首页> 外文会议>Conference on Single Molecule Spectroscopy and Imaging; 20080119-21; San Jose,CA(US) >Overcoming the depth discrimination barrier in widefield microscopes: 3D single molecule tracking with high axial accuracy
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Overcoming the depth discrimination barrier in widefield microscopes: 3D single molecule tracking with high axial accuracy

机译:克服宽视场显微镜中的深度识别障碍:具有高轴向精度的3D单分子跟踪

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Current widefield microscopy techniques are well suited for imaging fast moving single molecules in two dimensions even within cells. However, the 3D imaging of single molecules poses several technical challenges. Foremost being that in the current microscope design only one focal plane can be imaged at any given point in time. Hence single molecule tracking in a 3D environment such as a cell is problematic since the molecule can easily move out of the focal plane that is currently being imaged. Focusing devices such as piezo nano-positioners could be used to overcome this shortcoming by sequentially scanning the sample at different planes. However, these devices are typically slow and therefore may not be suitable for 3D tracking of fast moving single molecules. Aside from this, widefield microscopes suffer from poor depth discrimination capability. Therefore, there exists significant uncertainty in determining the axial location of the single molecule, especially when the molecule is close to the plane of focus. To overcome the above limitations, we have developed a new microscopy technique called multifocal plane microscopy (MUM) that can simultaneously image distinct planes within the specimen. In contrast to standard microscopes, a MUM setup exhibits significantly improved depth discrimination capability, especially close to focus, which markedly improves the accuracy with which the axial position of the single molecule can be determined. Results are presented to illustrate the applicability of MUM for 3D single molecule tracking.
机译:当前的宽视场显微镜技术非常适合在二维内甚至在细胞内对快速移动的单个分子进行成像。但是,单个分子的3D成像带来了一些技术挑战。最重要的是,在当前的显微镜设计中,在任何给定的时间点只能成像一个焦平面。因此,在诸如细胞的3D环境中跟踪单个分子是有问题的,因为该分子可以容易地移出当前正在成像的焦平面。诸如压电纳米定位器之类的聚焦装置可用于通过在不同平面上顺序扫描样品来克服这一缺点。但是,这些设备通常很慢,因此可能不适合快速移动的单个分子的3D跟踪。除此之外,宽视场显微镜还具有差的深度判别能力。因此,在确定单个分子的轴向位置时存在很大的不确定性,尤其是当该分子靠近焦点平面时。为了克服上述限制,我们开发了一种称为多焦平面显微镜(MUM)的新显微镜技术,该技术可以同时对样本中的不同平面成像。与标准显微镜相比,MUM设置具有显着改善的深度分辨能力,尤其是在焦点附近,从而显着提高了确定单个分子轴向位置的准确性。给出结果以说明MUM在3D单分子跟踪中的适用性。

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