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作 者:Tian-Yi Ying Jun-Jun Wang Heng-Liang Wang Er-Ling Feng Kai-Hua Wei Liu-Yu Huang Pei-Tang Huang Cui-Fen Huang
机构地区:[1]Beijing Institute of Biotechnology, State Key Lab of Pathogen and Biosecurity, Beijing 100071, China [2]Beijing Institute of Pharmaceutical Chemistry, Beijing 102205, China
出 处:《World Journal of Gastroenterology》2005年第43期6880-6883,共4页世界胃肠病学杂志(英文版)
基 金:Supported by the Capital "248" Key Innovation Project, No. H010210360119, State Basic Research Development Program of China No. 973 Program, G1999054103 and 2005CB22904 and National Natural Science Foundation of China No. 30470101
摘 要:AIM: To screen the immunogenic membrane proteins of Shigella Aexneri 2a 2457T. METHODS: The routine two-dimensional polyacrylamide gel electrophoresis (2-DE) and Western blotting were combined to screen immunogenic proteins of S. Aexneri 2a 2457T. Serum was gained from rabbits immunized with the same bacteria. Immunogenic spots were cut out from the polyacrylamide gel and digested by trypsin in-gel. Matrix-assisted laser desorption/ionization time of flight-mass spectrometry (MALDI-TOF-MS) was performed to determine the molecular weight of peptides. Electrospray ionization (ESI-MS/MS) was performed to determine the sequences of the interesting peptides. RESULTS: A total of 20 spots were successfully identified from Coomassie brilliant blue stained gels representing 13 protein entries, 5 known antigens and 8 novel antigens. A hypothetical protein (YaeT) was detected, which might be a candidate target of vaccine. CONCLUSION: Membrane proteins of S. flexneri 2a 2457T were successfully observed by 2-DE. Several known and novel antigens were identified by mass spectrum.AIM: To screen the immunogenic membrane proteins ofShigella flexneri 2a 2457T.METHODS: The routine two-dimensional polyacrylamidegel electrophoresis (2-DE) and Western blotting werecombined to screen immunogenic proteins of S. flexneri2a 2457T. Serum was gained from rabbits immunizedwith the same bacteria. Immunogenic spots werecut out from the polyacrylamide gel and digested bytrypsin in-gel. Matrix-assisted laser desorption/ionizationtime of flight-mass spectrometry (MALDI-TOF-MS)was performed to determine the molecular weight ofpeptides. Electrospray ionization (ESI-MS/MS) wasperformed to determine the sequences of the interestingpeptides.RESULTS: A total of 20 spots were successfullyidentified from Coomassie brilliant blue stained gelsrepresenting 13 protein entries, 5 known antigens and8 novel antigens. A hypothetical protein (YaeT) wasdetected, which might be a candidate target of vaccine.CONCLUSION: Membrane proteins of S. flexneri 2a2457T were successfully observed by 2-DE. Severalknown and novel antigens were identified by massspectrum.
关 键 词:Shigella flexneri 2a 2457T IMMUNOPROTEOMICS Membrane proteins
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