D3D is a 3D reaction-diffusion simulator created by The Silver Lab at University College London (http://silverlab.org/) written in Java.
To simulate diffusion, D3D uses either an explicit finite-difference method similar to that described by Crank (1975) or a Monte Carlo algorithm for non-overlapping hard spheres that explicitly accounts for excluded volume effects (Cichocki and Hinsen, 1990).
For more information contact [email protected]
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An easy-to-use graphical interface for viewing simulation parameters, geometries, point-spread functions (PSFs), diffusants, sources and detectors.
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The ability to preview simulations in a 2D viewer.
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Functions for specifying arbitrary 3D geometries.
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Functions for specifying illumination and detection PSFs for photolysis reactions (see PSF.java) including uncaging and fluorescence recovery after photobleaching (FRAP).
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Automatic generation of log files that include nearly all simulation parameters.
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Master class functions for creating user-defined simulations (see Master.java).
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Demo initialisation classes that include several simulation examples (D3D > Project > Init).
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Functions for creating 2D projections of spherical particles for Monte Carlo simulations, including demo functions for recreating the 2D projections used in the preprint 'Validation of a stereological method for estimating particle size and density from 2D projections with high accuracy' (D3D > Project > Init > InitMC_Projection_Demo).
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Glutamate release in the synaptic cleft between cerebellar mossy fiber terminals (MFTs) and granule cell (GC) dendrites (Nielsen et al., 2004).
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Glutamate uncaging in the synaptic cleft of the cerebellar MFT, to investigate the desensitization properties of post-synaptic AMPA receptors of GCs (DiGregorio et al., 2007).
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The spatiotemporal distribution of Ca2+ in the vicinity of voltage-gate Ca2+ channel (VGCC) clusters at the calyx of Held terminal, including Ca2+ diffusion and binding with buffers and fluorescence dye, and the detection of fluorescence using a Gaussian confocal PSF (Nakamura et al., 2015; Nakamura et al., 2018).
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Brownian motion of synaptic vesicles in cerebellar MFTs, including steric interactions (Rothman et al., 2016).
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Synaptic vesicle dynamics near active zones, including connectors, tethers, docking and release (Rothman et al., 2016).
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2D projections of spherical particles in planar and thick sections (Rothman et al., 2023).
B Cichocki, K Hinsen (1990) Dynamic computer simulation of concentrated hard sphere suspensions: I. Simulation technique and mean square displacement data. Physica A 166:473–491. https://doi.org/10.1016/0378-4371(90)90068-4
J Crank (1975) The Mathematics of Diffusion. Oxford UK: Clarendon Press.
TA Nielsen, DA DiGregorio, RA Silver (2004) Modulation of glutamate mobility reveals the mechanism underlying slow-rising AMPAR EPSCs and the diffusion coefficient in the synaptic cleft. Neuron 42:757–771. https://doi.org/10.1016/j.neuron.2004.04.003
DA DiGregorio, JS Rothman, TA Nielsen, RA Silver (2007) Desensitization properties of AMPA receptors at the cerebellar mossy fiber granule cell synapse. Journal of Neuroscience 27:8344–8357. https://doi.org/10.1523/JNEUROSCI.2399-07.2007
Y Nakamura, H Harada, N Kamasawa, K Matsui, JS Rothman, R Shigemoto, RA Silver, DA DiGregorio, T Takahashi (2015) Nanoscale distribution of presynaptic Ca(2+) channels and its impact on vesicular release during development. Neuron 85:145–158. https://doi.org/10.1016/j.neuron.2014.11.019
Nakamura Y, Reva M, DiGregorio DA (2018) Variations in Ca2+ Influx Can Alter Chelator-Based Estimates of Ca2+ Channel-Synaptic Vesicle Coupling Distance. J Neurosci. 38(16):3971-3987. https://doi.org/10.1523/JNEUROSCI.2061-17.2018.
JS Rothman, L Kocsis, E Herzog, Z Nusser, RA Silver (2016) Physical determinants of vesicle mobility and supply at a central synapse. Elife. 2016 Aug 19;5. pii: e15133. https://doi.org/10.7554/eLife.15133
JS Rothman, C Borges-Merjane, N Holderith, P Jonas, RA Silver (2023) Validation of a stereological method for estimating particle size and density from 2D projections with high accuracy. PLoS One. 18(3):e0277148. https://doi.org/10.1371/journal.pone.0277148
Screnshot of a D3D Monte Carlo FRAP simulation showing mitochondria (dark grey), synaptic vesicles (green and light gray) and the illumination point-spread function (blue). See Rothman et al., 2016.