论文标题
立体黑场干涉法:一种用于单分子亚纳光力光谱的多功能定位方法和单细胞的3D换行
Stereo Darkfield Interferometry : a versatile localization method for subnanometer force spectroscopy of single molecules and 3D-tracking of single cells
论文作者
论文摘要
长期以来,诸如PSF工程或evanscent Field Imaging之类的超级分类3D跟踪已长期用于跟踪微粒并增强单分子力光谱测量的吞吐量。但是,当前方法呈现两个缺点。首先,与光学镊子或AFM相比,它们缺乏精度。其次,信号对位置的依赖性很复杂,因此需要耗时的校准步骤。 在这里,我们引入了一种新的光学技术,该技术绕过这两个问题,并允许对稀释粒子进行简单,多功能和高效的3D跟踪,同时在所有三个空间方向上提供子纳米框架到框架的精度。原理是将立体镜和干涉法结合,以使Z(轴向)位置是通过两个干涉水平模式之间的距离来测量的。这种立体镜技术的线性性减轻了对查找表的需求,而结构化干涉模式则增强了精度。另一方面,此PSF的扩展空间足迹可最大程度地提高每个框架检测到的光子数量,而无需花哨的摄像头,也不需要复杂的硬件。因此,由于它的简单性和多功能性,我们认为SDI(立体声Darkfield干涉法)技术有可能显着增强3D跟踪的传播。 通过磁镊子,我们证明了该技术对各种单分子测量的效率。特别是我们证明了涉及轴向步骤短达1 nm的两态动力学的精确定量。然后,我们证明可以将SDI直接嵌入商业目标中,从而提供了一种跟踪3D中多个单个单元格的方法。
Super-resolutive 3D tracking, such as PSF engineering or evanescent field imaging has long been used to track microparticles and to enhance the throughput of single molecules force spectroscopic measurements. However, current methods present two drawbacks. First, they lack precision compared with optical tweezers or AFM. Second, the dependence of their signal upon the position is complex creating the need for a time-consuming calibration step. Here, we introduce a new optical technique that circumvents both issues and allows for a simple, versatile and efficient 3D tracking of diluted particles while offering a sub-nanometer frame-to-frame precision in all three spatial directions. The principle is to combine stereoscopy and interferometry, such that the z (axial) position is measured through the distance between two interferometric fringe patterns. The linearity of this stereoscopy technique alleviates the need for lookup tables while the structured interferometric pattern enhances precision. On the other hand, the extended spatial footprint of this PSF maximizes the number of photons detected per frame without the need of fancy cameras, nor the need for complex hardware. Hence, thanks to its simplicity and versatility, we believe that SDI (Stereo Darkfield Interferometry) technology has the potential to significantly enhance the spreading of 3D tracking. We demonstrate the efficiency of this technique on various single-molecule measurements thanks to magnetic tweezers. In particular we demonstrate the precise quantification of two-state dynamics involving axial steps as short as 1 nm. We then show that SDI can be directly embedded in a commercial objective providing a means to track multiple single cells in 3D .