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通过质谱法鉴定弓形虫ROP1的前体成熟加工位点。

Identification of the pro-mature processing site of Toxoplasma ROP1 by mass spectrometry.

作者信息

Bradley P J, Boothroyd J C

机构信息

Department of Microbiology and Immunology, Stanford University School of Medicine, CA 94305-5124, USA.

出版信息

Mol Biochem Parasitol. 1999 May 15;100(1):103-9. doi: 10.1016/s0166-6851(99)00035-3.

Abstract

The rhoptries are specialized secretory organelles that function during host cell invasion in the obligate intracellular parasite Toxoplasma gondii. All T. gondii rhoptry proteins studied to date are synthesized as pro-proteins that are then processed to their mature forms. To understand the role of the pro region in rhoptry protein function, we have precisely defined the processing site of the pro-region of the rhoptry protein ROP1. Efforts to determine such processing sites have been prevented by blocked N-termini of mature proteins isolated from T. gondii. To overcome this problem, we have used an engineered form of ROP1 and mass spectrometry to demonstrate that proROP1 is processed to its mature form between the glutamic acid at position 83 and alanine at position 84. These data also show that mature ROP1 lacks substantial post-translational modifications, a result which has important implications for targeting of rhoptry proteins.

摘要

棒状体是专化的分泌细胞器,在专性细胞内寄生虫刚地弓形虫入侵宿主细胞的过程中发挥作用。迄今为止研究的所有刚地弓形虫棒状体蛋白都是以前体蛋白的形式合成的,然后加工成成熟形式。为了了解前体区域在棒状体蛋白功能中的作用,我们精确地确定了棒状体蛋白ROP1前体区域的加工位点。从刚地弓形虫中分离出的成熟蛋白的N端封闭,阻碍了确定此类加工位点的工作。为克服这一问题,我们使用了ROP1的工程形式和质谱法,证明前体ROP1在第83位的谷氨酸和第84位的丙氨酸之间被加工成其成熟形式。这些数据还表明,成熟的ROP1缺乏大量的翻译后修饰,这一结果对棒状体蛋白的靶向具有重要意义。

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