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鼠疫耶尔森氏菌及其靶向外膜蛋白 H 酪氨酸磷酸酶(YopH)的方法。

Yersinia pestis and approaches to targeting its outer protein H protein-tyrosine phosphatase (YopH).

机构信息

Chemical Biology Laboratory, Frederick National Laboratory for Cancer Research, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, U.S.A.

出版信息

Curr Med Chem. 2012;19(33):5726-34. doi: 10.2174/092986712803988866.

DOI:10.2174/092986712803988866
PMID:22934808
Abstract

Plague is an infectious disease with a high mortality rate that has repeatedly impacted human society. It remains a threat in many parts of the world today. Plague is caused by the bacterium, Yersinia pestis (Y. pestis), which has as one of its required virulence factors, the protein-tyrosine phosphatase, YopH. Therefore, YopH represents a potential target for the treatment of Y. pestis infection. Recent recognition of Y. pestis as a possible bioterrorism agent and the fact that it is still the cause of endemic disease around the world make it an important object of study and heighten the need for new anti-plague agents. The current review covers aspects of plague and its historical occurrence and summarizes approaches to developing YopH inhibitors.

摘要

鼠疫是一种死亡率很高的传染病,曾多次对人类社会造成影响。时至今日,它在世界上的许多地方仍然构成威胁。鼠疫是由细菌鼠疫耶尔森菌(Yersinia pestis,Y. pestis)引起的,该细菌的一种必需毒力因子是蛋白酪氨酸磷酸酶 YopH。因此,YopH 代表了治疗鼠疫耶尔森菌感染的潜在靶点。最近,人们认识到鼠疫耶尔森菌可能是一种生物恐怖主义制剂,而且它仍然是世界各地地方性疾病的病因,这使得它成为一个重要的研究对象,并增加了对新型抗鼠疫制剂的需求。本综述涵盖了鼠疫及其历史发生的各个方面,并总结了开发 YopH 抑制剂的方法。

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Yersinia pestis and approaches to targeting its outer protein H protein-tyrosine phosphatase (YopH).鼠疫耶尔森氏菌及其靶向外膜蛋白 H 酪氨酸磷酸酶(YopH)的方法。
Curr Med Chem. 2012;19(33):5726-34. doi: 10.2174/092986712803988866.
2
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Yersinia pestis CO92 delta yopH is a potent live, attenuated plague vaccine.鼠疫耶尔森菌CO92缺失yopH基因株是一种有效的减毒活鼠疫疫苗。
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Biomolecular Interactions of small-molecule inhibitors affecting the YopH protein tyrosine phosphatase.小分子抑制剂对 YopH 蛋白酪氨酸磷酸酶的生物分子相互作用。
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引用本文的文献

1
High-resolution crystal structures of the D1 and D2 domains of protein tyrosine phosphatase epsilon for structure-based drug design.蛋白酪氨酸磷酸酶 epsilon 的 D1 和 D2 结构域的高分辨率晶体结构,用于基于结构的药物设计。
Acta Crystallogr D Struct Biol. 2018 Oct 1;74(Pt 10):1015-1026. doi: 10.1107/S2059798318011919. Epub 2018 Oct 2.
2
Aurintricarboxylic acid structure modifications lead to reduction of inhibitory properties against virulence factor YopH and higher cytotoxicity.金精三羧酸结构修饰导致对毒力因子YopH的抑制特性降低以及更高的细胞毒性。
World J Microbiol Biotechnol. 2016 Oct;32(10):163. doi: 10.1007/s11274-016-2123-3. Epub 2016 Aug 25.
3
Chicoric acid binds to two sites and decreases the activity of the YopH bacterial virulence factor.
菊苣酸与两个位点结合并降低YopH细菌毒力因子的活性。
Oncotarget. 2016 Jan 19;7(3):2229-38. doi: 10.18632/oncotarget.6812.
4
Redox process is crucial for inhibitory properties of aurintricarboxylic acid against activity of YopH: virulence factor of Yersinia pestis.氧化还原过程对于金精三羧酸抑制鼠疫耶尔森氏菌的毒力因子YopH活性的特性至关重要。
Oncotarget. 2015 Jul 30;6(21):18364-73. doi: 10.18632/oncotarget.4625.
5
Yersinia pestis: mechanisms of entry into and resistance to the host cell.鼠疫耶尔森菌:进入宿主细胞和抵抗宿主细胞的机制。
Front Cell Infect Microbiol. 2013 Dec 24;3:106. doi: 10.3389/fcimb.2013.00106. eCollection 2013.