大酶B 破坏细菌的中心代谢和蛋白质合成,促进免疫细胞死亡程序
Farokh Dotiwala1, Sumit Sen Santara2, Andres Ariel Binker-Cosen3
1Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Vaccine Center, Wistar Institute, Philadelphia, PA 19104, USA.
Cell
|November 7, 2017
概括
人类细胞毒性淋巴细胞通过向必需蛋白质来杀死细菌. 这种多方面的攻击破坏了生命通路, 使细菌抵抗不太可能.
科学领域:
- 免疫学
- 微生物学
- 蛋白质组学
背景情况:
- 人类细胞毒性淋巴细胞使用含有花粉酶的细胞毒性颗粒消除细胞内微生物.
- 大酶蛋白酶通过破坏电子运输和失活防御来诱导细菌死亡,但也会导致无氧细菌的非氧化死亡.
研究的目的:
- 使用差异蛋白质学在三个不同的细菌物种中识别B基质.
- 了解细菌中granzyme B的保存目标以及对宿主防御的影响.
主要方法:
- 用差异蛋白质学分析了B基质.
- 这项研究集中在三个不相关的细菌上:大肠杆菌,单细胞菌和结核菌.
主要成果:
- 在不同物种的细菌生存中,Granzyme B可以分裂一组保护的蛋白质.
- 发现的关键基质包括参与重要生物合成和代谢途径的蛋白质.
- 针对蛋白质合成,折叠和降解至关重要的蛋白质,如氨基酸tRNA合成酶,核糖体蛋白质,辅助蛋白和Clp系统.
结论:
- Granzyme B采用多方策略,针对细菌中保存的重要途径.
- 细菌对重要功能的广泛向表明,细菌可能很难对细胞毒性淋巴细胞的攻击产生抵抗力.
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