应用纳米标签和纳米抗体对大肠杆菌的 Z 环进行活细胞单分子成像。

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY
Current Genetics Pub Date : 2023-06-01 Epub Date: 2023-04-06 DOI:10.1007/s00294-023-01266-2
Emma Westlund, Axel Bergenstråle, Alaska Pokhrel, Helena Chan, Ulf Skoglund, Daniel O Daley, Bill Söderström
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引用次数: 0

摘要

了解蛋白质在细菌细胞中的定位位置对于理解其功能和调控至关重要。这对于参与细胞分裂的蛋白质尤为重要,这些蛋白质定位于分裂隔膜,并组装成受高度调控的复合物。利用荧光蛋白融合的超分辨率成像技术极大地促进了目前对这些复合物的了解。在这里,我们用 FtsZ 演示了使用基因融合的纳米标签(ALFA)和与 mEos3.2 融合的相应纳米抗体可在体内获得单分子 PALM 图像。该方法适用于其他细菌蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Application of nanotags and nanobodies for live cell single-molecule imaging of the Z-ring in Escherichia coli.

Application of nanotags and nanobodies for live cell single-molecule imaging of the Z-ring in Escherichia coli.

Understanding where proteins are localized in a bacterial cell is essential for understanding their function and regulation. This is particularly important for proteins that are involved in cell division, which localize at the division septum and assemble into highly regulated complexes. Current knowledge of these complexes has been greatly facilitated by super-resolution imaging using fluorescent protein fusions. Herein, we demonstrate with FtsZ that single-molecule PALM images can be obtained in-vivo using a genetically fused nanotag (ALFA), and a corresponding nanobody fused to mEos3.2. The methodology presented is applicable to other bacterial proteins.

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来源期刊
Current Genetics
Current Genetics 生物-遗传学
CiteScore
6.00
自引率
0.00%
发文量
34
审稿时长
1 months
期刊介绍: Current Genetics publishes genetic, genomic, molecular and systems-level analysis of eukaryotic and prokaryotic microorganisms and cell organelles. All articles are peer-reviewed. The journal welcomes submissions employing any type of research approach, be it analytical (aiming at a better understanding), applied (aiming at practical applications), synthetic or theoretical. Current Genetics no longer accepts manuscripts describing the genome sequence of mitochondria/chloroplast of a small number of species. Manuscripts covering sequence comparisons and analyses that include a large number of species will still be considered.
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