋白質錶達譜。【結果】建立瞭基于 bottom-up 策略的蛋白質組鑒定方法,採用第一維離子交換預分離和第二維反相色譜分離結閤,實現瞭高通量鑒定蛋白質組錶達譜的技術體繫。通過 SEQUEST 檢索,在胞內蛋白質樣品中共鑒定蛋白質數目為1595箇,胞外蛋白質樣品共鑒定蛋白質數目為1241箇。【結論】建立的 LC-MS/MS 方法適閤用于十字花科黑腐病菌蛋白質組學的研究,為研究微生物植物相互作用奠定瞭方法與理論基礎。
【목적】건립십자화과흑부병균(Xanthomonas campestris pv.campestris ,Xcc )적단백질조학연구평태,용우분리、감정해균적치병상관단백질。【방법】Xcc 8004경과액체배양,분별제취포내단백질화포외단백질,대소유단백질진행액체매해,통과강양리자교환색보예분리다태혼합물,예분리후적류분채용 EASY-nLC 결합LTQ-Orbitrap 질보감정단백질표체보。【결과】건립료기우 bottom-up 책략적단백질조감정방법,채용제일유리자교환예분리화제이유반상색보분리결합,실현료고통량감정단백질조표체보적기술체계。통과 SEQUEST 검색,재포내단백질양품중공감정단백질수목위1595개,포외단백질양품공감정단백질수목위1241개。【결론】건립적 LC-MS/MS 방법괄합용우십자화과흑부병균단백질조학적연구,위연구미생물식물상호작용전정료방법여이론기출。
[Objective ]A proteomics technical platform of Xanthomonas campestris pv . campestris (Xcc )was established for the separation and identification of pathogenic bacteria associated proteins.[Methods]The intracellular proteins and extracellular proteins of Xcc 8004 strains were extracted after liquid cultured.After in-solution digestion of total proteins,the peptides mixtures were separated by strong cation exchange (SCX)column.The proteome pro-files were acquired by EASY-nLC combined LTQ-Orbitrap mass spectrometer.[Results]Based on bottom-up method,the proteins were analyzed by cation exchange column and nanoflow re-versed-phase liquid chromatography.The high proteomic profile identification was realized.The mass spectrometry data were searched with SEQUEST.As a result,a total of 1595 proteins were obtained from intracellular proteins and a total of 1241 proteins were obtained from extra-cellular proteins.[Conclusion]LC-MS/MS work-flow could be utilized successfully in the pro-teomics research of Xcc pathogenesis,which pro-vides the basis for studing the interaction of mi-crobe and plant.