Spector Jeffrey O, Vemu Annapurna, Roll-Mecak Antonina
Cell Biology and Biophysics Unit, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, Bethesda, MD, USA.
Methods Mol Biol. 2020;2101:39-51. doi: 10.1007/978-1-0716-0219-5_4.
Microtubules are dynamic non-covalent mesoscopic polymers. Their dynamic behavior is essential for cell biological processes ranging from intracellular transport to cell division and neurogenesis. Fluorescence microscopy has been the method of choice for monitoring microtubule dynamics in the last two decades. However, fluorescent microtubules are prone to photodamage that alters their dynamics, and the fluorescent label itself can affect microtubule properties. Dark-field imaging is a label-free technique that can generate high signal-to-noise, low-background images of microtubules at high acquisition rates without the photobleaching inherent to fluorescence microscopy. Here, we describe how to image in vitro microtubule dynamics using dark-field microscopy. The ability to image microtubules label-free allows the investigation of the dynamic properties of non-abundant tubulin species where fluorescent labeling is not feasible, free from the confounding effects arising from the addition of fluorescent labels.
微管是动态的非共价介观聚合物。它们的动态行为对于从细胞内运输到细胞分裂和神经发生等细胞生物学过程至关重要。在过去二十年中,荧光显微镜一直是监测微管动态的首选方法。然而,荧光微管容易受到光损伤,从而改变其动态,并且荧光标记本身会影响微管特性。暗场成像为一种无标记技术,它能够以高采集速率生成微管的高信噪比、低背景图像,且不存在荧光显微镜固有的光漂白问题。在此,我们描述如何使用暗场显微镜对体外微管动态进行成像。无标记成像微管的能力使得在荧光标记不可行的情况下,能够研究非丰富微管蛋白种类的动态特性,且不受添加荧光标记所产生的混杂效应影响。