4.4 Article

Cega: a single particle segmentation algorithm to identify moving particles in a noisy system

期刊

MOLECULAR BIOLOGY OF THE CELL
卷 32, 期 9, 页码 931-941

出版社

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E20-11-0744

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资金

  1. Center for Engineering MechanoBiology National Science Foundation Science and Technology Center [CMMI:15-48571]
  2. National Institutes of Health [RM1 GM136511, R35 GM126950]

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Improvements in particle tracking algorithms are necessary for analyzing the mobility of biological molecules in complex systems. A new approach using the Kullback-Leibler divergence has shown significant improvements in identifying moving particles and background signals, leading to better SPT capabilities.
Improvements to particle tracking algorithms are required to effectively analyze the motility of biological molecules in complex or noisy systems. A typical single particle tracking (SPT) algorithm detects particle coordinates for trajectory assembly. However, particle detection filters fail for data sets with low signal-to-noise levels. When tracking molecular motors in complex systems, standard techniques often fail to separate the fluorescent signatures of moving particles from background signal. We developed an approach to analyze the motility of kinesin motor proteins moving along the microtubule cytoskeleton of extracted neurons using the Kullback-Leibler divergence to identify regions where there are significant differences between models of moving particles and background signal. We tested our software on both simulated and experimental data and found a noticeable improvement in SPT capability and a higher identification rate of motors as compared with current methods. This algorithm, called Cega, for find the object, produces data amenable to conventional blob detection techniques that can then be used to obtain coordinates for downstream SPT processing. We anticipate that this algorithm will be useful for those interested in tracking moving particles in complex in vitro or in vivo environments.

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