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首页> 外文期刊>Acta biochimica Polonica >Analytical ultracentrifugation as a tool in the studies of aggregation of the fluorescent marker, Enhanced Green Fluorescent Protein
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Analytical ultracentrifugation as a tool in the studies of aggregation of the fluorescent marker, Enhanced Green Fluorescent Protein

机译:分析超速离心作为荧光标记物聚集研究的工具,增强绿色荧光蛋白

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Enhanced green fluorescent protein (EGFP) is a fluorescent marker used in bio-imaging applications, including as an indicator of folding or aggregation of a fused partner. However, the limited maturation, low folding efficiency, and presence of non-fluorescent states of EGFP can influence the interpretation of experimental data. To measure aggregation associated with de novo folding of EGFP from a high GdnHCl concentration, the analytical ultracentrifugation method was used. Absorption detection at 280 nm allowed to monitor the presence of monomers and aggregated forms. Fluorescence detection enabled the observation of only properly folded molecules with a functional chromophore. The results showed intensive aggregation of EGFP in low concentrations of GdnHCl with a continuous distribution of aggregated forms. The properly folded monomers with mature chromophore were fluorescent, while the conglomerates of EGFP molecules were not. These facts are essential for a proper interpretation of data obtained with EGFP labelling.
机译:增强的绿色荧光蛋白(EGFP)是生物成像应用中使用的荧光标记物,包括作为融合伴侣的折叠或聚集的指示剂。然而,有限的成熟,低折叠效率和EGFP的非荧光状态的存在可以影响实验数据的解释。为了测量与Novo折叠EGFP与高GDNHCL浓度相关的聚集,使用分析超速离心方法。吸收检测在280nm处允许监测单体和聚集形式的存在。荧光检测使仅具有功能性发色团的仅折叠的分子。结果表明,在低浓度的GDNHCL中,具有综合分布的聚集形式的强浓度聚集。具有成熟发色团的正确折叠的单体是荧光的,而EGFP分子的砾岩不是。这些事实对于使用EGFP标签获得的数据进行适当的解释至关重要。

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