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通过在本氏烟草中瞬时表达来纯化效应蛋白-靶蛋白复合物

Purification of effector-target protein complexes via transient expression in Nicotiana benthamiana.

作者信息

Win Joe, Kamoun Sophien, Jones Alexandra M E

机构信息

The Sainsbury Laboratory, John Innes Centre, Norwich, UK.

出版信息

Methods Mol Biol. 2011;712:181-94. doi: 10.1007/978-1-61737-998-7_15.

Abstract

Effectors of plant pathogens play important roles in not only pathogenesis but also plant immunity. Plant pathogens use these effectors to manipulate host cells for colonization, and their activities likely influence the evolution of plant immune responses. Analyses of genome sequences revealed that oomycete pathogens, such as Phytophthora spp., possess hundreds of RXLR effectors that are thought to be delivered into the host cells and hence function inside the cells by interacting with the host protein complexes. This article describes a co-immunoprecipitation protocol aimed at identifying putative target complexes of the effectors by transiently overexpressing the tagged effectors in planta. The identification of the eluted protein complexes was achieved by LC-MS/MS mass spectrometry and peptide spectrum matching.

摘要

植物病原体的效应子不仅在致病过程中发挥重要作用,而且在植物免疫中也起着重要作用。植物病原体利用这些效应子操纵宿主细胞以实现定殖,并且它们的活动可能影响植物免疫反应的进化。基因组序列分析表明,卵菌病原体,如疫霉属物种,拥有数百种RXLR效应子,这些效应子被认为会被递送到宿主细胞中,并通过与宿主蛋白复合物相互作用在细胞内发挥功能。本文描述了一种免疫共沉淀方案,旨在通过在植物中瞬时过表达带标签的效应子来鉴定效应子的假定靶标复合物。通过液相色谱-串联质谱(LC-MS/MS)和肽谱匹配来实现对洗脱的蛋白复合物的鉴定。

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