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基于杂化纳米共轭物细胞表面自组装介导的膜蛋白/脂筏聚集的超分辨率成像与定量分析

Super-Resolution Imaging and Quantitative Analysis of Membrane Protein/Lipid Raft Clustering Mediated by Cell-Surface Self-Assembly of Hybrid Nanoconjugates.

作者信息

Hartley Jonathan M, Chu Te-Wei, Peterson Eric M, Zhang Rui, Yang Jiyuan, Harris Joel, Kopeček Jindřich

机构信息

Department of Bioengineering, University of Utah, 20 S. 2030 E., Room 108, Salt Lake City, UT 84112 (USA).

Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, 30 S. 2000 E Room 301, Salt Lake City, UT 84112 (USA).

出版信息

Chembiochem. 2015 Aug 17;16(12):1725-9. doi: 10.1002/cbic.201500278. Epub 2015 Jul 2.

Abstract

Super-resolution imaging was used to quantify organizational changes in the plasma membrane after treatment with hybrid nanoconjugates. The nanoconjugates crosslinked CD20 on the surface of malignant B cells, thereby inducing apoptosis. Super-resolution images were analyzed by using pair-correlation analysis to determine cluster size and to count the average number of molecules in the clusters. The role of lipid rafts was investigated by pre-treating cells with a cholesterol chelator and actin destabilizer to prevent lipid raft formation. Lipid raft cluster size correlated with apoptosis induction after treatment with the nanoconjugates. Lipid raft clusters had radii of ∼ 200 nm in cells treated with the hybrid nanoconjugates. Super-resolution images provided precise molecule location coordinates that could be used to determine density of bound conjugates, cluster size, and number of molecules per cluster.

摘要

超分辨率成像用于量化用混合纳米共轭物处理后质膜中的组织变化。纳米共轭物交联恶性B细胞表面的CD20,从而诱导细胞凋亡。通过使用对相关性分析来分析超分辨率图像,以确定簇大小并计算簇中分子的平均数量。通过用胆固醇螯合剂和肌动蛋白稳定剂预处理细胞以防止脂筏形成,来研究脂筏的作用。脂筏簇大小与用纳米共轭物处理后的细胞凋亡诱导相关。在用混合纳米共轭物处理的细胞中,脂筏簇的半径约为200 nm。超分辨率图像提供了精确的分子定位坐标,可用于确定结合共轭物的密度、簇大小和每个簇中的分子数量。

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