Membrane staining and phospholipid tracking in Pseudomonas aeruginosa PAO1 using the phosphatidylcholine mimic propargyl-choline.

Access microbiology Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI:10.1099/acmi.0.000690.v3
Chris L B Graham, Jack Bryant, David I Roper, Manuel Banzhaf
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引用次数: 0

Abstract

The use of membrane-specific dyes for in vivo fluorescent microscopy is commonplace. However, most of these reagents are non-specific and cannot track specific lipid species movement, instead often acting as non-covalent lipid-associated probes or requiring the uptake of whole lipids and acyl tails into the membrane. This issue has been solved in eukaryotic cell biology by the use of click-chemistry-liable phospholipid headgroup pulse labels. Here, we describe a method for in vivo phospholipid labelling by fluorescent imaging in Pseudomonas aeruginosa using a phosphatidylcholine mimic, 'propargyl-choline' (PCho). This click-chemistry-liable headgroup mimic is visible by microscopy and allows the covalent labelling of lipids. Fluorescence of the cell membranes, visible in heterogeneous patches, is dependent on PCho concentration and is localized in the membrane fraction of cells, demonstrating that it is suitable for membrane labelling and cell imaging.

利用磷脂酰胆碱模拟物丙炔胆碱对铜绿假单胞菌PAO1进行膜染色和磷脂跟踪。
在体内荧光显微镜中使用膜特异性染料是司空见惯的。然而,这些试剂大多是非特异性的,不能追踪特定的脂质运动,而通常作为非共价脂质相关探针或需要将整个脂质和酰基尾部摄取到膜中。在真核细胞生物学中,这个问题已经通过使用易于点击化学的磷脂头群脉冲标签得到了解决。在这里,我们描述了一种使用磷脂酰胆碱模拟物“丙炔胆碱”(PCho)的铜绿假单胞菌荧光成像的体内磷脂标记方法。这种点击化学倾向的头群模拟物在显微镜下是可见的,并允许脂质的共价标记。细胞膜的荧光,在异质斑块中可见,依赖于PCho浓度,并定位于细胞的膜部分,表明它适用于膜标记和细胞成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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