Hijazi May, Roujol David, Nguyen-Kim Huan, Del Rocio Cisneros Castillo Liliana, Saland Estelle, Jamet Elisabeth, Albenne Cécile
Université de Toulouse; UPS; UMR 5546, Laboratoire de Recherche en Sciences Végétales; BP 42617 Auzeville, F-31326 Castanet-Tolosan, France CNRS; UMR 5546; BP 42617, F-31326 Castanet-Tolosan, France.
Division of Tumor Virology (F010), German Cancer Research Center DKFZ, Im Neuenheimer Feld 242, D-69120 Heidelberg, Germany.
Ann Bot. 2014 Oct;114(6):1087-97. doi: 10.1093/aob/mcu038. Epub 2014 Mar 30.
Arabinogalactan protein 31 (AGP31) is a remarkable plant cell-wall protein displaying a multi-domain organization unique in Arabidopsis thaliana: it comprises a predicted signal peptide (SP), a short AGP domain of seven amino acids, a His-stretch, a Pro-rich domain and a PAC (PRP-AGP containing Cys) domain. AGP31 displays different O-glycosylation patterns with arabinogalactans on the AGP domain and Hyp-O-Gal/Ara-rich motifs on the Pro-rich domain. AGP31 has been identified as an abundant protein in cell walls of etiolated hypocotyls, but its function has not been investigated thus far. Literature data suggest that AGP31 may interact with cell-wall components. The purpose of the present study was to identify AGP31 partners to gain new insight into its function in cell walls.
Nitrocellulose membranes were prepared by spotting different polysaccharides, which were either obtained commercially or extracted from cell walls of Arabidopsis thaliana and Brachypodium distachyon. After validation of the arrays, in vitro interaction assays were carried out by probing the membranes with purified native AGP31 or recombinant PAC-V5-6xHis. In addition, dynamic light scattering (DLS) analyses were carried out on an AGP31 purified fraction.
It was demonstrated that AGP31 interacts through its PAC domain with galactans that are branches of rhamnogalacturonan I. This is the first experimental evidence that a PAC domain, also found as an entire protein or a domain of AGP31 homologues, can bind carbohydrates. AGP31 was also found to bind methylesterified polygalacturonic acid, possibly through its His-stretch. Finally, AGP31 was able to interact with itself in vitro through its PAC domain. DLS data showed that AGP31 forms aggregates in solution, corroborating the hypothesis of an auto-assembly.
These results allow the proposal of a model of interactions of AGP31 with different cell-wall components, in which AGP31 participates in complex supra-molecular scaffolds. Such scaffolds could contribute to the strengthening of cell walls of quickly growing organs such as etiolated hypocotyls.
阿拉伯半乳聚糖蛋白31(AGP31)是一种显著的植物细胞壁蛋白,在拟南芥中呈现出独特的多结构域组织:它包含一个预测的信号肽(SP)、一个由七个氨基酸组成的短AGP结构域、一个组氨酸延伸区、一个富含脯氨酸的结构域和一个PAC(含半胱氨酸的PRP - AGP)结构域。AGP31在AGP结构域上具有与阿拉伯半乳聚糖不同的O - 糖基化模式,在富含脯氨酸的结构域上具有富含Hyp - O - Gal/Ara的基序。AGP31已被鉴定为黄化下胚轴细胞壁中的一种丰富蛋白,但迄今为止其功能尚未得到研究。文献数据表明AGP31可能与细胞壁成分相互作用。本研究的目的是鉴定AGP31的相互作用伙伴,以深入了解其在细胞壁中的功能。
通过点样不同的多糖制备硝酸纤维素膜,这些多糖要么是商业获得的,要么是从拟南芥和二穗短柄草的细胞壁中提取的。在验证阵列后,通过用纯化的天然AGP31或重组PAC - V5 - 6xHis探测膜进行体外相互作用分析。此外,对AGP31纯化组分进行动态光散射(DLS)分析。
结果表明,AGP31通过其PAC结构域与鼠李糖半乳糖醛酸聚糖I的分支半乳聚糖相互作用。这是第一个实验证据,表明作为AGP31同源物的整个蛋白质或结构域中也存在的PAC结构域可以结合碳水化合物。还发现AGP31可能通过其组氨酸延伸区结合甲基酯化的聚半乳糖醛酸。最后,AGP31能够在体外通过其PAC结构域与自身相互作用。DLS数据表明AGP31在溶液中形成聚集体,证实了自组装的假设。
这些结果提出了一个AGP31与不同细胞壁成分相互作用的模型,其中AGP31参与复杂的超分子支架。这种支架可能有助于加强快速生长器官如黄化下胚轴的细胞壁。