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Leucine-rich-repeat-containing variable lymphocyte receptors as modules to target plant-expressed proteins

机译:富含亮氨酸重复序列的可变淋巴细胞受体作为靶向植物表达蛋白的模块

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BackgroundThe ability to target and manipulate protein-based cellular processes would accelerate plant research; yet, the technology to specifically and selectively target plant-expressed proteins is still in its infancy. Leucine-rich repeats (LRRs) are ubiquitously present protein domains involved in mediating protein–protein interactions. LRRs confer the binding specificity to the highly diverse variable lymphocyte receptor (VLR) antibodies (including VLRA, VLRB and VLRC types) that jawless vertebrates make as the functional equivalents of jawed vertebrate immunoglobulin-based antibodies. ResultsIn this study, VLRBs targeting an effector protein from a plant pathogen, HopM1, were developed by immunizing lampreys and using yeast surface display to select for high-affinity VLRBs. HopM1-specific VLRBs (VLRM1) were expressed in planta in the cytosol, the trans -Golgi network, and the apoplast. Expression of VLRM1 was higher when the protein localized to an oxidizing environment that would favor disulfide bridge formation (when VLRM1 was not localized to the cytoplasm), as disulfide bonds are necessary for proper VLR folding. VLRM1 specifically interacted in planta with HopM1 but not with an unrelated bacterial effector protein while HopM1 failed to interact with a non-specific VLRB. ConclusionsIn the future, VLRs may be used as flexible modules to bind proteins or carbohydrates of interest in planta , with broad possibilities for their use by binding directly to their targets and inhibiting their action, or by creating chimeric proteins with new specificities in which endogenous LRR domains are replaced by those present in VLRs.
机译:背景靶向和操纵基于蛋白质的细胞过程的能力将加速植物研究。但是,特异性和选择性靶向植物表达的蛋白质的技术仍处于起步阶段。富含亮氨酸的重复序列(LRR)是普遍存在的介导蛋白质与蛋白质相互作用的蛋白质结构域。 LRR赋予与无颚脊椎动物作为具有颚脊椎动物免疫球蛋白的抗体的功能等同物的高度多样化的可变淋巴细胞受体(VLR)抗体(包括VLRA,VLRB和VLRC类型)的结合特异性。结果在这项研究中,通过免疫七lamp鳗并使用酵母表面展示来选择高亲和性VLRB,从而开发了针对来自植物病原体HopM1的效应蛋白的VLRB。 HopM1特异性VLRB(VLR M1 )在植物中的细胞质,反-高尔基体网络和质外体中表达。当蛋白质定位于有利于二硫键形成的氧化环境时(当VLR M1 不定位于细胞质时),VLR M1 的表达较高,因为二硫键是正确折叠VLR所必需。 VLR M1 在植物中与HopM1特异性相互作用,但不与无关的细菌效应蛋白相互作用,而HopM1未能与非特异性VLRB相互作用。结论未来,VLRs可以用作结合植物中目的蛋白或碳水化合物的灵活模块,通过直接结合其靶标并抑制其作用,或通过产生具有新特异性的内源LRR嵌合蛋白来广泛使用它们。域被VLR中存在的域替换。

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