期刊文献+

以蛋白激酶G为靶点的抗结核药物筛选模型

Anti-tuberculosis Drugs Screening Model Targeting to PknG
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摘要 结核分枝杆菌在被巨噬细胞吞噬、形成吞噬体后,可以通过阻止吞噬体的成熟及其与溶酶体的融合,而使其自身不被溶酶体酶降解,从而在巨噬细胞内长期存留下来。此时的细菌代谢活动降至最低,生长繁殖几乎停止,不易被抗菌药物杀灭,这种类似于休眠的长期存活状态被称为“持留”状态。
作者 邱并生
出处 《微生物学通报》 CAS CSCD 北大核心 2010年第2期311-311,共1页 Microbiology China
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参考文献4

  • 1Walburger A, Koul A, Ferrari G, et al. Protein kinase G from pathogenic mycobacteria promotes survival within macrophages. Science, 2004(304): 1800-1804. 被引量:1
  • 2Szekely R, Waczek F, Szabadkai I, et al. A novel drug discovery concept for tuberculosis: inhibition of bacterial and host cell signaling. Immunol Lett, 2008, 116(2): 225-231. 被引量:1
  • 3Hegymegi-Barakonyi B, Szekely R, Varga Z, et al. Signalling inhibitors against Mycobacterium tuberculosis - early days of a new therapeutic concept in tuberculosis. Curr Med Chem, 2008, 15(26): 2760-2770. 被引量:1
  • 4邵天舒,魏玉珍,李秋萍,赵莉莉,岑山,余利岩.以蛋白激酶G为靶点的抗结核药物筛选模型的建立和初步应用[J].微生物学通报,2010,37(2):312-318. 被引量:4

二级参考文献11

  • 1邹文进,刘祖国,蒋爱华,李朝阳.多西环素诱导单核细胞系THP-1凋亡的实验研究[J].中国病理生理杂志,2007,23(6):1195-1198. 被引量:6
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  • 7Walburger A, Koul A, Ferrari G, et al. Protein kinase G from pathogenic mycobacteria promotes survival within macrophages. Science, 2004(304): 1800-1804. 被引量:1
  • 8Szekely R, Waczek F, Szabadkai I, et al. A novel drug discovery concept for tuberculosis: inhibition of bacterial and host cell signaling. Immunol Lett, 2008, 116(2): 225-231. 被引量:1
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  • 10Scherr N, Muller P, Perisa D, et al. Survival of pathogenic mycobacteria in macrophages is mediated through autophosphorylation of protein kinase G. J Bacteriol, 2009, 191(14): 4546-4554. 被引量:1

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