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单颗粒追踪作为一种解决高度共定位蛋白质差异的方法。

Single particle tracking as a method to resolve differences in highly colocalized proteins.

机构信息

School of Chemistry and Biochemistry and Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, 901 Atlantic Drive, Atlanta, Georgia 30332, USA.

出版信息

Analyst. 2011 Sep 7;136(17):3527-33. doi: 10.1039/c0an00855a. Epub 2011 Jan 31.

Abstract

Single particle tracking fluorescence microscopy was used to study two late endosomal proteins, Rab7 and LAMP1, that appear to be highly colocalized in static fluorescence microscopy images. Imaging these proteins simultaneously reveals that Rab7 and LAMP1 undergo periods of separation within the cell. Single particle tracking carried out during these periods of separation shows that Rab7-vesicles have greater velocities, but undergo less efficient transport than LAMP1-vesicles. This research demonstrates the use of single particle tracking as a tool to resolve functional differences in highly colocalized proteins in intact live cells.

摘要

采用单颗粒示踪荧光显微镜研究了两种晚期内体蛋白 Rab7 和 LAMP1,它们在静态荧光显微镜图像中似乎高度共定位。同时对这些蛋白质进行成像揭示了 Rab7 和 LAMP1 在细胞内经历分离期。在这些分离期进行单颗粒示踪研究表明,Rab7 小泡的速度更快,但转运效率低于 LAMP1 小泡。这项研究证明了单颗粒示踪技术可用于解析完整活细胞中高度共定位蛋白质的功能差异。

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