2009 Annual Report Vol.37 - 中研院物理研究所 - Academia Sinica
2009 Annual Report Vol.37 - 中研院物理研究所 - Academia Sinica
2009 Annual Report Vol.37 - 中研院物理研究所 - Academia Sinica
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Gelatin scaffold in red and fibroblast cells are labelled with phalladin in green and<br />
DAPI in blue.<br />
(5). Single Molecule Studies of Highly Confined Biological Macromolecules<br />
The idea of confining long-chain macromolecules to surfaces has always<br />
intrigued polymer scientists. Although lots of efforts have been made in the studies of<br />
bulk characters of confined polymer chains, our knowledge on these molecules at<br />
microscopic level is still very limited. Our research interests are mainly focused on<br />
understanding the static and dynamic behaviors of highly confined polymer molecules.<br />
Two model systems, the densely end-tethered polymer brushes and the fully adsorbed<br />
polymers on glass-supported lipid membranes, have been intensively studied from the<br />
single molecule aspect for past years. A novel assay has been developed to construct<br />
high density end-grafted polymer layers on solid-liquid interface through<br />
end-tethering DNA molecules at grafting density above 25 molecules/ Rg 2 . We have<br />
demonstrated the first single molecule study of polymer brushes with the fluorescent<br />
microscopy technique. We are able to visualize the conformation and the dynamics of<br />
individual polymer molecule in this model polymer coated layer, and understand the<br />
detailed response of the polymer brush to the shear flow. Our very recent finding also<br />
shows the diffusivity of small molecules in such an entropy-driven brush layer could<br />
be strongly retarded. This finding might be relevant to how this tailor-made surface<br />
protects the substrate. Through monitoring the adsorption and the relaxation of DNA<br />
molecules on the glass-supported charged lipid membranes, the response of individual<br />
chain-like macromolecule to the sudden variation of the system geometry has been<br />
studied. Following a rapid adsorption, a multi-stage anomalous swelling governed by<br />
the interplay between the polymer topology and the dynamics of the charged lipid<br />
molecules on the membrane has been observed for the first time. Our analysis also<br />
shows a novel spatial-temporal pattern of the adsorbed DNA molecule at scales of a<br />
38