Laboratory for Cell Function Dynamics
"Why bio-imaging, i.e. real time fluorescence imaging?" Currently, this is a topic of great interest in the bioscience community. Many molecules involved in signal transduction have been identified, and the hierarchy among those molecules has also been elucidated. It is not uncommon to see a signal transduction diagram in which arrows are used to link molecules to show enzyme reactions and intermolecular interactions. To obtain a further understanding of a signal transduction system, however, the diagram must contain the three axes in space as well as a fourth dimension, time, because all events are controlled ingeniously in space and time. Since the isolation of green fluorescent protein (GFP) from the bioluminescent jellyfish in 1992 and later with its relatives, researchers have been awaiting the development of a tool, which enables the direct visualization of biological functions. This has been increasingly enhanced by the marriage of GFP with fluorescence resonance energy transfer (FRET) or fluorescence cross-correlation spectroscopy (FCCS), and is further expanded upon by the need for "post-genomic analyses." It is not my intent to discourage the trend seeking the visualization of biological function. I would like to propose that it is time to evaluate the true asset of "bio-imaging" for its potential and limitations in order to utilize and truly benefit from this novel technique.
- Development of a new microscopy system
- Development of fluorescent indicators for various cellular events using novel fluorescent protein
- Local and physiological Ca2+ imaging
- January 25 ,2011
- Effects of anti-cancer drugs reassessed using fluorescence imaging technology
- November 17, 2009
- Embryogenesis propagation and differentiation patterns of live fish exposed to full view
- December 20, 2008
- Differential silhouetting of the cell cycle specific to either S/G2/M a new visualizing technology of the cellular proliferation process
- July 12, 2008
- Incorporating a novel fluorescence protein to develop a high sensitivity membrane potential probe
- June 24, 2008
- Elucidating the molecular mechanism of photochromism of a fluorescent protein 'Drompa' with NMR analysis of its dark-structure, instead of X-ray structural analysis
- February 8, 2008
- Color-coded mouse genes reveal hidden story on cell cycle
- Sakaue-Sawano A, Kobayashi T, Ohtawa K, Miyawaki A.:
"Drug-induced cell cycle modulation leading to cell-cycle arrest, nuclear mis-segregation, or endoreplication."
BMC Cell Biology, 12:2 (2011) - Miyawaki A.:
"Imaging: Visualizing a neuronal handshake."
Nat. Chem. Biol., 6 (12): 885-886 (2010). - Tsutsui H, Higashijima SI, Miyawaki A, Okamura Y.:
"Visualizing Voltage Dynamics in Zebrafish Heart."
J Physiol. 588(Pt 12): 2017-2021 (2010). - Tsutsui H, Shimizu H, Mizuno H, Nukina N, Furuta T, Miyawaki A.:
"The E1 mechanism in photo-induced β-elimination reactions for green-to red conversion of fluorescent proteins."
Chemistry & Biology, 16(11): 1140-1147 (2009). - Sugiyama M, Sakaue-Sawano A, Iimura T, Fukami K, Kitaguchi T, Kawakami K, Okamoto H, Higashijima S, Miyawaki A.:
"Illuminating cell-cycle progression in the developing zebrafish embryo."
Proc. Natl. Acad. Sci. USA., 106 (49): 20812-20817 (2008). - Miyawaki A.:
"Great expectations."
Science, 326 (5951): 339 (2009). - Shimozono S, Tsutsui H, Miyawaki A.:
"Diffusion of Large Molecules into Assembling Nuclei Revealed Using."
Biophys. J. 97 (5): 1288-1294 (2009). - Sakaue-Sawano A, Ohtawa K, Hama H, Kawano M, Ogawa M, Miyawaki A.:
"Tracing the Silhouette of Individual Cells in S/G2/M Phases with Fluorescence"
Chemistry & Biology, 15: 1243-1248 (2008). - Tsutsui H, Karasawa S, Okamura Y, Miyawaki A:
"Improving membrane voltage measurements using FRET with new fluorescent proteins"
Nature Methods, 5: 683-685 (2008). - Mizuno H, Kumar Mal T, Wälchli M, Kikuchi A, Fukano T, Ando R, Jeyakanthan J, Taka J, Shiro Y, Ikura M, Miyawaki A.:
"Light-dependent regulation of structural flexibility in a photochromic fluorescent protein"
Proc. Natl. Acad. Sci. USA., 105: 9927-9932 (2008).

