Höpfner Dorothea, Fauser Joel, Kaspers Marietta S, Pett Christian, Hedberg Christian, Itzen Aymelt
Department of Biochemistry and Signaltransduction, University Medical Center Hamburg-Eppendorf (UKE), Martinistr. 52, 20246 Hamburg, Germany.
Center for Integrated Protein Science Munich (CIPSM), Department Chemistry, Technical University of Munich, Lichtenbergstrasse 4, 85747 Garching, Germany.
iScience. 2020 Nov 13;23(12):101800. doi: 10.1016/j.isci.2020.101800. eCollection 2020 Dec 18.
AMPylation is a post-translational modification that modifies amino acid side chains with adenosine monophosphate (AMP). Recently, a role of AMPylation as a universal regulatory mechanism in infection and cellular homeostasis has emerged, driving the demand for universal tools to study this modification. Here, we describe three monoclonal anti-AMP antibodies (mAbs) from mouse that are capable of protein backbone-independent recognition of AMPylation, in denatured (western blot) as well as native (ELISA, IP) applications, thereby outperforming previously reported tools. These antibodies are highly sensitive and specific for AMP modifications, highlighting their potential as tools for new target identification, as well as for validation of known targets. Interestingly, applying the anti-AMP mAbs to various cancer cell lines reveals a previously undescribed broad and diverse AMPylation pattern. In conclusion, these anti-AMP mABs will further advance the current understanding of AMPylation and the spectrum of modified targets.
腺苷酸化是一种翻译后修饰,它用单磷酸腺苷(AMP)修饰氨基酸侧链。最近,腺苷酸化作为感染和细胞稳态中的一种普遍调节机制的作用已显现出来,这推动了对研究这种修饰的通用工具的需求。在此,我们描述了三种来自小鼠的单克隆抗AMP抗体(mAb),它们能够在变性(western印迹)以及天然(ELISA、免疫沉淀)应用中对腺苷酸化进行不依赖蛋白质骨架的识别,从而优于先前报道的工具。这些抗体对AMP修饰具有高度敏感性和特异性,突出了它们作为新靶点鉴定工具以及已知靶点验证工具的潜力。有趣的是,将抗AMP mAb应用于各种癌细胞系揭示了一种先前未描述的广泛且多样的腺苷酸化模式。总之,这些抗AMP mAb将进一步推动目前对腺苷酸化及其修饰靶点谱的理解。