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Surface-enhanced Raman scattering-based detection of the interactions between the essential cell division FtsZ protein and bacterial membrane elements

机译:基于表面增强拉曼散射的基本细胞分裂FtsZ蛋白与细菌膜元件之间相互作用的检测

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摘要

Surface-enhanced Raman scattering (SERS) spectroscopy has been applied to detect the interaction of the FtsZ protein from Escherichia coli, an essential component of the bacterial division machinery, with either a soluble variant of the ZipA protein (that provides membrane tethering to FtsZ) or the bacterial membrane (containing the full-length ZipA naturally incorporated), on silver-coated polystyrene micrometer-sized beads. The engineered microbeads were used not only to support the bilayers but also to offer a stable support with a high density of SERS hot spots, allowing the detection of ZipA structural changes linked to the binding of FtsZ. These changes were different upon incubating the coated beads with FtsZ polymers (GTP form) as compared to oligomers (GDP form) and more pronounced when the plasmonic sensors were coated with natural bacterial membranes.
机译:表面增强拉曼散射(SERS)光谱已用于检测大肠杆菌中FtsZ蛋白(细菌分裂机制的重要组成部分)与ZipA蛋白的可溶变体(提供与FtsZ的膜束缚)的相互作用或细菌膜(包含天然掺入的全长ZipA)在镀银的聚苯乙烯微米级微珠上。工程化的微珠不仅用于支撑双层,还用于以高密度的SERS热点提供稳定的支撑,从而可以检测与FtsZ结合相关的ZipA结构变化。与低聚物(GDP形式)相比,用FtsZ聚合物(GTP形式)孵育包被的珠子后,这些变化有所不同,当等离激元传感器被天然细菌膜包被时,这些变化更为明显。

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