A Multifunctional Probe for Visualization of the Nanoscale Distribution of Cholesterol in Cells by Expansion Microscopy

IF 13.7 Q1 CHEMISTRY, MULTIDISCIPLINARY
Gang Wen, Dominic A. Helmerich, Lisa Behringer-Pließ, Markus Sauer
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Abstract

Unraveling the nanoscale distribution of small molecules in cells is of central importance for the understanding of cellular functions and the development of drugs. However, particularly the visualization of lipids such as cholesterol—a central compound of cell membranes—with high spatial resolution remains challenging because they cannot be efficiently immobilized for super-resolution microscopy investigations. Here we developed an azido- and amino-modified cholesterol probe that can be efficiently fixed and labeled with fluorophores by click chemistry. In combination with expansion microscopy, its cellular localization and interaction with other cellular proteins can be precisely determined in fixed cells at varying time points after addition. Our approach allows us to detect the endocytic pathway of cholesterol with unprecedented spatial resolution and shows that cholesterol is efficiently ingested in endocytic vesicles and accumulates as cholesterol aggregates with an average size of ∼37 nm in late endosomes and lysosomes, respectively.

Abstract Image

用扩增显微镜观察细胞内胆固醇纳米分布的多功能探针
揭示细胞中小分子的纳米级分布对于理解细胞功能和开发药物至关重要。然而,特别是脂质(如胆固醇-细胞膜的中心化合物)的高空间分辨率可视化仍然具有挑战性,因为它们不能有效地固定在超分辨率显微镜下进行研究。在这里,我们开发了一种叠氮和氨基修饰的胆固醇探针,可以通过点击化学有效地固定和标记荧光团。结合扩增显微镜,可以在添加后的不同时间点精确测定其在固定细胞中的细胞定位和与其他细胞蛋白的相互作用。我们的方法使我们能够以前所未有的空间分辨率检测胆固醇的内吞途径,并表明胆固醇在内吞囊泡中有效摄入,并在内核体和溶酶体中分别以平均大小为~ 37 nm的胆固醇聚集体积累。
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来源期刊
CiteScore
17.40
自引率
0.00%
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审稿时长
7 weeks
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