AbstractFour different tandem EGFPs were constructed to elucidate the nuclear microenvironment by quantifying its diffusional properties in both aqueous solution and the nuclei of living cells. Diffusion of tandem EGFP was dependent on the length of the protein as a rod-like molecule or molecular ruler in solution. On the other hand, we found two kinds of mobility, fast diffusional mobility and much slower diffusional mobility depending on cellular compartments in living cells. Diffusion in the cytoplasm and the nucleoplasm was mainly measured as fast diffusional mobility. In contrast, diffusion in the nucleolus was complex and mainly much slower diffusional mobility, although both the fast and the slow diffusional mobilities were dependent...
Fluorescence microphotolysis was used to measure nucleocytoplasmic flux in single rat hepatocytes fo...
AbstractThe nucleus is the center of direction and coordination of the cell's metabolic and reproduc...
<p>(A–B') Sample micrographs: HEp-2 cells were incubated with fluorescent COOH-PS [YO] NPs for 30 mi...
AbstractFour different tandem EGFPs were constructed to elucidate the nuclear microenvironment by qu...
No methods proposed thus far have the capability to measure overall molecular flow in the nucleus of...
No methods proposed thus far have the capability to measure overall molecular flow in the nucleus of...
AbstractThe NPC is the portal for the exchange of proteins, mRNA, and ions between nucleus and cytop...
AbstractThe nuclear envelope (NE) defines the nuclear compartment, and nuclear pore complexes (NPCs)...
We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This metho...
We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This metho...
<p>FRAP-based estimation of diffusion coefficient values (A) and mobile fraction (B) of eGFP and NCp...
© 2002 The Rockefeller University PressAfter being released from transcription sites, messenger ribo...
Fluorescence recovery after photobleaching (FRAP) can help unveil subtle dynamical and biochemical p...
<p>The figure shows the diffusion coefficients of the eGFP oligomers (blue squares) plotted against ...
The process of autophagy involves the formation of autophagosomes, double-membrane structures that e...
Fluorescence microphotolysis was used to measure nucleocytoplasmic flux in single rat hepatocytes fo...
AbstractThe nucleus is the center of direction and coordination of the cell's metabolic and reproduc...
<p>(A–B') Sample micrographs: HEp-2 cells were incubated with fluorescent COOH-PS [YO] NPs for 30 mi...
AbstractFour different tandem EGFPs were constructed to elucidate the nuclear microenvironment by qu...
No methods proposed thus far have the capability to measure overall molecular flow in the nucleus of...
No methods proposed thus far have the capability to measure overall molecular flow in the nucleus of...
AbstractThe NPC is the portal for the exchange of proteins, mRNA, and ions between nucleus and cytop...
AbstractThe nuclear envelope (NE) defines the nuclear compartment, and nuclear pore complexes (NPCs)...
We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This metho...
We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This metho...
<p>FRAP-based estimation of diffusion coefficient values (A) and mobile fraction (B) of eGFP and NCp...
© 2002 The Rockefeller University PressAfter being released from transcription sites, messenger ribo...
Fluorescence recovery after photobleaching (FRAP) can help unveil subtle dynamical and biochemical p...
<p>The figure shows the diffusion coefficients of the eGFP oligomers (blue squares) plotted against ...
The process of autophagy involves the formation of autophagosomes, double-membrane structures that e...
Fluorescence microphotolysis was used to measure nucleocytoplasmic flux in single rat hepatocytes fo...
AbstractThe nucleus is the center of direction and coordination of the cell's metabolic and reproduc...
<p>(A–B') Sample micrographs: HEp-2 cells were incubated with fluorescent COOH-PS [YO] NPs for 30 mi...