Rubio Vicente, McInchak Nicholas, Fernandez Genesis, Benavides Dana, Herrera Diana, Jimenez Catherine, Mesa Haylee, Meade Jonathan, Zhang Qi, Stawikowski Maciej J
Department of Chemistry and Biochemistry, Charles E. Schmidt College of Science, Florida Atlantic University, 777 Glades Rd, Boca Raton, FL, 33431, USA.
Stiles-Nicholson Brain Institute, Florida Atlantic University, 5353 Parkside Dr, Jupiter, FL, 33458, USA.
Sci Rep. 2024 Dec 28;14(1):30777. doi: 10.1038/s41598-024-80958-2.
We present novel fluorescent cholesteryl probes (CNDs) with a modular design based on the solvatochromic 1,8-phthalimide scaffold. We have explored how different modules-linkers and head groups-affect the ability of these probes to integrate into lipid membranes and how they distribute intracellularly in mouse astrocytes and fibroblasts targeting lysosomes and lipid droplets. Each compound was assessed for its solvatochromic behavior in organic solvents and model membranes. Molecular dynamics simulations and lipid partitioning using giant unilamellar vesicles showed how these analogs behave in model membranes compared to cholesterol. Live-cell imaging demonstrated distinct staining patterns and cellular uptake behaviors, further validating the utility of these probes in biological systems. We compared the empirical results with those of BODIPY-cholesterol, a well-regarded fluorescent cholesterol analog. The internalization efficiency of fluorescent CND probes varies in different cell types and is affected mainly by the head groups. Our results demonstrate that the modular design significantly simplifies the creation of fluorescent cholesteryl probes bearing distinct spectral, biophysical, and cellular targeting features. It is a valuable toolkit for imaging in live cells, measuring cellular membrane dynamics, and studying cholesterol-related processes.
我们展示了基于溶剂致变色1,8-邻苯二甲酰亚胺支架的模块化设计的新型荧光胆固醇探针(CND)。我们研究了不同模块(连接子和头部基团)如何影响这些探针整合到脂质膜中的能力,以及它们如何在靶向溶酶体和脂滴的小鼠星形胶质细胞和成纤维细胞内分布。评估了每种化合物在有机溶剂和模型膜中的溶剂致变色行为。使用巨型单层囊泡进行的分子动力学模拟和脂质分配显示了这些类似物与胆固醇相比在模型膜中的行为。活细胞成像展示了不同的染色模式和细胞摄取行为,进一步验证了这些探针在生物系统中的实用性。我们将实验结果与备受认可的荧光胆固醇类似物BODIPY-胆固醇的结果进行了比较。荧光CND探针的内化效率在不同细胞类型中有所不同,并且主要受头部基团的影响。我们的结果表明,模块化设计显著简化了具有独特光谱、生物物理和细胞靶向特征的荧光胆固醇探针的创建。它是用于活细胞成像、测量细胞膜动力学以及研究胆固醇相关过程的有价值工具包。