Related Experiment Video
Updated: Jun 16, 2026

Mapping Molecular Diffusion in the Plasma Membrane by Multiple-Target Tracing (MTT)
Published on: May 27, 2012
Diffusion simulation-based fiber tracking using time-of-arrival maps: a comparison with standard methods
Sarah C Mang1, Dmitriy Logashenko, Daniel Gembris
1Section Experimental MR, Department of Neuroradiology, University Hospital, Tuebingen, Germany. s.mang@dkfz-heidelberg.de
Object:
We propose a new tracking method based on time-of-arrival (TOA) maps derived from simulated diffusion processes.
Materials And Methods:
The proposed diffusion simulation-based tracking consists of three steps that are successively evaluated on small overlapping sub-regions in a diffusion tensor field. First, the diffusion process is simulated for several time steps. Second, a TOA map is created to store simulation results for the individual time steps that are required for the tract reconstruction. Third, the fiber pathway is reconstructed on the TOA map and concatenated between neighboring sub-regions. This new approach is compared with probabilistic and streamline tracking. All methods are applied to synthetic phantom data for an easier evaluation of their fiber reconstruction quality.
Results:
The comparison of the tracking results did show severe problems for the streamline approach in the reconstruction of crossing fibers, for example. The probabilistic method was able to resolve the crossing, but could not handle strong curvature. The new diffusion simulation-based tracking could reconstruct all problematic fiber constellations.
Conclusion:
The proposed diffusion simulation-based tracking method used the whole tensor information of a neighborhood of voxels and is, therefore, able to handle problematic tracking situations better than established methods.
More Related Videos
Related Concept Videos
Protein Diffusion in the Membrane
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...

