a hidden markov model for single particle tracks quantifies dynamic interactions between lfa-1 and the actin cytoskeleton单粒子轨道的隐马尔科夫模型量化动态lfa-1和肌动蛋白细胞骨架之间的相互作用.pdfVIP

a hidden markov model for single particle tracks quantifies dynamic interactions between lfa-1 and the actin cytoskeleton单粒子轨道的隐马尔科夫模型量化动态lfa-1和肌动蛋白细胞骨架之间的相互作用.pdf

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a hidden markov model for single particle tracks quantifies dynamic interactions between lfa-1 and the actin cytoskeleton单粒子轨道的隐马尔科夫模型量化动态lfa-1和肌动蛋白细胞骨架之间的相互作用

A Hidden Markov Model for Single Particle Tracks Quantifies Dynamic Interactions between LFA-1 and the Actin Cytoskeleton 1 2 1 Raibatak Das *, Christopher W. Cairo , Daniel Coombs 1 Department of Mathematics and Institute of Applied Mathematics, University of British Columbia, Vancouver, British Columbia, Canada, 2 Alberta Ingenuity Centre for Carbohydrate Science, Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada Abstract The extraction of hidden information from complex trajectories is a continuing problem in single-particle and single-molecule experiments. Particle trajectories are the result of multiple phenomena, and new methods for revealing changes in molecular processes are needed. We have developed a practical technique that is capable of identifying multiple states of diffusion within experimental trajectories. We model single particle tracks for a membrane-associated protein interacting with a homogeneously distributed binding partner and show that, with certain simplifying assumptions, particle trajectories can be regarded as the outcome of a two-state hidden Markov model. Using simulated trajectories, we demonstrate that this model can be used to identify the key biophysical parameters for such a system, namely the diffusion coefficients of the underlying states, and the rates of transition between them. We use a stochastic optimization scheme to compute maximum likelihood estimates of these parameters. We have applied this analysis to single-particle trajectories of the integrin receptor lymphocyte function-associated antigen-1 (LFA-1) on live T cells. Our analysis reveals that the diffusion of LFA-1 is indeed approximately two-state, and is characterized by large changes in cytoskeletal interactions upon cellular activation. Citation: Das R, Cairo

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