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New Method for the Orthogonal Labeling and Purification of Toxoplasma gondii Proteins While Inside the Host Cell

机译:宿主细胞内弓形虫蛋白质的正交标记和纯化的新方法

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ABSTRACT 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.
机译:摘要弓形虫是专性的细胞内原生动物寄生虫,能够在免疫功能低下的人类中引起严重的疾病。 T.gondii如何能够调节宿主细胞以支持其自身仍知之甚少。有关寄生虫在宿主细胞内生长的同时,通过开发一种系统专门标记寄生虫蛋白的系统,可以增强有关宿主-寄生虫相互作用的知识。为此目的,我们创建了一种能表达突变大肠杆菌的甲硫氨酸甲硫氨酸-tRNA合成酶(MetRS〜(NLL))的拟南芥T.Δgdii菌株,该菌株可使甲硫氨酸tRNA上载有含叠氮化物的甲硫氨酸类似物azidonorleucine(Anl) 。含Anl的蛋白质容易受到铜催化的“喀哒”反应的影响,以附着亲和标签进行纯化或荧光标签进行可视化。 MetRS〜(NLL)-Anl系统以正交方式标记刚生的T.?gondii蛋白,仅在表达MetRS〜(NLL)的寄生虫中标记蛋白。该系统对于非放射性脉冲追踪研究和新生翻译蛋白的纯化应该是有用的。尽管这种方法可以标记各种各样的寄生虫蛋白,但是分泌的寄生虫蛋白似乎在表达MetRS〜(NLL)的T.gondii中只有极少的标记。分泌蛋白的最低限度标记可能是由于异源表达的细菌MetRS对引发剂tRNA(而不是延伸子蛋氨酸tRNA)进行选择性充电所致。重要由于宿主细胞的蛋白质环境复杂,研究贡氏梭菌如何修饰宿主细胞以使其存活。本文介绍的方法提供了第一种方法,可以在寄生虫在宿主细胞内部生长的同时对T.gondii蛋白进行特异性标记。我们表明,这种方法可用于体外生长过程中的寄生虫蛋白的脉冲追踪标记。它也应该适用于体内感染和其他疟原虫寄生虫,包括疟原虫属。

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