Summary of 13-Watabe-MolDyn

SSBD:database
SSBD:database URL
Title
-
Description
-
Relase date
2016-01-18
Updated date
2018-11-15
License
CC BY
Kind
Quantitative data, Image data based on Experiment, Simulation
Number of Datasets
6 ( Image datasets: 2, Quantitative data datasets: 4 )
Size of Datasets
151.4 GB ( Image datasets: 496.3 KB, Quantitative data datasets: 151.4 GB )

Organism(s)
D. discoideum, R. norvegicus
Strain(s)
PC-12
Protein name(s)
ERK, PTEN

Datatype
single molecule dynamics
Molecular Function (MF)
Biological Process (BP)
cellular protein localization
Cellular Component (CC)
-
Biological Imaging Method
-
XYZ Scale
XY: 414.3 nanometer/pixel, Z: 0 micrometer/slice, XY: 207.16 nanometer/pixel, Z: 0 micrometer/slice, XY: 1 micrometer, Z: 1 micrometer
T scale
0.001 second for each time interval , 1.0 second for each time interval , 0.003 second for each time interval , 0.1 second for each time interval , 1.10 microsecond for each time interval, 1.206 second for each time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Related paper(s)

Masaki Watabe, Satya N V Arjunan, Seiya Fukushima, Kazunari Iwamoto, Jun Kozuka, Satomi Matsuoka, Yuki Shindo, Masahiro Ueda, Koichi Takahashi (2015) A Computational Framework for Bioimaging Simulation., PloS one, Volume 10, Number 7, pp. e0130089

Published in 2015 (Electronic publication in July 6, 2015, midnight )

(Abstract) Using bioimaging technology, biologists have attempted to identify and document analytical interpretations that underlie biological phenomena in biological cells. Theoretical biology aims at distilling those interpretations into knowledge in the mathematical form of biochemical reaction networks and understanding how higher level functions emerge from the combined action of biomolecules. However, there still remain formidable challenges in bridging the gap between bioimaging and mathematical modeling. Generally, measurements using fluorescence microscopy systems are influenced by systematic effects that arise from stochastic nature of biological cells, the imaging apparatus, and optical physics. Such systematic effects are always present in all bioimaging systems and hinder quantitative comparison between the cell model and bioimages. Computational tools for such a comparison are still unavailable. Thus, in this work, we present a computational framework for handling the parameters of the cell models and the optical physics governing bioimaging systems. Simulation using this framework can generate digital images of cell simulation results after accounting for the systematic effects. We then demonstrate that such a framework enables comparison at the level of photon-counting units.
(MeSH Terms)

Contact
Koichi Takahashi , RIKEN , Quantitative Biology Center , Laboratory for Biochemical Simulation
Contributors
Masaki Watabe, Satya N. V. Arjunan, Seiya Fukushima, Kazunari Iwamoto, Jun Kozuka, Satomi Matsuoka, Yuki Shindo, Masahiro Ueda, Koichi Takahashi


Dataset List of 13-Watabe-MolDyn

#
Dataset ID
Kind
Size
4D View
SSBD:OMERO
Download BDML
Download Images
# 774
Datast ID Ddi_PTEN_LSCM_EXP
Dataset Kind Image data
Dataset Size 49.7 KB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 775
Datast ID Ddi_PTEN_LSCM_SIM
Dataset Kind Quantitative data
Dataset Size 9.4 GB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 776
Datast ID NA_TMR_LSCM_SIM
Dataset Kind Quantitative data
Dataset Size 9.6 GB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 777
Datast ID NA_TMR_TIRFM_SIM
Dataset Kind Quantitative data
Dataset Size 36.6 MB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 778
Datast ID Rat_ERK_LSCM_EXP
Dataset Kind Image data
Dataset Size 252.5 KB
4D view
SSBD:OMERO
Download BDML
Download Image data

# 779
Datast ID Rat_ERK_LSCM_SIM
Dataset Kind Quantitative data
Dataset Size 132.4 GB
4D view
SSBD:OMERO
Download BDML
Download Image data