Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University.
Department of Biological Chemistry, the Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Glycobiology. 2018 Jun 1;28(6):363-373. doi: 10.1093/glycob/cwy029.
O-linked N-acetylglucosamine (O-GlcNAcylation) is an important post-translational modification on serine or threonine of proteins, mainly observed in nucleus or cytoplasm. O-GlcNAcylation regulates many cell processes, including transcription, cell cycle, neural development and nascent polypeptide chains stabilization. However, the facile identification of O-GlcNAc is a major bottleneck in O-GlcNAcylation research. Herein, we report that a lectin, Agrocybe aegerita GlcNAc-specific lectin (AANL), also reported as AAL2, can be used as a powerful probe for O-GlcNAc identification. Glycan array analyses and surface plasmon resonance (SPR) assays show that AANL binds to GlcNAc with a dissociation constant (KD) of 94.6 μM, which is consistent with the result tested through isothiocyanate (ITC) assay reported before (Jiang S, Chen Y, Wang M, Yin Y, Pan Y, Gu B, Yu G, Li Y, Wong BH, Liang Y, et al. 2012. A novel lectin from Agrocybe aegerita shows high binding selectivity for terminal N-acetylglucosamine. Biochem J. 443:369-378.). Confocal imaging shows that AANL co-localizes extensively with NUP62, a heavily O-GlcNAcylated and abundant nuclear pore glycoprotein. Furthermore, O-GlcNAc-modified peptides could be effectively enriched in the late flow-through peak from simple samples by using affinity columns Sepharose 4B-AANL or POROS-AANL. Therefore, using AANL affinity column, we identified 28 high-confidence O-linked HexNAc-modified peptides mapped on 17 proteins involving diverse cellular progresses, including transcription, hydrolysis progress, urea cycle, alcohol metabolism and cell cycle. And most importantly, major proteins and sites were not annotated in the dbOGAP database. These results suggest that the AANL lectin is a new useful tool for enrichment and identification of O-GlcNAcylated proteins and peptides.
O-连接的 N-乙酰葡萄糖胺(O-GlcNAcylation)是蛋白质丝氨酸或苏氨酸上的一种重要的翻译后修饰,主要存在于细胞核或细胞质中。O-GlcNAcylation 调节许多细胞过程,包括转录、细胞周期、神经发育和新生多肽链的稳定。然而,O-GlcNAc 的便捷鉴定是 O-GlcNAcylation 研究的主要瓶颈。在此,我们报告一种凝集素,即双孢蘑菇 GlcNAc 特异性凝集素(AANL),也被报道为 AAL2,可以用作 O-GlcNAc 鉴定的有力探针。糖组分析和表面等离子体共振(SPR)分析表明,AANL 与 GlcNAc 的解离常数(KD)为 94.6 μM,与之前报道的异硫氰酸酯(ITC)实验结果一致(Jiang S, Chen Y, Wang M, Yin Y, Pan Y, Gu B, Yu G, Li Y, Wong BH, Liang Y, et al. 2012. A novel lectin from Agrocybe aegerita shows high binding selectivity for terminal N-acetylglucosamine. Biochem J. 443:369-378.)。共聚焦成像显示,AANL 与富含 O-GlcNAc 的核孔糖蛋白 NUP62 广泛共定位。此外,通过使用亲和柱 Sepharose 4B-AANL 或 POROS-AANL,可从简单样品的后期流穿峰中有效富集 O-GlcNAc 修饰的肽段。因此,我们使用 AANL 亲和柱鉴定了 28 个高可信度的 O 连接六己糖胺修饰肽,这些肽映射到涉及多种细胞进程的 17 种蛋白质上,包括转录、水解进程、尿素循环、酒精代谢和细胞周期。最重要的是,dbOGAP 数据库中没有注释主要蛋白质和位点。这些结果表明,AANL 凝集素是一种新的有用工具,可用于 O-GlcNAc 修饰蛋白和肽的富集和鉴定。