Turner Linda, Berg Howard C
The Rowland Institute, Cambridge, MA, USA.
Departments of Molecular and Cellular Biology and of Physics, Harvard University, Cambridge, MA, USA.
Methods Mol Biol. 2018;1729:71-76. doi: 10.1007/978-1-4939-7577-8_7.
We describe labeling of bacteria with amino-specific or sulfhydryl-specific Alexa Fluor dyes, methods that allow visualization of flagellar filaments, even in swimming cells. Bacterial flagellar filaments are long (10 μm), but of small diameter (20 nm), and their rotation rates are high (>100 Hz), so visualization is difficult. Dark-field microscopy works well with isolated filaments, but visualization in situ is hampered by light scattered from cell bodies, which obscures short filaments or the proximal ends of long filaments. Differential interference contrast microscopy also works, but is technically difficult and suffers from a narrow depth of field and low image contrast; background subtraction and contrast enhancement are necessary. If filaments are fluorescent, they can be imaged in their entirety using standard fluorescence microscopes. For imaging in vivo, blurring can be prevented by strobing the light source or by using a camera with a fast shutter. The former method is preferred, since it minimizes bleaching.
我们描述了用氨基特异性或巯基特异性Alexa Fluor染料标记细菌的方法,这些方法能够使鞭毛丝可视化,即使是在游动的细胞中。细菌鞭毛丝很长(约10μm),但直径很小(约20nm),并且它们的旋转速度很高(>100Hz),因此可视化很困难。暗场显微镜对分离的鞭毛丝效果良好,但原位可视化受到细胞体散射光的阻碍,这会使短鞭毛丝或长鞭毛丝的近端模糊不清。微分干涉对比显微镜也可行,但技术上有难度,且景深窄、图像对比度低;需要进行背景扣除和对比度增强。如果鞭毛丝具有荧光,就可以使用标准荧光显微镜对其进行整体成像。对于体内成像,可以通过频闪光源或使用具有快速快门的相机来防止模糊。前一种方法更可取,因为它能使漂白最小化。