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在宿主细胞内对刚地弓形虫蛋白质进行正交标记和纯化的新方法。

New method for the orthogonal labeling and purification of Toxoplasma gondii proteins while inside the host cell.

作者信息

Wier Gregory M, McGreevy Erica M, Brown Mark J, Boyle Jon P

机构信息

Department of Biological Sciences, Dietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Department of Biological Sciences, Dietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA

出版信息

mBio. 2015 Mar 10;6(2):e01628. doi: 10.1128/mBio.01628-14.

Abstract

UNLABELLED

Toxoplasma gondii is an obligate intracellular protozoan parasite that is capable of causing severe disease in immunocompromised humans. How T. gondii is able to modulate the host cell to support itself is still poorly understood. Knowledge pertaining to the host-parasite interaction could be bolstered by developing a system to specifically label parasite proteins while the parasite grows inside the host cell. For this purpose, we have created a strain of T. gondii that expresses a mutant Escherichia coli methionyl-tRNA synthetase (MetRS(NLL)) that allows methionine tRNA to be loaded with the azide-containing methionine analog azidonorleucine (Anl). Anl-containing proteins are susceptible to a copper-catalyzed "click" reaction to attach affinity tags for purification or fluorescent tags for visualization. The MetRS(NLL)-Anl system labels nascent T. gondii proteins in an orthogonal fashion, labeling proteins only in MetRS(NLL)-expressing parasites. This system should be useful for nonradioactive pulse-chase studies and purification of nascently translated proteins. Although this approach allows labeling of a diverse array of parasite proteins, secreted parasite proteins appear to be only minimally labeled in MetRS(NLL)-expressing T. gondii. The minimal labeling of secreted proteins is likely a consequence of the selective charging of the initiator tRNA (and not the elongator methionine tRNA) by the heterologously expressed bacterial MetRS.

IMPORTANCE

Studying how T. gondii modifies the host cell to permit its survival is complicated by the complex protein environment of the host cell. The approach presented in this article provides the first method for specific labeling of T. gondii proteins while the parasite grows inside the host cell. We show that this approach is useful for pulse-chase labeling of parasite proteins during in vitro growth. It should also be applicable during in vivo infections and in other apicomplexan parasites, including Plasmodium spp.

摘要

未标记

刚地弓形虫是一种专性细胞内原生动物寄生虫,能够在免疫功能低下的人类中引发严重疾病。目前对于刚地弓形虫如何调节宿主细胞以支持自身生长的了解仍然有限。通过开发一种在寄生虫于宿主细胞内生长时特异性标记寄生虫蛋白质的系统,可以加强对宿主-寄生虫相互作用的认识。为此,我们构建了一种刚地弓形虫菌株,该菌株表达一种突变的大肠杆菌甲硫氨酰-tRNA合成酶(MetRS(NLL)),它能使甲硫氨酸tRNA装载含叠氮基的甲硫氨酸类似物叠氮亮氨酸(Anl)。含Anl的蛋白质易受铜催化的“点击”反应影响,从而连接用于纯化的亲和标签或用于可视化的荧光标签。MetRS(NLL)-Anl系统以正交方式标记新生的刚地弓形虫蛋白质,仅在表达MetRS(NLL)的寄生虫中标记蛋白质。该系统对于非放射性脉冲追踪研究和新生翻译蛋白质的纯化应该是有用的。尽管这种方法能够标记多种寄生虫蛋白质,但在表达MetRS(NLL)的刚地弓形虫中,分泌的寄生虫蛋白质似乎仅被极少量标记。分泌蛋白的少量标记可能是由于异源表达的细菌MetRS对起始tRNA(而非延伸甲硫氨酸tRNA)的选择性加载所致。

重要性

研究刚地弓形虫如何改变宿主细胞以使其存活因宿主细胞复杂的蛋白质环境而变得复杂。本文介绍的方法提供了第一种在寄生虫于宿主细胞内生长时特异性标记刚地弓形虫蛋白质的方法。我们表明这种方法对于体外生长期间寄生虫蛋白质的脉冲追踪标记是有用的。它也应该适用于体内感染以及其他顶复门寄生虫,包括疟原虫属。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2937/4453564/d518dd03548d/mbo0021522210001.jpg

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