Vahid Milad R, Chao Jerry, Kim Dongyoung, Ward E Sally, Ober Raimund J
Department of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Department of Molecular and Cellular Medicine, Texas A&M Health Science Center, College Station, TX 77843, USA.
Biomed Opt Express. 2017 Feb 6;8(3):1332-1355. doi: 10.1364/BOE.8.001332. eCollection 2017 Mar 1.
Single molecule super-resolution microscopy enables imaging at sub-diffraction-limit resolution by producing images of subsets of stochastically photoactivated fluorophores over a sequence of frames. In each frame of the sequence, the fluorophores are accurately localized, and the estimated locations are used to construct a high-resolution image of the cellular structures labeled by the fluorophores. Many methods have been developed for localizing fluorophores from the images. The majority of these methods comprise two separate steps: detection and estimation. In the detection step, fluorophores are identified. In the estimation step, the locations of the identified fluorophores are estimated through an iterative approach. Here, we propose a non-iterative state space-based localization method which combines the detection and estimation steps. We demonstrate that the estimated locations obtained from the proposed method can be used as initial conditions in an estimation routine to potentially obtain improved location estimates. The proposed method models the given image as the frequency response of a multi-order system obtained with a balanced state space realization algorithm based on the singular value decomposition of a Hankel matrix. The locations of the poles of the resulting system determine the peak locations in the frequency domain, and the locations of the most significant peaks correspond to the single molecule locations in the original image. The performance of the method is validated using both simulated and experimental data.
单分子超分辨率显微镜通过在一系列帧上生成随机光激活荧光团子集的图像,能够以亚衍射极限分辨率进行成像。在序列的每一帧中,荧光团被精确地定位,并且估计的位置被用于构建由荧光团标记的细胞结构的高分辨率图像。已经开发了许多从图像中定位荧光团的方法。这些方法中的大多数包括两个独立的步骤:检测和估计。在检测步骤中,识别荧光团。在估计步骤中,通过迭代方法估计已识别荧光团的位置。在此,我们提出一种基于状态空间的非迭代定位方法,该方法将检测和估计步骤结合在一起。我们证明,从所提出的方法获得的估计位置可以用作估计例程中的初始条件,以潜在地获得改进的位置估计。所提出的方法将给定图像建模为通过基于汉克尔矩阵奇异值分解的平衡状态空间实现算法获得的多阶系统的频率响应。所得系统极点的位置确定频域中的峰值位置,并且最显著峰值的位置对应于原始图像中的单分子位置。使用模拟数据和实验数据对该方法的性能进行了验证。