Department of Chemistry, University of Tennessee, 1420 Circle Drive, Knoxville, TN, 37996, USA.
Department of Microbiology, University of Tennessee, 1311 Cumberland Avenue, Knoxville, TN, 37996, USA.
Chemistry. 2023 Jul 6;29(38):e202300417. doi: 10.1002/chem.202300417. Epub 2023 May 15.
We report the use of clickable monoacylglycerol (MAG) analogs as probes for the labeling of glycerolipids during lipid metabolism. Incorporation of azide tags onto the glycerol region was pursued to develop probes that would label glycerolipids, in which the click tag would not be removed through processes including acyl chain and headgroup remodeling. Analysis of clickable MAG probes containing acyl chains of different length resulted in widely variable cell imaging and cytotoxicity profiles. Based on these results, we focused on a probe bearing a short acyl chain (C -MAG-N ) that was found to infiltrate natural lipid biosynthetic pathways to produce click-tagged versions of both neutral and phospholipid products. Alternatively, strategic blocking of the glycerol sn-3 position in probe C -MEG-N served to deactivate phospholipid tagging and focus labeling on neutral lipids. This work shows that lipid metabolic labeling profiles can be tuned based on probe structures and provides valuable tools for evaluating alterations to lipid metabolism in cells.
我们报告了可点击单酰基甘油 (MAG) 类似物在脂质代谢过程中作为甘油脂质标记物的用途。我们在甘油区域上引入叠氮标记,以开发不会通过酰基链和头部基团重塑等过程去除点击标签的探针。对含有不同长度酰基链的可点击 MAG 探针的分析导致细胞成像和细胞毒性谱广泛变化。基于这些结果,我们专注于带有短酰基链 (C-MAG-N) 的探针,该探针渗透天然脂质生物合成途径以产生中性和磷脂产物的点击标记版本。或者,探针 C-MEG-N 中甘油 sn-3 位置的策略阻断可使磷脂标记失活并将标记集中在中性脂质上。这项工作表明,可以根据探针结构调整脂质代谢标记谱,并为评估细胞中脂质代谢的改变提供有价值的工具。