期刊论文详细信息
JOURNAL OF MOLECULAR BIOLOGY 卷:433
Line-FRAP, A Versatile Method to Measure Diffusion Rates In Vitro and In Vivo
Article
Dey, Debabrata1  Marciano, Shir1  Nunes-Alves, Ariane2,3  Kiss, Vladimir1  Wade, Rebecca C.2,3,4  Schreiber, Gideon1 
[1] Weizmann Inst Sci, Dept Biomol Sci, Rehovot, Israel
[2] Heidelberg Inst Theoret Studies, Mol & Cellular Modeling Grp, Schloss Wolfsbrunnenweg 35, D-69118 Heidelberg, Germany
[3] Heidelberg Univ, Ctr Mol Biol ZMBH, DKFZ ZMBH Alliance, Neuenheimer Feld 282, D-69120 Heidelberg, Germany
[4] Heidelberg Univ, Interdisciplinary Ctr Sci Comp IWR, Neuenheimer Feld 205, Heidelberg, Germany
关键词: protein diffusion;    FRAP;    eukaryotic cell;    prokaryotic cell;    macromolecular crowding;   
DOI  :  10.1016/j.jmb.2021.166898
来源: Elsevier
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【 摘 要 】

The crowded cellular milieu affect molecular diffusion through hard (occluded space) and soft (weak, nonspecific) interactions. Multiple methods have been developed to measure diffusion coefficients at physiological protein concentrations within cells, each with its limitations. Here, we show that Line-FRAP, combined with rigours data analysis, is able to determine diffusion coefficients in a variety of environments, from in vitro to in vivo. The use of Line mode greatly improves time resolution of FRAP data acquisition, from 20-100 Hz in the classical mode to 800 Hz in the line mode. This improves data analysis, as intensity and radius of the bleach at the first post-bleach frame is critical. We evaluated the method on different proteins labelled chemically or fused to YFP in a wide range of environments. The diffusion coefficients measured in HeLa and in E. coli were similar to 2.5-fold and 15-fold slower than in buffer, and were comparable to previously published data. Increasing the osmotic pressure on E. coli further decreases diffusion, to the point at which proteins virtually stop moving. The method presented here, which requires a confocal microscope equipped with dual scanners, can be applied to study a large range of molecules with different sizes, and provides robust results in a wide range of environments and protein concentrations for fast diffusing molecules. (C) 2021 Elsevier Ltd. All rights reserved.

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