Analysis and Interpretation of Superresolution Single-Particle Trajectories

被引:21
|
作者
Holcman, D. [1 ,2 ]
Hoze, N. [3 ]
Schuss, Z. [4 ]
机构
[1] Ecole Normale Super, IBENS, Appl Math & Computat Biol, F-75231 Paris, France
[2] Univ Cambridge, Univ Cambridge Churchill Coll, Cambridge, England
[3] ETH, ETH Zentrum CHN, Inst Integrat Biol, Zurich, Switzerland
[4] Tel Aviv Univ, Dept Appl Math, IL-69978 Tel Aviv, Israel
关键词
BROWNIAN-MOTION; TRACKING; RECEPTORS; DYNAMICS; SURFACE;
D O I
10.1016/j.bpj.2015.09.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A large number (tens of thousands) of single molecular trajectories on a cell membrane can now be collected by superresolution methods. The data contains information about the diffusive motion of molecule, proteins, or receptors and here we review methods for its recovery by statistical analysis of the data. The information includes the forces, organization of the membrane, the diffusion tensor, the long-time behavior of the trajectories, and more. To recover the long-time behavior and statistics of long trajectories, a stochastic model of their nonequilibrium motion is required. Modeling and data analysis serve extracting novel biophysical features at an unprecedented spatiotemporal resolution. The review presents data analysis, modeling, and stochastic simulations applied in particular on surface receptors evolving in neuronal cells.
引用
收藏
页码:1761 / 1771
页数:11
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