论文标题
通过光热诱导的共振,细胞膜域的成像和光谱
Imaging and Spectroscopy of Domains of the Cellular Membrane by Photothermal-Induced Resonance
论文作者
论文摘要
我们使用光热诱导的共振(PTIR)成像和光谱,以谐振和非谐振模式来研究完整细胞的细胞质膜和表面。非共鸣的PTIR图像显然提供了细胞表面的丰富细节。但是,我们表明,非共鸣的图像对比不是由表面分子的红外吸收引起的,而是由尖端样本接触的力学主导。相反,可以通过调整激光的脉冲结构以限制热波穿透到表面层来选择性地获得细胞表面的光谱和图像。谐振PTIR图像揭示了大小从约20 nm到1 um范围的表面结构和域,并且与细胞质膜及其接近性有关。细胞表面的共振PTIR光谱与远场IR光谱相当,并提供了完整细胞细胞膜的IR吸收光谱的首次选择性测量。在共振PTIR图像中,信号强度以及对比度可以归因于各种因素,包括细胞表面的机械,热力学和光谱特性。尽管PTIR图像很难用光谱吸收来解释,但它们易于收集并提供独特的对比机制而无需任何外源标记。因此,它们在细胞成像和膜生物学方面提供了新的范式,可用于解决一系列关键问题,从膜脂质结构域的性质到病毒膜融合。
We use photothermal induced resonance (PTIR) imaging and spectroscopy, in resonant and non-resonant mode, to study the cytoplasmic membrane and surface of intact cells. Non-resonant PTIR images apparently provide rich details of the cell surface. However we show that non-resonant image contrast does not arise from the infrared absorption of surface molecules and is instead dominated by the mechanics of tip-sample contact. In contrast, spectra and images of the cellular surface can be selectively obtained by tuning the pulsing structure of the laser to restrict thermal wave penetration to the surface layer. Resonant PTIR images reveal surface structures and domains that range in size from about 20 nm to 1 um and are associated to the cytoplasmic membrane and its proximity. Resonant PTIR spectra of the cell surface are comparable to far-field IR spectra and provide the first selective measurement of the IR absorption spectrum of the cellular membrane of an intact cell. In resonant PTIR images, signal intensity, and therefore contrast, can be ascribed to a variety of factors, including mechanical, thermodynamic and spectroscopic properties of the cellular surface. While PTIR images are difficult to interpret in terms of spectroscopic absorption, they are easy to collect and provide unique contrast mechanisms without any exogenous labeling. As such they provide a new paradigm in cellular imaging and membrane biology and can be used to address a range of critical questions, from the nature of membrane lipid domains to viral membrane fusion.