Poganik Jesse R, Aye Yimon
Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland.
Front Aging Neurosci. 2020 Feb 7;12:1. doi: 10.3389/fnagi.2020.00001. eCollection 2020.
With a lipid-rich environment and elevated oxygen consumption, the central nervous system (CNS) is subject to intricate regulation by lipid-derived electrophiles (LDEs). Investigations into oxidative damage and chronic LDE generation in neural disorders have spurred the development of tools that can detect and catalog the gamut of LDE-adducted proteins. Despite these advances, deconstructing the precise consequences of individual protein-specific LDE modifications remained largely impossible until recently. In this perspective, we first overview emerging toolsets that can decode electrophile-signaling events in a protein/context-specific manner, and how the accumulating mechanistic insights brought about by these tools have begun to offer new means to modulate pathways relevant to multiple sclerosis (MS). By surveying the latest data surrounding the blockbuster MS drug dimethyl fumarate that functions through LDE-signaling-like mechanisms, we further provide a vision for how chemical biology tools probing electrophile signaling may be leveraged toward novel interventions in CNS disease.
由于富含脂质的环境和较高的氧消耗,中枢神经系统(CNS)受到脂质衍生亲电试剂(LDEs)的复杂调控。对神经疾病中氧化损伤和慢性LDE生成的研究推动了能够检测和编目LDE加合蛋白范围的工具的开发。尽管取得了这些进展,但直到最近,解析单个蛋白质特异性LDE修饰的确切后果在很大程度上仍然是不可能的。从这个角度来看,我们首先概述了能够以蛋白质/背景特异性方式解码亲电试剂信号事件的新兴工具集,以及这些工具带来的越来越多的机制见解如何开始提供调节与多发性硬化症(MS)相关途径的新方法。通过审视围绕通过类似LDE信号机制发挥作用的重磅MS药物富马酸二甲酯的最新数据,我们进一步展望了探索亲电试剂信号的化学生物学工具如何用于中枢神经系统疾病的新型干预。